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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/README.rst Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,24 @@ +FALCO Amplicon Analysis Pipeline & Galaxy wrapper +======================================== + +FALCO variant-caller is part of the Amplicon Analysis Pipeline (AAP). + +The typical workflow is as follows: +* paired-end amplicon sequencing +* merge pairs (so only overlapping pairs are included) +* map the single read fastq with BWA +* perform variant calling with FALCO +* create (html) report of the results + +FALCO uses samtools and straight-forward statistics to determine wether a +potential variant is likely a (technical) artifact or not. + +Input / Output + +Input of the caller is a BAM file, output VCF + + +Bug Reports & other questions +============================= + +Issues can be reported via http://www.tgac.nl/
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco-call.sh Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,123 @@ +#!/bin/bash +TOOLDIR="$( cd "$( dirname "${BASH_SOURCE[0]}" )" && pwd )" + +echo "Started FALCO calling" + +## ---------- +## Variables setup ($1 contains the bash config file path) +## ---------- +source $1 + +## ---------- +## make sure all is ok +## ---------- +if [ ! -f $REF_FILE".fai" ] +then + echo "No FAI index (fai) found for reference fasta [$REF_FILE]" + exit "No FAI index (fai) found for reference fasta [$REF_FILE]" +fi + +## ---------- +## set params +## ---------- +if [[ $filter_file != 'None' && $filter_file != '' ]] # Galaxy default is "None" for some reason +then + FILTER_PARAM=" --filter "$filter_file +else + FILTER_PARAM="" +fi + +if [[ $manifest_file != 'None' && $manifest_file != 'None' ]] # Galaxy default is "None" for some reason +then + MANIFEST_PARAM=" --manifest "$manifest_file +else + MANIFEST_PARAM="" +fi + +## name of file in galaxy not always set so will use a user-set job_name instead +#bam_base=`echo $bam_name | sed 's#.bam$##' - ` +bam_base=$job_name + +## ---------- +## Status / debug +## ---------- +DEBUG=1 +if [ $DEBUG ] +then + DBS="[INFO] " + echo $DBS"FILTER: "$filter_file + echo $DBS"MANIFEST: "$manifest_file + echo $DBS"REF FILE: "$REF_FILE + echo $DBS"DB KEY: "$DB_KEY + echo $DBS"REF SRC: "$REF_SOURCE + echo $DBS"BAM FILE: "$bam_file + echo $DBS"BAM NAME: "$bam_name + echo $DBS"BAM BASE: "$bam_base + echo $DBS"OUT PATH: "$out_path +fi + +## ---------- +## create output files dir +## ---------- +mkdir $out_path + +## ---------- +## running analysis +## ---------- +echo "[INFO] Starting variant calling" +## NOTE: if $FILTER_PARAM is set it includes the param name (--filter) +## NOTE: if $MANIFEST_PARAM is set it includes the param name (--manifest) +CALL_STRING="$TOOLDIR/falco/bin/falco --bam $bam_file --output $bam_base --ref $REF_FILE $FILTER_PARAM $MANIFEST_PARAM" +echo "[INFO] "$CALL_STRING +perl $CALL_STRING +echo "[INFO] done with variant calling" + + +## ---------- +## create index html for main galaxy output +## ---------- +echo "<!DOCTYPE html>" >> $html_out +echo "<html>" >> $html_out +echo "<head>" >> $html_out +echo "<style>" >> $html_out +echo " body{ padding: 0px 20px; }" >> $html_out +echo " h1{ color: red; }" >> $html_out +echo " table{ border: 1px solid black; padding: 5px }" >> $html_out +echo "</style>" >> $html_out +echo "</head>" >> $html_out +echo "<body>" >> $html_out +echo " <h1>FALCO</h1>" >> $html_out +echo " <p>This page is way to get output files that are not implemented in galaxy history, it is not intended to be a user-friendly way of displaying anything ;)</p>" >> $html_out +#echo " <a href=\"index.html\">HTML</a>" >> $html_out +echo " <table><tbody>" >> $html_out +for file in *.vcf *.txt *stderr *stdout +#for file in * +do + lineCount=`wc -l $file | cut -f 1 -d " "` + echo " <tr><td><a href=\"$file\">$file</a> has $lineCount lines</td></tr>" >> $html_out + echo " <tr><td> --> " `head -1 $file` "</td></tr>" >> $html_out +done +echo " </tbody></table>" >> $html_out +echo "</body>" >> $html_out +echo "</html>" >> $html_out + +## ---------- +## creating galaxy history outputs +## ---------- +#cp 'index.html' $html_out # this is the overview of samples html +#cp $bam_base'.html' $out_path/'out.html' # this is the sample html +cp $bam_base'.falco.vcf' $vcf_out +cp $bam_base'.qc.ann.qual.txt' $qc_ann_qual_out +cp $bam_base'.qc2.ann.txt' $qc2_ann_txt_out +cp $bam_base'.qc.targets.txt' $qc_targets_txt_out + +## ---------- +## copy files to keep to output path +## ---------- +#cp -r ./$bam_base/*png $out_path/$bam_base/ +#cp -r ./* $out_path +cp *.vcf $out_path; cp *.txt $out_path; cp *_std* $out_path + +## ---------- +echo "END falco sh" +exit 0
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco-filter-report.sh Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,120 @@ +#!/bin/bash +TOOLDIR="$( cd "$( dirname "${BASH_SOURCE[0]}" )" && pwd )" + +echo "Started FALCO calling" + +## ---------- +## Variables setup ($1 contains the bash config file path) +## ---------- +source $1 + +## ---------- +## make sure all is ok +## ---------- +#if [ ! -f $REF_FILE".fai" ] +#then +# echo "No FAI index (fai) found for reference fasta [$REF_FILE]" +# exit "No FAI index (fai) found for reference fasta [$REF_FILE]" +#fi + +## ---------- +## set params +## ---------- +if [[ $vcf2_file != 'None' && $vcf2_file != '' ]] # Galaxy default is "None" for some reason +then + VCF2_PARAM=" --vcfOther "$vcf2_file +else + VCF2_PARAM="" +fi + +# if [[ $manifest_file != 'None' && $manifest_file != 'None' ]] # Galaxy default is "None" for some reason +# then +# MANIFEST_PARAM=" --manifest "$manifest_file +# else +# MANIFEST_PARAM="" +# fi + +## name of file in galaxy not always set so will use a user-set job_name instead +#bam_base=`echo $bam_name | sed 's#.bam$##' - ` +vcf_base=$job_name +sample_html_file=$vcf_base'.html' + +## ---------- +## Status / debug +## ---------- +DEBUG=1 +# if [ $DEBUG ] +# then +# DBS="[INFO] " +# echo $DBS"FILTER: "$filter_file +# echo $DBS"MANIFEST: "$manifest_file +# echo $DBS"REF FILE: "$REF_FILE +# echo $DBS"DB KEY: "$DB_KEY +# echo $DBS"REF SRC: "$REF_SOURCE +# echo $DBS"BAM FILE: "$bam_file +# echo $DBS"BAM NAME: "$bam_name +# echo $DBS"BAM BASE: "$bam_base +# echo $DBS"OUT PATH: "$out_path +# fi + +## ---------- +## create output files dir +## ---------- +mkdir $out_path + +## ---------- +## running analysis +## ---------- +echo "[INFO] Starting FALCO reporting" +CMD_STRING="$TOOLDIR/falco/bin/falco-filter-report --vcf $vcf_file --output $vcf_base --qc_ann_qual_txt $qc_ann_qual_file --qc2_ann_txt $qc2_ann_txt_file --qc_targets_txt $qc_targets_txt_file $VCF2_PARAM" +echo "[INFO] "$CMD_STRING +perl $CMD_STRING +echo "[INFO] done with FALCO reporting" + + +## ---------- +## create index html for main galaxy output +## ---------- +echo "<!DOCTYPE html>" >> $html_out +echo "<html>" >> $html_out +echo "<head>" >> $html_out +echo "<style>" >> $html_out +echo " body{ padding: 0px 20px; }" >> $html_out +echo " h1{ color: red; }" >> $html_out +echo " table{ border: 1px solid black; padding: 5px }" >> $html_out +echo "</style>" >> $html_out +echo "</head>" >> $html_out +echo "<body>" >> $html_out +echo " <h1>FALCO</h1>" >> $html_out +echo " <a href=\"$sample_html_file\">RESULTS</a>" >> $html_out +#echo " <p>This page is way to get output files that are not implemented in galaxy history, it is not intended to be a user-friendly way of displaying anything ;)</p>" >> $html_out +#echo " <a href=\"index.html\">HTML</a>" >> $html_out +#echo " <table><tbody>" >> $html_out +#for file in *.vcf *.txt *stderr *stdout +#for file in * +#do +# lineCount=`wc -l $file | cut -f 1 -d " "` +# echo " <tr><td><a href=\"$file\">$file</a> has $lineCount lines</td></tr>" >> $html_out +# echo " <tr><td> --> " `head -1 $file` "</td></tr>" >> $html_out +#done +#echo " </tbody></table>" >> $html_out +echo "</body>" >> $html_out +echo "</html>" >> $html_out + +## ---------- +## creating galaxy history outputs +## ---------- +#cp 'index.html' $html_out # this is the overview of samples html +cp $sample_html_file $out_path # this is the sample html +#cp $vcf_base'.html' $html_out # this is the sample html + +## ---------- +## copy files to keep to output path +## ---------- +#cp -r ./$bam_base/*png $out_path/$bam_base/ +cp -r ./* $out_path +#cp *.vcf $out_path; cp *.txt $out_path; cp *_std* $out_path + +## ---------- +echo "END falco sh" +exit 0
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/README Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,33 @@ +Usage: + +falco + +input: +- bam file +- manifest file +- ref + fai +- locifilt +- manifest + +output: +- *.vcf file +- *.qc.ann.txt -> catalog of each assayed bp +- *.qc2.ann.txt -> catalog of transitions +- *.qc.targets.txt -> amplicon centered information, eg depth, start/end positions. + +example: + +OUTBASE="HCT116-TEST" + +## variant calling +falco --bam data/HCT-116/HCT116.bam --output $OUTBASE --ref genome.fa + +file1=$OUTBASE".qc.ann.qual.txt" +file2=$OUTBASE".qc2.ann.txt" +file3=$OUTBASE".qc.targets.txt" +file4=$OUTBASE".res.filtered.tsv" + +## variant filtering and reporting +falco-filter-report --vcf snpeff.vcf --output $OUTBASE --qc_ann_qual_txt $file1 --qc2_ann_txt $file2 --qc_targets_txt $file3 --res_filtered_tsv $file4 + +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/bin/falco Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,75 @@ +#!/usr/bin/perl + +use strict; +use Cwd 'abs_path'; +use Getopt::Long; +use File::Basename; + +my $absPath = abs_path($0); +my $dn = dirname($absPath); + +# Set options + +my $bam; +my $ref = "$dn/../ref/hg19/hg19.fa"; +my $locifilt = "$dn/../ref/filters/filter.tsv"; +my $manifest = "$dn/../ref/TSACP/TruSeq_Amplicon_Cancer_Panel_Manifest_AFP1_PN15032433.txt"; +my $base = $bam; + +GetOptions ( + "bam=s" => \$bam, + "ref=s" => \$ref, + "filter=s" => \$locifilt, + "manifest=s" => \$manifest, + "output=s" => \$base, +) +or die("Error in command line arguments\n"); + +## sanity checks +unless ( -f $ref ){ + print STDERR "Genome Reference file not found [$ref]\n"; + exit 1; +} +unless ( -f $ref.'.fai' ){ + print STDERR "Genome Reference index file not found [$ref\.fai]\n"; + exit 1; +} + + +# Set paths to external script +# TODO make modules + +my $perAmpliconAnalysis = "$dn/../lib/perl/perAmpliconAnalysis.pl"; +my $addQual = "$dn/../lib/R/addQual.R"; +my $func = "$dn/../lib/R/func.R"; +my $qcFilt = "$dn/../lib/perl/qcFilt.pl"; +my $qc2vcf = "$dn/../lib/perl/qc2vcf.pl"; + +# Check Rscript +my $rscript = `which Rscript`; +chomp $rscript; +if ($rscript !~ /Rscript$/) { + print STDERR "No Rscript present in PATH\n"; + exit 1; +} + +# Check samtools +my $samtools = `which samtools`; +chomp $samtools; +if ($samtools !~ /samtools$/) { + print STDERR "No samtools present in PATH\n"; + exit 1; +} + +print STDOUT localtime() . " [$$] $perAmpliconAnalysis $bam $ref $manifest $base $samtools\n"; +system("$perAmpliconAnalysis $bam $ref $manifest $base $samtools"); + +print STDOUT localtime() . " [$$] $rscript $addQual $base.qc.ann.txt $base.qc.ann.qual.txt $func $locifilt\n"; +system("$rscript $addQual $base.qc.ann.txt $base.qc.ann.qual.txt $func $locifilt"); + +print STDOUT localtime() . " [$$] $qcFilt $base.qc.ann.qual.txt $base\n"; +system("$qcFilt $base.qc.ann.qual.txt $base"); + +print STDOUT localtime() . " [$$] $qc2vcf $base.qc.ann.qual.filt.txt > $base.falco.vcf\n"; +system("$qc2vcf $base.qc.ann.qual.filt.txt > $base.falco.vcf"); +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/bin/falco-filter-report Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,93 @@ +#!/usr/bin/perl +use strict; +use Cwd 'abs_path'; +use Getopt::Long; +use File::Basename; + +my $absPath = abs_path($0); +my $dir = dirname($absPath); +my $lib = "$dir/../lib/"; + +my $vcf2tsv = "$lib/perl/vcf2tsv.pl"; +my $spliteff = "$lib/perl/splitEff.pl"; +my $filter = "$lib/perl/filter.pl"; +my $plotPng = "$lib/R/plotsPng.R"; +my $mkReport = "$lib/perl/mkHtmlReportGalaxy.pl"; + +my $locifilt = "$dir/../ref/filters/filter.tsv"; +my $manifest = "$dir/../ref/TSACP/TruSeq_Amplicon_Cancer_Panel_Manifest_AFP1_PN15032433.txt"; + +my $canonicals = "$dir/../ref/TSACP/canonicals.tsv"; +my $clinvar = "$dir/../ref/filters/clinvar_00-latest.f.vcf"; +my $cosmic = "$dir/../ref/filters/CosmicCodingMuts_v64_26032013_noLimit_wgs.f.vcf"; +my $cosmicNC = "$dir/../ref/filters/CosmicNonCodingVariants_v64_26032013_noLimit_wgs.f.vcf"; + +my $base = undef; +my $vcf = undef; +my $vcfOther = undef; +my $noFilt = undef; +my $noPlot = undef; + +my $qc_ann_qual_txt = undef; +my $qc2_ann_txt = undef +my $qc_targets_txt = undef; + +GetOptions ( + "vcf=s" => \$vcf, + "vcfOther=s" => \$vcfOther, + "output=s" => \$base, + "clinvar=s" => \$clinvar, + "cosmic=s" => \$cosmic, + "cosmicNC=s" => \$cosmicNC, + "noFilt" => \$noFilt, + "noPlot" => \$noPlot, + "qc_ann_qual_txt=s" => \$qc_ann_qual_txt, + "qc2_ann_txt=s" => \$qc2_ann_txt, + "qc_targets_txt=s" => \$qc_targets_txt, +) +or die("Error in command line arguments\n"); + +## sanity checks +die( "No base name provided [-output]\n" ) unless defined($base) and $base ne ''; +die( "No VCF file provided [-vcf]\n" ) unless defined($vcf) and -f $vcf; +die( "Missing input [-qc_ann_qual_txt]\n" ) unless defined($qc_ann_qual_txt) and -f $qc_ann_qual_txt; +die( "Missing input [-qc2_ann_txt]\n" ) unless defined($qc2_ann_txt) and -f $qc2_ann_txt; +die( "Missing input [-qc_targets_txt]\n" ) unless defined($qc_targets_txt) and -f $qc_targets_txt; +die( "Required file does not exists [$canonicals]\n" ) unless -f $canonicals; +die( "Required file does not exists [$clinvar]\n" ) unless -f $clinvar; +die( "Required file does not exists [$cosmic]\n" ) unless -f $cosmic; +die( "Required file does not exists [$cosmicNC]\n" ) unless -f $cosmicNC; + + +## Rscript check +my $rscript = `which Rscript`; +chomp $rscript; +if ($rscript !~ /Rscript$/) { + print STDERR "No Rscript present in PATH\n"; + exit 1; +} + +## FILTERING +print STDOUT localtime() . " [$$] converting vcf to tsv\n"; +system( "$vcf2tsv $vcf > $base\.tsv" ); + +print STDOUT localtime() . " [$$] splitting vcf columns\n"; +system( "$spliteff $base\.tsv Falco >> $base\.res\.tsv" ); + +if ( defined($vcfOther) ){ + print STDOUT localtime() . " [$$] converting vcf to tsv\n"; + system( "$vcf2tsv $vcf > $base\.Other\.tsv" ); + print STDOUT localtime() . " [$$] splitting vcf columns\n"; + system( "$spliteff $base\.Other\.tsv Other >> $base\.res\.tsv" ); +} + +print STDOUT localtime() . " [$$] filtering data\n"; +system( "$filter $base\.res\.tsv $canonicals $clinvar $cosmic $cosmicNC > $base\.res\.filtered\.tsv" ); + +## PLOTTING +print STDOUT localtime() . " [$$] Creating plots\n"; +system( "Rscript $plotPng $qc_ann_qual_txt $qc2_ann_txt $qc_targets_txt $base\.res\.filtered\.tsv $clinvar $locifilt $base" ); + +## REPORTING +print STDOUT localtime() . " [$$] Creating HTML report\n"; +system( "perl $mkReport $base $qc_targets_txt" );
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/R/addQual.R Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,21 @@ +#!/usr/bin/Rscript +args <- commandArgs(T) +qcFile <- args[1] +output <- args[2] +funcR <- args[3] +lociFiltFile <- args[4] + +read.delim(lociFiltFile, header=F) -> lociFiltD +lociFilt <- paste(paste("chr", lociFiltD[,1], sep=""), lociFiltD[,2], sep=":") + +source(funcR) +read.delim(qcFile, header=T) -> qc + +#addQual(qc) -> qc.qual +addQualTransCor(qc, lociFilt) -> qc.qual +#addQualVarCor(qc) -> qc.qual + +write.table(qc.qual, output, row.names=F, col.names=T, quote=F, sep="\t") +#write.table(qc[selection,], output, row.names=F, col.names=T, quote=F, sep="\t") + +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/R/func.R Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,575 @@ +#!/usr/bin/Rscript +#args <- commandArgs(T) +#qcFile <- args[1] +#output <- args[2] + +#read.delim(qcFile, header=T) -> qc + +addQual <- function(qc) { + +qc$del <- as.character(as.vector(qc$del)) +qc$ins <- as.vector(qc$ins) +qc$pVal <- 1 +qc$pValAdj <- 1 +#qc$pValPois <- 1 +qc$qScore <- 0 +qc$qScoreI <- 0 +qc$qScoreD <- 0 + +pVal.I <- rep(1, nrow(qc)) +pVal.D <- rep(1, nrow(qc)) + +delSel <- qc$del != "." +data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[delSel]), "\\|")), ":")), ncol=2, byrow=T)) -> dels +dels$ln <- nchar(as.vector(dels$X1)) +colnames(dels) <- c("seq", "occ", "ln") +delPees <- ppois(1:50, mean(rep(dels$ln, dels$occ)), lower.tail=F) + +insSel <- qc$ins != "." +data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[insSel]), "\\|")), ":")), ncol=2, byrow=T)) -> inss +inss$ln <- nchar(as.vector(inss$X1)) +colnames(inss) <- c("seq", "occ", "ln") +insPees <- ppois(1:50, mean(rep(dels$ln, dels$occ)), lower.tail=F) + +# Calculate errorrate per amplicon +amps <- unique(qc$amp) +for (i in amps) { + #print(i) + sel <- qc$amp == i + prob <- sum(qc$nVar[sel]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) + #prob <- median(qc$nVar[sel] / (qc$nRef[sel] + qc$nVar[sel])) + pees <- pbinom(qc$nVar[sel], qc$nRef[sel] + qc$nVar[sel], prob, lower.tail=F) + qc$pVal[sel] <- pees +# pois <- ppois(qc$nVar[sel], (qc$nRef + qc$nVar) * prob, lower.tail=F) +# qc$pValPois[sel] <- pois + + # Seperate for indel/deletion events + selDels <- delSel & sel + if (sum(selDels) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[selDels]), "\\|")), ":")), ncol=2, byrow=T)) -> dels2 + dels2$ln <- nchar(as.vector(dels2$X1)) + colnames(dels2) <- c("seq", "occ", "ln") + dels2$occ <- as.numeric(as.vector(dels2$occ)) + } + for (j in which(selDels)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[j]), "\\|")), ":")), ncol=2, byrow=T)) -> dels + dels$ln <- nchar(as.vector(dels$X1)) + colnames(dels) <- c("seq", "occ", "ln") + dels$occ <- as.numeric(as.vector(dels$occ)) + #dels$pDel <- delPees[as.integer(dels$ln)] + #dels$pVal <- ppois(as.numeric(dels$occ), dels$pDel, lower.tail=F) + dels$pDel <- sapply(dels$ln, function(x) {sum(dels2$occ[dels2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + dels$pVal <- pbinom(dels$occ, qc$dp[j], dels$pDel, lower.tail=F) + dels$Q <- -10 * log10(dels$pVal) + + high <- order(dels$occ, -dels$Q, decreasing=T)[1] + qc$del[j] <- paste(dels$seq[high], dels$occ[high], sep=":") + qc$qScoreD[j] <- dels$Q[high] + pVal.D[j] <- dels$pVal[high] + } + selIns <- insSel & sel + if (sum(selIns) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[selIns]), "\\|")), ":")), ncol=2, byrow=T)) -> inss2 + inss2$ln <- nchar(as.vector(inss2$X1)) + colnames(inss2) <- c("seq", "occ", "ln") + inss2$occ <- as.numeric(as.vector(inss2$occ)) + } + for (j in which(selIns)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[j]), "\\|")), ":")), ncol=2, byrow=T)) -> inss + inss$ln <- nchar(as.vector(inss$X1)) + colnames(inss) <- c("seq", "occ", "ln") + inss$occ <- as.numeric(as.vector(inss$occ)) + #inss$pIns <- insPees[as.integer(inss$ln)] + #inss$pVal <- ppois(as.numeric(inss$occ), inss$pIns, lower.tail=F) + inss$pIns <- sapply(inss$ln, function(x) {sum(inss2$occ[inss2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + inss$pVal <- pbinom(inss$occ, qc$dp[j], inss$pIns, lower.tail=F) + inss$Q <- -10 * log10(inss$pVal) + + high <- order(inss$occ, -inss$Q, decreasing=T)[1] + qc$ins[j] <- paste(inss$seq[high], inss$occ[high], sep=":") + qc$qScoreI[j] <- inss$Q[high] + pVal.I[j] <- inss$pVal[high] + } + #print(sum(-10 * log10(pees) > 100)) + #print(sum(qc$qScoreI[selIns] > 100)) + #print(sum(qc$qScoreD[selDels] > 100)) +} + +p.adjust(qc$pVal) -> qc$pValAdj +-10 * log(p.adjust(pVal.I)) -> qc$qScoreI +-10 * log(p.adjust(pVal.D)) -> qc$qScoreD +qc$qScore <- -10 * log10(qc$pValAdj) +#qc$qScore[qc$pValAdj == 0] <- 1000 +qc$qScore[qc$qScore > 1000] <- 1000 +qc$qScoreI[qc$qScoreI > 1000] <- 1000 +qc$qScoreD[qc$qScoreD > 1000] <- 1000 +qsel <- (qc$qScore >= 100 & qc$nVar >= 10) | (qc$qScoreI >= 200) | (qc$qScoreD >= 200) +dpfilt <- as.numeric(qc$dp) >= 100 +#varfilt <- as.numeric(qc$nVar) >= 10 + +selection <- qsel & dpfilt + +print(paste("Filtered out: ", sum(!selection), sep="")) +print(paste("Variants selected: ", sum(selection), sep="")) +return(qc) +} + +addQualTransCor <- function(qc, lociFilt) { + + +# lociFilt contains snp, cosmic and clinvar positions + +qc$del <- as.character(as.vector(qc$del)) +#qc$del <- as.character(as.vector(qc$del)) +qc$ins <- as.character(as.vector(qc$ins)) +qc$pVal <- 1 +qc$pValAdj <- 1 +#qc$pValPois <- 1 +qc$qScore <- 0 +qc$qScoreI <- 0 +qc$qScoreD <- 0 + +pVal.I <- rep(1, nrow(qc)) +pVal.D <- rep(1, nrow(qc)) + +rle(as.vector(qc$ntRef)) -> srle +hompols <- srle$lengths >= 5 +homPosS <- cumsum(srle$lengths)[hompols] +homPosE <- cumsum(srle$lengths)[which(hompols) - 1] +homFilt <- rep(F, nrow(qc)) +homFilt[homPosS] <- T +homFilt[homPosE] <- T + +delSel <- qc$del != "." & !homFilt +if (sum(delSel > 0)) { + + +data.frame(matrix(unlist(strsplit(unlist(strsplit(qc$del[delSel], "\\|")), ":")), ncol=2, byrow=T)) -> dels +dels$ln <- nchar(as.vector(dels$X1)) +colnames(dels) <- c("seq", "occ", "ln") +delPees <- ppois(1:50, mean(rep(dels$ln, dels$occ)), lower.tail=F) +} + +insSel <- qc$ins != "." & !homFilt +if (sum(insSel) > 0) { +data.frame(matrix(unlist(strsplit(unlist(strsplit(qc$ins[insSel], "\\|")), ":")), ncol=2, byrow=T)) -> inss +inss$ln <- nchar(as.vector(inss$X1)) +colnames(inss) <- c("seq", "occ", "ln") +insPees <- ppois(1:50, mean(rep(inss$ln, inss$occ)), lower.tail=F) +} +# Calculate transition bias + + +#calcTransCor(qc) -> pCor +globalProb <- sum(qc$nVar) / (sum(qc$nRef) + sum(qc$nVar)) +# Calculate errorrate per amplicon +amps <- unique(qc$amp) +for (i in amps) { + #print(i) + sel <- qc$amp == i + prob1 <- sum(qc$nVar[sel]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) + prob <- prob1 * calcTransCor(qc[sel,], lociFilt) + pees <- pbinom(qc$nVar[sel], qc$nRef[sel] + qc$nVar[sel], prob , lower.tail=F) + qc$pVal[sel] <- pees +# pois <- ppois(qc$nVar[sel], (qc$nRef + qc$nVar) * prob, lower.tail=F) +# qc$pValPois[sel] <- pois + + # Seperate for indel/deletion events + selDels <- delSel & sel + if (sum(selDels) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[selDels]), "\\|")), ":")), ncol=2, byrow=T)) -> dels2 + dels2$ln <- nchar(as.vector(dels2$X1)) + colnames(dels2) <- c("seq", "occ", "ln") + dels2$occ <- as.numeric(as.vector(dels2$occ)) + + for (j in which(selDels)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[j]), "\\|")), ":")), ncol=2, byrow=T)) -> dels + dels$ln <- nchar(as.vector(dels$X1)) + colnames(dels) <- c("seq", "occ", "ln") + dels$occ <- as.numeric(as.vector(dels$occ)) + #dels$pDel <- delPees[as.integer(dels$ln)] + #dels$pVal <- ppois(as.numeric(dels$occ), dels$pDel, lower.tail=F) + dels$pDel <- sapply(dels$ln, function(x) {sum(dels2$occ[dels2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + dels$pVal <- pbinom(dels$occ, qc$dp[j], dels$pDel, lower.tail=F) + dels$Q <- -10 * log10(dels$pVal) + + high <- order(dels$occ, -dels$Q, decreasing=T)[1] + qc$del[j] <- paste(dels$seq[high], dels$occ[high], sep=":") + qc$qScoreD[j] <- dels$Q[high] + pVal.D[j] <- dels$pVal[high] + } + } + selIns <- insSel & sel + if (sum(selIns) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[selIns]), "\\|")), ":")), ncol=2, byrow=T)) -> inss2 + inss2$ln <- nchar(as.vector(inss2$X1)) + colnames(inss2) <- c("seq", "occ", "ln") + inss2$occ <- as.numeric(as.vector(inss2$occ)) + + for (j in which(selIns)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[j]), "\\|")), ":")), ncol=2, byrow=T)) -> inss + inss$ln <- nchar(as.vector(inss$X1)) + colnames(inss) <- c("seq", "occ", "ln") + inss$occ <- as.numeric(as.vector(inss$occ)) + #inss$pIns <- insPees[as.integer(inss$ln)] + #inss$pVal <- ppois(as.numeric(inss$occ), inss$pIns, lower.tail=F) + inss$pIns <- sapply(inss$ln, function(x) {sum(inss2$occ[inss2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + inss$pVal <- pbinom(inss$occ, qc$dp[j], inss$pIns, lower.tail=F) + inss$Q <- -10 * log10(inss$pVal) + + high <- order(inss$occ, -inss$Q, decreasing=T)[1] + qc$ins[j] <- paste(inss$seq[high], inss$occ[high], sep=":") + qc$qScoreI[j] <- inss$Q[high] + pVal.I[j] <- inss$pVal[high] +} } + #print(sum(-10 * log10(pees) > 100)) + #print(sum(qc$qScoreI[selIns] > 100)) + #print(sum(qc$qScoreD[selDels] > 100)) +} + +p.adjust(qc$pVal) -> qc$pValAdj +-10 * log(p.adjust(pVal.I)) -> qc$qScoreI +-10 * log(p.adjust(pVal.D)) -> qc$qScoreD +qc$qScore <- -10 * log10(qc$pValAdj) +#qc$qScore[qc$pValAdj == 0] <- 1000 +qc$qScore[qc$qScore > 1000] <- 1000 +qc$qScoreI[qc$qScoreI > 1000] <- 1000 +qc$qScoreD[qc$qScoreD > 1000] <- 1000 +qsel <- (qc$qScore >= 100 & qc$nVar >= 10) | (qc$qScoreI >= 200) | (qc$qScoreD >= 200) +dpfilt <- as.numeric(qc$dp) >= 100 +#varfilt <- as.numeric(qc$nVar) >= 10 + +selection <- qsel & dpfilt + +print(paste("Filtered out: ", sum(!selection), sep="")) +print(paste("Variants selected: ", sum(selection), sep="")) +return(qc) +} + + +addQualVarCor <- function(qc) { +# Corrected for variant occurence + +qc$del <- as.character(as.vector(qc$del)) +qc$ins <- as.vector(qc$ins) +qc$pVal <- 1 +qc$pValAdj <- 1 +#qc$pValPois <- 1 +qc$qScore <- 0 +qc$qScoreI <- 0 +qc$qScoreD <- 0 + +pVal.I <- rep(1, nrow(qc)) +pVal.D <- rep(1, nrow(qc)) + +delSel <- qc$del != "." +data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[delSel]), "\\|")), ":")), ncol=2, byrow=T)) -> dels +dels$ln <- nchar(as.vector(dels$X1)) +colnames(dels) <- c("seq", "occ", "ln") +delPees <- ppois(1:50, mean(rep(dels$ln, dels$occ)), lower.tail=F) + +insSel <- qc$ins != "." +data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[insSel]), "\\|")), ":")), ncol=2, byrow=T)) -> inss +inss$ln <- nchar(as.vector(inss$X1)) +colnames(inss) <- c("seq", "occ", "ln") +insPees <- ppois(1:50, mean(rep(dels$ln, dels$occ)), lower.tail=F) + +# Calculate base bias per run +sum(qc$nA[grepl("A", qc$ntRef, ignore.case=T)]) -> refA +sum(qc$nA[!grepl("A", qc$ntRef, ignore.case=T)]) -> varA +sum(qc$nC[grepl("C", qc$ntRef, ignore.case=T)]) -> refC +sum(qc$nC[!grepl("C", qc$ntRef, ignore.case=T)]) ->varC +sum(qc$nG[grepl("G", qc$ntRef, ignore.case=T)]) -> refG +sum(qc$nG[!grepl("G", qc$ntRef, ignore.case=T)]) -> varG +sum(qc$nT[grepl("T", qc$ntRef, ignore.case=T)]) -> refT +sum(qc$nT[!grepl("T", qc$ntRef, ignore.case=T)]) -> varT + +varA / (refA + varA) -> errA +varC / (refC + varC) -> errC +varG / (refG + varG) -> errG +varT / (refT + varT) -> errT +c(errA, errC, errG, errT) / mean(c(errA, errC, errG, errT)) -> errACGT + +errMat <- qc[,9:12] +errMat[grepl("A", qc$ntRef, ignore.case=T),1] <- 0 +errMat[grepl("C", qc$ntRef, ignore.case=T),2] <- 0 +errMat[grepl("G", qc$ntRef, ignore.case=T),3] <- 0 +errMat[grepl("T", qc$ntRef, ignore.case=T),4] <- 0 + +pCor <- rep(1, nrow(qc)) +pCor[grepl("^A", qc$ntVar, ignore.case=T)] <- errACGT[1] +pCor[grepl("^C", qc$ntVar, ignore.case=T)] <- errACGT[2] +pCor[grepl("^G", qc$ntVar, ignore.case=T)] <- errACGT[3] +pCor[grepl("^T", qc$ntVar, ignore.case=T)] <- errACGT[4] + +# Calculate errorrate per amplicon +amps <- unique(qc$amp) +for (i in amps) { + #print(i) + sel <- qc$amp == i + prob <- sum(qc$nVar[sel]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) + #prob <- median(qc$nVar[sel] / (qc$nRef[sel] + qc$nVar[sel])) + pees <- pbinom(qc$nVar[sel], qc$nRef[sel] + qc$nVar[sel], prob * pCor[sel], lower.tail=F) + qc$pVal[sel] <- pees +# pois <- ppois(qc$nVar[sel], (qc$nRef + qc$nVar) * prob, lower.tail=F) +# qc$pValPois[sel] <- pois + + # Seperate for indel/deletion events + selDels <- delSel & sel + if (sum(selDels) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[selDels]), "\\|")), ":")), ncol=2, byrow=T)) -> dels2 + dels2$ln <- nchar(as.vector(dels2$X1)) + colnames(dels2) <- c("seq", "occ", "ln") + dels2$occ <- as.numeric(as.vector(dels2$occ)) + } + for (j in which(selDels)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$del[j]), "\\|")), ":")), ncol=2, byrow=T)) -> dels + dels$ln <- nchar(as.vector(dels$X1)) + colnames(dels) <- c("seq", "occ", "ln") + dels$occ <- as.numeric(as.vector(dels$occ)) + #dels$pDel <- delPees[as.integer(dels$ln)] + #dels$pVal <- ppois(as.numeric(dels$occ), dels$pDel, lower.tail=F) + dels$pDel <- sapply(dels$ln, function(x) {sum(dels2$occ[dels2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + dels$pVal <- pbinom(dels$occ, qc$dp[j], dels$pDel, lower.tail=F) + dels$Q <- -10 * log10(dels$pVal) + + high <- order(dels$occ, -dels$Q, decreasing=T)[1] + qc$del[j] <- paste(dels$seq[high], dels$occ[high], sep=":") + qc$qScoreD[j] <- dels$Q[high] + pVal.D[j] <- dels$pVal[high] + } + selIns <- insSel & sel + if (sum(selIns) > 0) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[selIns]), "\\|")), ":")), ncol=2, byrow=T)) -> inss2 + inss2$ln <- nchar(as.vector(inss2$X1)) + colnames(inss2) <- c("seq", "occ", "ln") + inss2$occ <- as.numeric(as.vector(inss2$occ)) + } + for (j in which(selIns)) { + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.vector(qc$ins[j]), "\\|")), ":")), ncol=2, byrow=T)) -> inss + inss$ln <- nchar(as.vector(inss$X1)) + colnames(inss) <- c("seq", "occ", "ln") + inss$occ <- as.numeric(as.vector(inss$occ)) + #inss$pIns <- insPees[as.integer(inss$ln)] + #inss$pVal <- ppois(as.numeric(inss$occ), inss$pIns, lower.tail=F) + inss$pIns <- sapply(inss$ln, function(x) {sum(inss2$occ[inss2$ln == x]) / (sum(qc$nRef[sel]) + sum(qc$nVar[sel])) }) + inss$pVal <- pbinom(inss$occ, qc$dp[j], inss$pIns, lower.tail=F) + inss$Q <- -10 * log10(inss$pVal) + + high <- order(inss$occ, -inss$Q, decreasing=T)[1] + qc$ins[j] <- paste(inss$seq[high], inss$occ[high], sep=":") + qc$qScoreI[j] <- inss$Q[high] + pVal.I[j] <- inss$pVal[high] + } + #print(sum(-10 * log10(pees) > 100)) + #print(sum(qc$qScoreI[selIns] > 100)) + #print(sum(qc$qScoreD[selDels] > 100)) +} + +p.adjust(qc$pVal) -> qc$pValAdj +-10 * log(p.adjust(pVal.I)) -> qc$qScoreI +-10 * log(p.adjust(pVal.D)) -> qc$qScoreD +qc$qScore <- -10 * log10(qc$pValAdj) +#qc$qScore[qc$pValAdj == 0] <- 1000 +qc$qScore[qc$qScore > 1000] <- 1000 +qc$qScoreI[qc$qScoreI > 1000] <- 1000 +qc$qScoreD[qc$qScoreD > 1000] <- 1000 +qsel <- (qc$qScore >= 100 & qc$nVar >= 10) | (qc$qScoreI >= 200) | (qc$qScoreD >= 200) +dpfilt <- as.numeric(qc$dp) >= 100 +#varfilt <- as.numeric(qc$nVar) >= 10 + +selection <- qsel & dpfilt + +print(paste("Filtered out: ", sum(!selection), sep="")) +print(paste("Variants selected: ", sum(selection), sep="")) +return(qc) +} + +#addQual(qc) -> qc +#write.table(qc, output, row.names=F, col.names=T, quote=F, sep="\t") +#write.table(qc[selection,], output, row.names=F, col.names=T, quote=F, sep="\t") + +calcTrans <- function(qcRaw, lociFilt = NULL) { + +sel <- rep(T, nrow(qcRaw)) +if (!is.null(lociFilt)) { +paste(qcRaw$X.chr, qcRaw$pos, sep=":") -> qcpos +sel <- ! qcpos %in% lociFilt +} + +qc <- qcRaw[sel,] + +# Calculate transition bias +refA <- grepl("A", qc$ntRef, ignore.case=T) +refC <- grepl("C", qc$ntRef, ignore.case=T) +refG <- grepl("G", qc$ntRef, ignore.case=T) +refT <- grepl("T", qc$ntRef, ignore.case=T) +varA <- grepl("A", qc$ntVar, ignore.case=T) +varC <- grepl("C", qc$ntVar, ignore.case=T) +varG <- grepl("G", qc$ntVar, ignore.case=T) +varT <- grepl("T", qc$ntVar, ignore.case=T) +varN <- grepl(".", qc$ntVar, ignore.case=T) +callA <- grepl("^A", qc$ntVar, ignore.case=T) +callC <- grepl("^C", qc$ntVar, ignore.case=T) +callG <- grepl("^G", qc$ntVar, ignore.case=T) +callT <- grepl("^T", qc$ntVar, ignore.case=T) +ntA <- sum(refA) +ntC <- sum(refC) +ntG <- sum(refG) +ntT <- sum(refT) + +callList <- list(callA, callC, callG, callT) +varList <- list(varA, varC, varG, varT) +refList <- list(refA, refC, refG, refT) + +#tots <- c( +#rep(sum(qc$nRef[refA], qc$nVar[refA]), 4), +#rep(sum(qc$nRef[refC], qc$nVar[refC]), 4), +#rep(sum(qc$nRef[refG], qc$nVar[refG]), 4), +#rep(sum(qc$nRef[refT], qc$nVar[refT]), 4)) + +nvar <- c( +rep(sum(qc$nC[refA], qc$nG[refA], qc$nT[refA]), 4), +rep(sum(qc$nA[refC], qc$nG[refC], qc$nT[refC]), 4), +rep(sum(qc$nA[refG], qc$nC[refG], qc$nT[refG]), 4), +rep(sum(qc$nA[refT], qc$nC[refT], qc$nG[refT]), 4)) + +ncall <- c( +rep(sum(qc$nVar[refA]), 4), +rep(sum(qc$nVar[refC]), 4), +rep(sum(qc$nVar[refG]), 4), +rep(sum(qc$nVar[refT]), 4)) + +nref <- c( +rep(sum(qc$nRef[refA]), 4), +rep(sum(qc$nRef[refC]), 4), +rep(sum(qc$nRef[refG]), 4), +rep(sum(qc$nRef[refT]), 4)) + +tots <- nref + nvar + +nts <- c("A", "C", "G", "T") +sumTrans <- data.frame(trans=paste(rep(nts, each=4), rep(nts, 4), sep=":"), npos=rep(c(ntA, ntC, ntG, ntT), each=4), cnt=rep(0, 16), tot=tots, nvar=nvar, nref=nref, ncall=ncall) + +for (i in 1:4) { + pos <- (i - 1) * 4 +for (j in 1:4) { +# print(sum(refList[[i]] & varList[[j]])) + + cnt <- sum(qc[refList[[i]] & varList[[j]], 8 + j]) + if (i == j) { +# cnt <- sum(qc[refList[[i]] & varN, 8 + j]) + cnt <- NA + } + sumTrans$cnt[pos + j] <- cnt + #print(cnt) +}} + +#sumTrans$cnt / sumTrans$nvar / sumTrans$tot * 1000000 -> tmp +sumTrans$cnt / sumTrans$tot * 1000000 -> tmp + +#totalNT <- sum(qc$nVar) + sum(qc$nRef) +#sumTrans$cnt / median(sumTrans$cnt, na.rm=T) -> sumTrans$cor +sumTrans$cnt / median(sumTrans$cnt, na.rm=T) -> sumTrans$cor +tmp / median(tmp, na.rm=T) -> sumTrans$cor2 + +sumTrans$cor[sumTrans$npos <= 15] <- 1 +sumTrans$cor2[sumTrans$npos <= 15] <- 1 + +#sumTrans$cnt / totalNT -> sumTrans$cor +#sumTrans$cnt / min(sumTrans$cnt, na.rm=T) -> sumTrans$cor + +return(sumTrans) + +} + +calcTransCor <- function(qcRaw, lociFilt = NULL) { + +calcTrans(qcRaw, lociFilt) -> sumTrans + +pCor <- rep(1, nrow(qcRaw)) +paste(qcRaw$ntRef, substr(qcRaw$ntVar, 1, 1), sep=":") -> qcTrans + +for (i in c("A", "C", "G", "T")) { +for (j in c("A", "C", "G", "T")) { + if (i != j) { + tTrans <- paste(i, j, sep=":") + pCor[grepl(tTrans, qcTrans, ignore.case=T)] <- sumTrans$cor2[sumTrans$trans == tTrans] + } + +}} +return(pCor) +} + + +calcTransCorOld <- function(qc) { +# Calculate transition bias +refA <- grepl("A", qc$ntRef, ignore.case=T) +refC <- grepl("C", qc$ntRef, ignore.case=T) +refG <- grepl("G", qc$ntRef, ignore.case=T) +refT <- grepl("T", qc$ntRef, ignore.case=T) +varA <- grepl("A", qc$ntVar, ignore.case=T) +varC <- grepl("C", qc$ntVar, ignore.case=T) +varG <- grepl("G", qc$ntVar, ignore.case=T) +varT <- grepl("T", qc$ntVar, ignore.case=T) +varN <- grepl(".", qc$ntVar, ignore.case=T) +callA <- grepl("^A", qc$ntVar, ignore.case=T) +callC <- grepl("^C", qc$ntVar, ignore.case=T) +callG <- grepl("^G", qc$ntVar, ignore.case=T) +callT <- grepl("^T", qc$ntVar, ignore.case=T) + +callList <- list(callA, callC, callG, callT) +varList <- list(varA, varC, varG, varT) +refList <- list(refA, refC, refG, refT) + +tots <- c( +rep(sum(qc$nRef[refA], qc$nVar[refA]), 4), +rep(sum(qc$nRef[refC], qc$nVar[refC]), 4), +rep(sum(qc$nRef[refG], qc$nVar[refG]), 4), +rep(sum(qc$nRef[refT], qc$nVar[refT]), 4)) + +nvar <- c( +rep(sum(qc$nVar[refA]), 4), +rep(sum(qc$nVar[refC]), 4), +rep(sum(qc$nVar[refG]), 4), +rep(sum(qc$nVar[refT]), 4)) + +nref <- c( +rep(sum(qc$nRef[refA]), 4), +rep(sum(qc$nRef[refC]), 4), +rep(sum(qc$nRef[refG]), 4), +rep(sum(qc$nRef[refT]), 4)) + +nts <- c("A", "C", "G", "T") +sumTrans <- data.frame(trans=paste(rep(nts, each=4), rep(nts, 4), sep=":"), cnt=rep(0, 16), tot=tots, nvar=nvar, nref=nref) + +for (i in 1:4) { + pos <- (i - 1) * 4 +for (j in 1:4) { +# print(sum(refList[[i]] & varList[[j]])) + + cnt <- sum(qc[refList[[i]] & varList[[j]], 8 + j]) + if (i == j) { +# cnt <- sum(qc[refList[[i]] & varN, 8 + j]) + cnt <- NA + } + sumTrans$cnt[pos + j] <- cnt + #print(cnt) +}} +#totalNT <- sum(qc$nVar) + sum(qc$nRef) +sumTrans$cnt / median(sumTrans$cnt, na.rm=T) -> sumTrans$cor +#sumTrans$cnt / totalNT -> sumTrans$cor +#sumTrans$cnt / min(sumTrans$cnt, na.rm=T) -> sumTrans$cor +#print(sumTrans) + +pCor <- rep(1, nrow(qc)) +for (i in 1:4) { + pos <- (i - 1) * 4 +for (j in 1:4) { + if (i != j) { + pCor[refList[[i]] & callList[[j]]] <- sumTrans$cor[pos + j] + } + +}} +return(pCor) +}
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/R/plotsPng.R Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,504 @@ +#!/usr/bin/Rscript + +args <- commandArgs(T) + +print(args[1]) # qc.ann.qual.txt +print(args[2]) # qc2.ann.qtxt +print(args[3]) # qc.targets.txt +print(args[4]) # res.txt (unfiltered) +print(args[5]) # clinvar +print(args[6]) # lociFilt +print(args[7]) # basename +options(warn=1) +print(paste("Reading", args[1], sep=" ")); +read.delim(args[1], header=T, stringsAsFactors=F) -> d +print(paste("Reading", args[2], sep=" ")); +read.delim(args[2], header=T, stringsAsFactors=F) -> d2 +print(paste("Reading", args[3], sep=" ")); +read.delim(args[3], header=T, stringsAsFactors=F) -> qc +print(paste("Reading", args[4], sep=" ")); +read.delim(args[4], header=T, stringsAsFactors=F, row.names=NULL) -> res +print(paste("Reading", args[5], sep=" ")); +## clinvar is a VCF with "##" header lines to skip +headerLineCount <- length( grep('^##', readLines(args[5])) ) +read.delim(args[5], header=T, stringsAsFactors=F, skip=headerLineCount) -> dclin +print(paste("Reading", args[6], sep=" ")); +read.delim(args[6], header=F, stringsAsFactors=F) -> lociFilt +base <- args[7] + +# Error rate per cycle +# VAF distribution +# varDepth distribution ? +# Print coverage plots per amplicon + +tmpCP <- paste(d$X.chr, d$pos, sep=":") +tmpClin <- paste(paste("chr", dclin[,1], sep=""), dclin[,2], sep=":") +tmpSnp <- paste(paste("chr", lociFilt[,1], sep=""), lociFilt[,2], sep=":") + +inClin <- tmpCP %in% tmpClin + +inSnp <- tmpCP %in% tmpSnp + +dir.create(base) +setwd(base) +#unique(unlist(strsplit(d$V3, "\\|"))) -> targets +targets <- qc[,1] +if (1) { + print("Plotting variant heatmap") + # Including off targets increases the amplicon length set at median amplicon length + 10%. + median(qc$end - qc$start) -> maxAmpLn + maxAmpLn <- ceiling(1.2 * maxAmpLn) + print(maxAmpLn) + ampHeatF <- matrix(ncol=maxAmpLn, nrow=nrow(qc)) + ampHeatR <- matrix(ncol=maxAmpLn, nrow=nrow(qc)) + #dPos <- paste(d$chr, d$pos, sep=":") + #errPos <- paste(dclin$chr, dclin$pos, sep=":") + #dPosClin <- dPos %in% errPos + + dPosClin <- !inClin & !inSnp + + for (i in 1:nrow(qc)) { + d$pos %in% qc$start[i]:qc$end[i] -> sel + poss <- d$pos[sel & !dPosClin] - qc$start[i] + 1 + poss <- poss[poss <= maxAmpLn] + ampHeatF[i, poss] <- d$nVar[sel & !dPosClin] + d$nN[sel & !dPosClin] + ampHeatR[i, poss] <- rev(d$nVar[sel & !dPosClin] + d$nN[sel & !dPosClin]) + } + png(paste(base,"heat","png", sep="."), width=960, height=480) + par(mar=c(4,4,4,2) + .1) + + ampHeatF[is.na(ampHeatF)] <- 0 + ampHeatR[is.na(ampHeatR)] <- 0 + layout(matrix(1:2, nrow=2)) + maxN <- quantile(ampHeatF, .99) + #heatmap(ampHeat) + boxplot(ampHeatF, ylim=c(0, maxN), pch=20, cex=.4, main="Non reference counts R1") + rect(150, 0, ncol(ampHeatF), maxN, col="#00000040") + boxplot(ampHeatR, ylim=c(0, maxN), pch=20, cex=.4, main="Non reference counts R2") + rect(150, 0, ncol(ampHeatR), maxN, col="#00000040") + dev.off() + + #d[,7]/d[,4] * 100 -> d$pctREF + #d[,8]/d[,4] * 100 -> d$pctVAR + d$nRef/d$dp * 100 -> d$pctREF + d$nVar/d$dp * 100 -> d$pctVAR + d$vaf <- d$nVar / (d$nVar + d$nRef) * 100 + print("Plotting ref frequencies") + png(paste(base,"raf","png", sep="."), width=480, height=480) + dref <- density(d$pctREF[!dPosClin]) + #plot(dref, ylim=range(dref$y[dref$x < 80] )) + hist(d$pctREF[!dPosClin], breaks=100, ylim=c(0, 30), col="#00000040", border=NA) + dev.off() + + print("Plotting var frequencies") + png(paste(base,"vaf","png", sep="."), width=480, height=480) + dvar <- density(d$pctVAR[!dPosClin]) + #plot(dvar, ylim=range(dvar$y[dvar$x > 20] )) + hist(d$pctVAR[!dPosClin], breaks=100, ylim=c(0, 30), col="#00000040", border=NA) + dev.off() + + # Set vaf cutoff + #q95 <- quantile(d$qScore, .95, na.rm=T) + q95 <- 20 + vs95 <- sd(d$pctVAR[!dPosClin & d$qScore < q95], na.rm=T) + v95 <- mean(d$pctVAR[!dPosClin & d$qScore < q95], na.rm=T) + vs95 * 3 + + nCall <- sum((d$pctVAR > v95) & d$qScore > q95 & !inSnp, na.rm=T) + print(nCall) + print("Plotting vaf vs q") + png(paste(base,"snv-q","png", sep="."), width=480, height=480) + plot(d$qScore, d$pctVAR, pch=20, cex=.5, main=paste("q:", q95, "-", "v:", v95, "--", "s:", nCall, sep=" ")) + abline(h=c(1,5), v=c(20,13), lty=2) + abline(v=q95, h=v95, lty=3, col=2) + points(d$qScore[d$dp < 100], d$pctVAR[d$dp < 100], pch=20, cex=1.2, col=2) + points(d$qScore[d$nVar < 10], d$pctVAR[d$nVar < 10], pch=20, cex=1, col=4) + legend(30,80, c("pass", "dp < 100", "nVar < 10"), col=c(1,2,4), pch=20) + dev.off() + + print("Plotting vaf vs q zoomed") + png(paste(base,"snv-q-zoom","png", sep="."), width=480, height=480) + plot(d$qScore, d$pctVAR, pch=20, cex=.5, xlim=c(0, 40),ylim=c(0,10)) + abline(h=c(1,5), v=c(20,13), lty=2) + abline(v=q95, h=v95, lty=3, col=2) + points(d$qScore[d$dp < 100], d$pctVAR[d$dp < 100], pch=20, cex=1.2, col=2) + points(d$qScore[d$nVar < 10], d$pctVAR[d$nVar < 10], pch=20, cex=1, col=4) + legend("topright", c("pass", "dp < 100", "nVar < 10"), col=c(1,2,4), pch=20) + dev.off() + + print("Plotting ins vs q") + d$vafI <- 0 + d$occI <- 0 + if (sum(d$ins != ".") > 0) { + png(paste(base,"ins-q","png", sep="."), width=480, height=480) + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.character(d$ins[d$ins != "."]), "\\|")), ":")), ncol=2, byrow=T)) -> insDat + colnames(insDat) <- c("seq", "occ") + insDat$seq <- as.character(insDat$seq) + insDat$occ <- as.numeric(as.vector(insDat$occ)) + nchar(insDat$seq) -> insDat$ln + d$occI[d$ins != "."] <- insDat$occ + d$vafI[d$ins != "."] <- insDat$occ / d$nRef[d$ins != "."] + d$qScoreI[d$qScoreI > 1000] <- 1000 + plot(d$qScoreI, d$occI, pch=20, cex=1) + abline(h=c(10), v=c(20,13), lty=2) + # dp 500 + sel <- d$dp < 100 + points(d$qScoreI[sel], d$occI[sel], pch=20, cex=1.2, col=2) + # nVar 10 + #sel <- d$occI < 10 + #points(d$qScoreI[sel], d$occI[sel], pch=20, cex=1, col=3) + # vaf < 0.01 + sel <- d$vafI < 0.01 + points(d$qScoreI[sel], d$occI[sel], pch=20, cex=1, col=4) + legend("topleft", c("pass", "dp < 100", "vaf < 0.01"), col=c(1,2,4), pch=20) + dev.off() + } + + print("Plotting del vs q") + d$vafD <- 0 + d$occD <- 0 + if (sum(d$del != "." ) > 0) { + png(paste(base,"del-q","png", sep="."), width=480, height=480) + data.frame(matrix(unlist(strsplit(unlist(strsplit(as.character(d$del[d$del != "."]), "\\|")), ":")), ncol=2, byrow=T)) -> delDat + colnames(delDat) <- c("seq", "occ") + delDat$seq <- as.character(delDat$seq) + delDat$occ <- as.numeric(as.vector(delDat$occ)) + nchar(delDat$seq) -> delDat$ln + d$occD[d$del != "."] <- delDat$occ + d$vafD[d$del != "."] <- d$occD[d$del != "."] / d$nRef[d$del != "."] + d$qScoreD[d$qScoreD > 1000] <- 1000 + #hist(d$qScoreD, breaks=1000, ylim=c(0,100)) + #print(sum(d$qScoreD > 20)) + #Sys.sleep(1) + plot(d$qScoreD, d$occD, pch=20, cex=1) + abline(h=c(10), v=c(20,13), lty=2) + # dp 500 + sel <- d$dp < 100 + points(d$qScoreD[sel], d$occD[sel], pch=20, cex=1.2, col=2) + # nVar 10 + #sel <- d$occD < 10 + #points(d$qScoreD[sel], d$occD[sel], pch=20, cex=1, col=3) + # vaf < 0.01 + sel <- d$vafD < 0.01 + points(d$qScoreD[sel], d$occD[sel], pch=20, cex=1, col=4) + legend("topleft", c("pass", "dp < 100", "vaf < 0.01"), col=c(1,2,4), pch=20) + dev.off() + } + + sub("chr", "", qc$chr) -> qc$chrn + ampOrd <- order(qc$chrn, qc$start) + + print("Plotting amplicon depths") + png(paste(base,"amp-dp","png", sep="."), width=960, height=480) + barplot(qc$depth[ampOrd]) + abline(h=100, lty=2) + totRead <- sum(qc$depth, na.rm=T) + legend("topright", paste("Total read count: ", totRead, sep="")) + dev.off() +} + +res$POS <- as.numeric(as.vector(res$POS)) +d$pos <- as.numeric(as.vector(d$pos)) + +grepl("a", d$ntRef, ignore.case=T) -> Asel +grepl("c", d$ntRef, ignore.case=T) -> Csel +grepl("g", d$ntRef, ignore.case=T) -> Gsel +grepl("t", d$ntRef, ignore.case=T) -> Tsel +cntr <- 0 + +biasTable <- data.frame(matrix(NA, nrow=length(targets), ncol=12), row.names=targets) +colnames(biasTable) <- c("AC", "AG", "AT", "CA", "CG", "CT", "GA", "GC", "GT", "TA", "TC", "TG") + +for (i in targets) { + sel <- grepl(i, d$amp) + print(i) + for (c in unique(d[sel,1])) { + csel <- d[,1] == c + print(c) + reg <- paste(range(d[sel & csel,2]), collapse="-", sep="-") + creg <- paste(c, reg, sep=":") + + qcsel <- qc[,1] == i + allsel <- sel & csel + clinSel <- dclin$amp == i + clinPos <- dclin$pos[clinSel] +# inClin <- d$pos %in% clinPos + + #dels <- (d[,15] != ".") & allsel + #ins <- (d[,14] != ".") & sel + # print(reg) + # print(creg) + + # Select annotations + # calculate quantiles and plot them +# quantile(d$pctVAR[sel & csel], c(.75,.90,.95,.99), na.rm=T) -> cutoffs + tmp <- d[sel & csel,] + #dels <- tmp[,15] != "." + #ins <- tmp[,14] != "." + dels <- allsel & d$del != "." + ins <- allsel & d$ins != "." + + resTmp <- res[(res$POS >= min(tmp[,2])) & (res$POS <= max(tmp[,2])) & (res$X.CHROM == c),] + #resSel <- res$TARGET == i + png(paste(base, i, "cov", "png", sep="."), width=960, height=480) + + xvec <- c(0, rep(1:(sum(allsel) - 1), each=2), sum(allsel)) + layout(matrix(1:2, ncol=1), heights=c(2,1)) + par(mar=c(0, 4, 4, 7) + .1, xaxt="n") + print("Cov") + plot(NULL, type="n", main=i, xlab="Position", ylab="Depth", xlim=range(d$pos[allsel]), ylim=range(0, d$dp[allsel])) + xvec <- d$pos[allsel] + yvec <- d$dp[allsel] + + polygon(rep(c(xvec, max(xvec) + 1), each=2) - .5, c(0, rep(yvec, each=2), 0), col="#00000010", border=1) + polygon(rep(c(xvec, max(xvec) + 1), each=2) - .5, c(0, rep(rowSums(d[allsel, 7:8]), each=2), 0), col="#00000010") +# polygon(rep(c(xvec, max(xvec) + 1), each=2) - .5, c(0, rep(d$nVar[allsel], each=2), 0), col=2) + varCol <- rep(2, sum(allsel)) + varCol[grepl("^a", d$ntVar[allsel], ignore.case=T)] <- "green" + varCol[grepl("^c", d$ntVar[allsel], ignore.case=T)] <- "blue" + varCol[grepl("^g", d$ntVar[allsel], ignore.case=T)] <- "black" + varCol[grepl("^t", d$ntVar[allsel], ignore.case=T)] <- "red" + rect(xvec-.5,d$nVar[allsel],xvec+.5,0, col=varCol) + + + ampMax <- max(d[allsel,4]) + #abline(v=resTmp$POS, lty=2, col=2) + #delMark <- list() + #insMark <- list() + + for (idx in which(dels)) { + matrix(unlist(strsplit(as.character(as.vector(d[idx,15])), "[:|]")), ncol=2, byrow=T) -> delDat + nchar(delDat[,1]) -> lngts + dpths <- as.numeric(delDat[,2]) + x1 <- d[idx,2] + .5 + x2 <- x1 + lngts - 1 + if (x2 > max(d$pos[allsel])) { + next + } + # delMark[[length(delMark) + 1]] <- c(x1, x2) + rect(x1, ampMax - dpths , x2, ampMax, col="#00000040") + } + + for (idx in which(ins)) { + matrix(unlist(strsplit(as.character(as.vector(d[idx,14])), "[:|]")), ncol=2, byrow=T) -> insDat + nchar(insDat[,1]) -> lngts + dpths <- as.numeric(insDat[,2]) + x1 <- d$pos[idx] + 1 + # insMark[length(insMark) + 1] <- x1 + for (ii in 1:ncol(insDat)) { + polygon( + c(x1, x1 - (.5 * lngts[ii]), x1 + (.5 * lngts[ii])), + c(ampMax, ampMax - dpths[ii], ampMax - dpths[ii]), + , col="#00000040") + } + } + par(xpd=NA) + legend(max(d$pos[allsel]) + sum(allsel) * 0.05, ampMax, legend=c("Filtered nt", "Ref nt", "Non-ref nt"), col=c("#00000040", "#00000080", "red"), pch=15) + legend(max(d$pos[allsel]) + sum(allsel) * 0.05, 0, legend=c("A", "C", "G", "T"), col=c("green", "blue", "black", "red"), pch=15) + par(xpd=F) + par(mar=c(5, 4, 0, 7) + .1, xaxt="s") + plot(NULL, type="n", xlab="Position", ylab=NA, xlim=range(d$pos[allsel]), ylim=c(0,4.5), yaxt="n") + axis(side=2, at=1:4, labels=c("ins", "del", "snv", "ref"), las=2) + abline(h=1:4, col="#00000040") + sres <- nchar(as.character(resTmp$REF)) == nchar(as.character(resTmp$ALT)) + dres <- nchar(resTmp$REF) > nchar(resTmp$ALT) + ires <- nchar(resTmp$REF) < nchar(resTmp$ALT) + + resTmp$marks <- rep(3.4, nrow(resTmp)) + + resTmp$cols <- rep("#00000040", nrow(resTmp)) + resTmp$cols[grepl("^a", resTmp$ALT, ignore.case=T) & sres] <- "green" + resTmp$cols[grepl("^c", resTmp$ALT, ignore.case=T) & sres] <- "blue" + resTmp$cols[grepl("^g", resTmp$ALT, ignore.case=T) & sres] <- "black" + resTmp$cols[grepl("^t", resTmp$ALT, ignore.case=T) & sres] <- "red" + + #resTmp$cols[dres] <- 2 + #resTmp$cols[ires] <- 2 + resTmp$marks[dres] <- 2.4 + resTmp$marks[ires] <- 1.4 + resTmp$markP1 <- resTmp$POS -.5 + resTmp$markP2 <- resTmp$POS +.5 + resTmp$markP1[dres] <- resTmp$POS[dres] +.5 + resTmp$markP2[dres] <- resTmp$POS[dres] +.5 + nchar(resTmp$REF[dres]) - 1 + resTmp$markP1[ires] <- resTmp$POS[ires] +.5 + resTmp$markP2[ires] <- resTmp$POS[ires] +.5 + 1 + ntCol <- rep(1, sum(allsel)) + ntCol[grepl("a", d$ntRef[allsel], ignore.case=T)] <- "green" + ntCol[grepl("c", d$ntRef[allsel], ignore.case=T)] <- "blue" + ntCol[grepl("g", d$ntRef[allsel], ignore.case=T)] <- "black" + ntCol[grepl("t", d$ntRef[allsel], ignore.case=T)] <- "red" + + rect(d$pos[allsel] -.5, 4.4, d$pos[allsel] +.5, 3.6, col=ntCol, border=0) + rect(resTmp$markP1, resTmp$marks, resTmp$markP2, resTmp$marks - .8, col=resTmp$cols, border=0) + + if(length(clinPos != 0)) { + rect(clinPos - .5, 3.5, clinPos + .5, .5, border="black", lwd=2) + } + #lapply(delMark, function(x) { rect(x[1], 2, x[2], 1, col=2, border=NA) }) + #lapply(insMark, function(x) { rect(x[1], 1, x[1] + 1, 0, col=3, border=NA) }) + + # Highlight clinically relevant loci + #for (i in which(dclin$amp == i)) { + # if (dclin$REF[i] == nchar + #} + + dev.off() + + sansClin <- allsel & !inClin + sansSnp <- allsel & !inSnp + + d$nA[sansClin & sansSnp & Asel] -> AA + d$nC[sansClin & sansSnp & Asel] -> AC + d$nG[sansClin & sansSnp & Asel] -> AG + d$nT[sansClin & sansSnp & Asel] -> AT + + d$nA[sansClin & sansSnp & Csel] -> CA + d$nC[sansClin & sansSnp & Csel] -> CC + d$nG[sansClin & sansSnp & Csel] -> CG + d$nT[sansClin & sansSnp & Csel] -> CT + + d$nA[sansClin & sansSnp & Gsel] -> GA + d$nC[sansClin & sansSnp & Gsel] -> GC + d$nG[sansClin & sansSnp & Gsel] -> GG + d$nT[sansClin & sansSnp & Gsel] -> GT + + d$nA[sansClin & sansSnp & Tsel] -> TA + d$nC[sansClin & sansSnp & Tsel] -> TC + d$nG[sansClin & sansSnp & Tsel] -> TG + d$nT[sansClin & sansSnp & Tsel] -> TT + + print("Bias") + png(paste(base, i, "bias", "png", sep="."), width=960, height=480) + + Acnt <- sum(sum(AA), sum(AC), sum(AG), sum(AT)) + Ccnt <- sum(sum(CA), sum(CC), sum(CG), sum(CT)) + Gcnt <- sum(sum(GA), sum(GC), sum(GG), sum(GT)) + Tcnt <- sum(sum(TA), sum(TC), sum(TG), sum(TT)) + + NTsums <- c( + sum(AC)/Acnt, sum(AG)/Acnt, sum(AT)/Acnt, + sum(CA)/Ccnt, sum(CG)/Ccnt, sum(CT)/Ccnt, + sum(GA)/Gcnt, sum(GC)/Gcnt, sum(GT)/Gcnt, + sum(TA)/Tcnt, sum(TC)/Tcnt, sum(TG)/Tcnt) + NTsums[!is.finite(NTsums)] <- 0 + NTsums[is.nan(NTsums)] <- 0 + NTsums[is.na(NTsums)] <- 0 + + barplot(NTsums, names.arg=c("AC", "AG", "AT", "CA", "CG", "CT", "GA", "GC", "GT", "TA", "TC", "TG"), main=i) + dev.off() + biasTable[rownames(biasTable) == i, ] <- NTsums + + print("Cov2") + png(paste(base, i, "cov2", "png", sep="."), width=960, height=480) + layout(matrix(1:2, ncol=1), heights=c(2,1)) + par(mar=c(0, 4, 4, 7) + .1, xaxt="n") + + + dat <- d2[d2$amp == i,] + rled <- rle(sort(dat$pos)) + rds <- sort(unique(dat$X.read)) + lst <- c() + for (ii in order(rled$lengths, decreasing=T)) + { + + rled$values[ii] -> pos + dat$X.read[dat$pos == pos] + lst <- c(lst, rds %in% dat$X.read[dat$pos == pos]) + + } + #xlim <- range(dat$pos) + xlim=range(d$pos[allsel]) + ylim=range(0, d$dp[allsel]) + plot(NULL, xlim=xlim, ylim=ylim, main=i, ylab="Depth") + rect(xlim[1] - 0.5, 0, xlim[2] + .5, ylim[2], col="#00000010") + if (length(lst) > 0) { + matrix(lst, nrow=length(rds), byrow=F) -> mat + do.call( order, data.frame(mat) ) -> ord + for (e in 1:length(ord)) { + sel <- dat$X.read == rds[ord[e]] + colvec <- rep(1, sum(sel)) + colvec[grepl("A$", dat$event[sel], ignore.case=T)] <- "green" + colvec[grepl("C$", dat$event[sel], ignore.case=T)] <- "blue" + colvec[grepl("G$", dat$event[sel], ignore.case=T)] <- "black" + colvec[grepl("T$", dat$event[sel], ignore.case=T)] <- "red" + #points(dat$pos[ sel ], rep(e, sum(sel)), col=colvec, pch=20, cex=.2) + segments(dat$pos[ sel ] - .5, rep(e, sum(sel)), dat$pos[ sel ] + .5, rep(e, sum(sel)), col=colvec, pch=20, cex=.2) + } + } + + par(xpd=NA) + legend(max(d$pos[allsel]) + sum(allsel) * 0.05, ampMax, legend=c("Filtered nt", "Ref nt", "Non-ref nt"), col=c("#00000040", "#00000080", "red"), pch=15) + legend(max(d$pos[allsel]) + sum(allsel) * 0.05, 0, legend=c("A", "C", "G", "T"), col=c("green", "blue", "black", "red"), pch=15) + par(xpd=F) + par(mar=c(5, 4, 0, 7) + .1, xaxt="s") + plot(NULL, type="n", xlab="Position", ylab=NA, xlim=range(d$pos[allsel]), ylim=c(0,4.5), yaxt="n") + axis(side=2, at=1:4, labels=c("ins", "del", "snv", "ref"), las=2) + abline(h=1:4, col="#00000040") + sres <- nchar(as.character(resTmp$REF)) == nchar(as.character(resTmp$ALT)) + dres <- nchar(resTmp$REF) > nchar(resTmp$ALT) + ires <- nchar(resTmp$REF) < nchar(resTmp$ALT) + + resTmp$marks <- rep(3.4, nrow(resTmp)) + + resTmp$cols <- rep("#00000040", nrow(resTmp)) + resTmp$cols[grepl("^a", resTmp$ALT, ignore.case=T) & sres] <- "green" + resTmp$cols[grepl("^c", resTmp$ALT, ignore.case=T) & sres] <- "blue" + resTmp$cols[grepl("^g", resTmp$ALT, ignore.case=T) & sres] <- "black" + resTmp$cols[grepl("^t", resTmp$ALT, ignore.case=T) & sres] <- "red" + + #resTmp$cols[dres] <- 2 + #resTmp$cols[ires] <- 2 + resTmp$marks[dres] <- 2.4 + resTmp$marks[ires] <- 1.4 + resTmp$markP1 <- resTmp$POS -.5 + resTmp$markP2 <- resTmp$POS +.5 + resTmp$markP1[dres] <- resTmp$POS[dres] +.5 + resTmp$markP2[dres] <- resTmp$POS[dres] +.5 + nchar(resTmp$REF[dres]) - 1 + resTmp$markP1[ires] <- resTmp$POS[ires] +.5 + resTmp$markP2[ires] <- resTmp$POS[ires] +.5 + 1 + ntCol <- rep(1, sum(allsel)) + ntCol[grepl("a", d$ntRef[allsel], ignore.case=T)] <- "green" + ntCol[grepl("c", d$ntRef[allsel], ignore.case=T)] <- "blue" + ntCol[grepl("g", d$ntRef[allsel], ignore.case=T)] <- "black" + ntCol[grepl("t", d$ntRef[allsel], ignore.case=T)] <- "red" + + rect(d$pos[allsel] -.5, 4.4, d$pos[allsel] +.5, 3.6, col=ntCol, border=0) + rect(resTmp$markP1, resTmp$marks, resTmp$markP2, resTmp$marks - .8, col=resTmp$cols, border=0) + + if(length(clinPos != 0)) { + rect(clinPos - .5, 3.5, clinPos + .5, .5, border="black", lwd=2) + } + + + dev.off() + +# png(paste(base, i, "vaf", "png", sep="."), width=960, height=480) +# plot(d[sel & csel,2], d$vaf[sel & csel], type="l", ylim=c(0,100), main=paste(i, creg, cutoffs[3], sep=" "), xlab="position", ylab="%", col=2) + #lines(d[sel & csel,2], d$pctVAR[sel & csel], type="l", col=2) +# abline(h=100) +# abline(h=c(1,5,10,50,90,95,99), lty=3, col=1) +# abline(h=cutoffs[3], lty=4, col=2) +# abline(v=c(limP[1], limP[1] + 150, limP[2] - 150, limP[2]),lty=4) +# abline(v=c(qc[qcsel,8:9]), lty=5, col=2) +# if (length(labs != 0)) { +# text(resTmp$POS[resTmp$vaf > (cutoffs[3]/100)], 50, labels=resTmp$Amino_Acid_change[resTmp$vaf > (cutoffs[3]/100)]) +# abline(v=resTmp$POS[resTmp$vaf > (cutoffs[3]/100)], col="grey", lty=4) +# } +# dev.off() + } +} + +png(paste(base, "biasheat", "png", sep="."), width=960, height=960) +write.table(biasTable, paste(base, "bias", "tsv", sep="."), sep="\t") +biasTable[is.na(biasTable)] <- 0 +heatmap(data.matrix(biasTable), Colv=NA, scale="r") +dev.off() +png(paste(base, "bias", "png", sep="."), width=960, height=480) +boxplot(data.matrix(biasTable), pch=20, cex=.5) +dev.off() +warnings() +#hist(d$pctVAR[d$pctVAR < 20], breaks=40, ylim=c(0,1000)) +#hist(d$pctREF[d$pctREF > 80], breaks=40, ylim=c(0,1000)) + +#print(summary(d$pctVAR)) + +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/filter.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,133 @@ +#!/usr/bin/perl -w + +use strict; + +my $file = shift; +my $canonicals = shift; +my $clinvar = shift; +my $cosmic = shift; +my $cosmicNC = shift; + +my $minDP = 100; +my $minVAR = 10; +my $minVAF = 0.01; + +my %can = (); +my %nm = (); +my %cvHsh = (); + +print STDERR "Reading in canonicals,..."; +open CAN, "<$canonicals"; +while (<CAN>) { + chomp; + my @row = split(/\t/, $_); + $can{$row[0]} = @row[1 .. $#row]; + my $pri = 0; + $nm{$_} = $pri++ foreach @row[1 .. $#row]; +} +close CAN; + +print STDERR "Reading clinvars...\n"; +open CV, "<$clinvar"; +while (<CV>) { last if (/#CHROM/); } +while (<CV>) { + chomp; + my @row = split(/\t/, $_); + push @{$cvHsh{"chr".$row[0].":".$row[1]}}, [@row]; +} +close CV; + +print STDERR "Reading COSMIC...\n"; +open CV, "<$cosmic"; +while (<CV>) { last if (/#CHROM/); } +while (<CV>) { + chomp; + my @row = split(/\t/, $_); + push @{$cvHsh{"chr".$row[0].":".$row[1]}}, [@row]; +} +close CV; + +print STDERR "Reading COSMICNC...\n"; +open CV, "<$cosmicNC"; +while (<CV>) { last if (/#CHROM/); } +while (<CV>) { + chomp; + my @row = split(/\t/, $_); + push @{$cvHsh{"chr".$row[0].":".$row[1]}}, [@row]; +} + +close CV; +print STDERR "done!\n"; + +print STDERR "Processing $file\n"; + +open F, "<$file"; +my $head = readline(F); +chomp $head; + +print $head . "\tvaf\n"; + +my @rowHead = split(/\t/, $head); +my $colN = 0; +my %col = map { + $_ => $colN++ } @rowHead; + +while (<F>) { + chomp; + my $line = $_; + my @row = split(/\t/, $_); + next unless (exists($can{$row[$col{Gene_Name}]})); + my $trans = $row[$col{Transcript_ID}]; + $trans =~ s/\..*$//; + + ## impossible to switch off these two transcript filters + ## so commented out + # if (not exists($nm{$trans})) { + # print STDERR "Unknown transcript: $row[$col{Gene_Name}] $trans\n"; + # next; + # } + # elsif ($nm{$trans} != 0) { + # print STDERR "Non cannonical: $row[$col{Gene_Name}] $trans\n"; + # next; + # } + + # Annotate clinincal variants and cosmic mutations + + my $chr = $row[$col{"#CHROM"}]; + my $pos = $row[$col{POS}]; + + if (exists($cvHsh{"$chr:$pos"})) { + my $rows = $cvHsh{"$chr:$pos"}; + my $cv = join("|", map { $_->[2] } @$rows); + $row[2] .= "|$cv"; + } + + # Filter INTERGENIC + next if ($row[$col{Context}] eq "INTERGENIC"); + + # Filter SYNONYMOUS_CODING + # Dubbel mutatie BRAF +# next if ($row[$col{Context}] eq "SYNONYMOUS_CODING"); + + # Filter INTRON + next if ($row[$col{Context}] eq "INTRON"); + + # Filter dbSNP +# next if ($row[2] ne "."); + + # Filter depth + next if ($row[$col{DP}] < $minDP); + + my ($nref, $nvar) = split(/,/, $row[$col{AD}]); + # Filter var depth +# print STDERR "DEBUG: " . $nvar . "\n"; sleep 1; + next if ($nvar < $minVAR); + + my $vaf = $nvar / ($nref + $nvar); +# print STDERR "DEBUG: " . $vaf . "\n"; + # Filter vaf + next if ($vaf < $minVAF); + + print join("\t", @row, $vaf) . "\n"; +} +close F;
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/mkHtmlReport.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,234 @@ +#!/usr/bin/perl -w + +use strict; +use Cwd; +use Spreadsheet::WriteExcel; + +$| = 1; +my $dir = shift || "./"; +my $outdir = shift || "./"; +my $pat = shift || ""; +my $cwd = cwd(); +(my $runName = $cwd) =~ s/^.*\/(.*?)$/$1/; + +# QC +# Results +my @samples = (); +#open INDEX, ">$outdir/index.html"; +my $htmlHead = qq( +<!DOCTYPE html> +<html> +<head> +<style type="text/css"> +body {font-family:arial;} +table {font-family:arial;border-collapse: collapse; font-size: smaller;} +th {border: 1px solid gray; padding: 5px;} +td {border: 1px solid gray; padding: 5px; text-align: right;} +</style> +</head> +<body> +); +#print INDEX $htmlHead; +opendir DIR, "$dir"; +while (my $cd = readdir DIR) { + if ($cd =~ /(.*$pat)\.qc\.targets\.txt$/) { + my $sam = $1; +# next if ($sam =~ /R[12]/); + print STDERR $1 . "\n"; + push @samples, $1; + } +} +close DIR; + +#print INDEX "<table>"; +#print INDEX "<tr><th>Download:</th><th><a href=\"runQC.xls\">runQC.xls</a></th>"; +#print INDEX "<tr><th>Sample</th><th>BAM</th><th>snp</th><th>indel</th><th>readCnt</th><th>Amp > 100</th>\n"; +#foreach my $sam (sort @samples) { +# print INDEX "<tr><td><a href=$sam.html>$sam</a></td><td><a href=$sam.bam>BAM</a></td><td><a href=$sam.bam.bai>BAI</a></td></tr>\n"; + +#} +my %link = (); +my $excelBook0 = Spreadsheet::WriteExcel->new("$outdir/runQC.xls"); +my $excel0 = $excelBook0->add_worksheet("table1"); +my $excel0Ref = [[qw/sampleName runName totalReads pct100 ntbGenes/]]; + + +foreach my $sample (sort @samples) { + print STDERR "Processing $sample\n"; +# next if ($sample =~ /R[12]/); + + my $readCnt = 0; + my $amp100 = 0; + my %ntbGenes = (); + + open OUT, ">$outdir/$sample.html"; + open OUT2, ">$outdir/$sample.tsv"; + my $excelBook = Spreadsheet::WriteExcel->new("$outdir/$sample.xls"); + my $excel1 = $excelBook->add_worksheet("table1"); + my $excel2 = $excelBook->add_worksheet("table2"); + print OUT $htmlHead; + my %QC = (); + open QC, "<$dir/$sample.qc.targets.txt"; + readline QC; + print STDERR "Reading in $sample.qc.targets.txt\n"; + while (<QC>) { + chomp; + my @row = split(/\t/, $_); + my @id = split(/[\_\.\-:]/, $row[0]); + $row[-1] = 0 if ($row[-1] eq "NA"); + $readCnt += $row[-1]; # DP + if ($#id != 10) { + $id[0] =~ /(\D+)(\d+)/; + $id[0] = $2; + unshift @id, $1; + } + + if ($row[-1] >= 100) { + $amp100++ + } + else { + $ntbGenes{$row[0]}{dp} = $row[-1]; + $ntbGenes{$row[0]}{id} = [@id]; + } + + $QC{$row[0]}{QC} = [@id, @row];# if ($id[0]); + foreach my $c ($row[4] .. $row[5]) { + $link{$id[-3] . ":" . $c}{$row[0]} = "Assay"; + } + foreach my $c ($row[2] .. $row[4], $row[5] .. $row[3]) { + $link{$id[-3] . ":" . $c}{$row[0]} = "LSO"; + } + } + close QC; + + open RES, "<$dir/$sample.res.filtered.tsv" or die "Unable to open $dir/$sample\n"; + my %uniq = (); + my $colCnt = 0; + my $resHead = readline(RES); + chomp $resHead; + $resHead =~ s/^#//; + $resHead =~ s/\s+$//; + my %resCol = map { $_ => $colCnt++ } split(/\t/, $resHead); + my @keyColsN = qw/QUAL Gene_Name Codon_Change Amino_Acid_change vaf DP AD Tag CHROM POS ID REF ALT Context Effect_Impact Functional_Class Amino_Acid_length Gene_Coding Transcript_ID Exon_Rank/; +# my @keyColsN = qw/CHROM POS ID REF ALT QUAL DP AD vaf Context Effect_Impact Functional_Class Codon_Change Amino_Acid_change Amino_Acid_length Gene_Name Coding Transcript Exon Tag/; + my @keyColsI = map { $resCol{$_} } @keyColsN; + foreach my $i (0 .. $#keyColsN) { + print STDERR join(":", $i, $keyColsN[$i], $keyColsI[$i]) . "\n"; + } + + print STDERR "Processing results\n"; + while (<RES>) { + chomp; + my @row = split(/\t/, $_); + my $cpos = join(":", @row[0, 1]); + if (exists $link{$cpos}) { +# my $key = join(":", @row[0 .. 4,6, 9,10,11,12,14 .. 21]); + my $key = join(":", @row[@keyColsI]); + #print STDERR join(":", @keyColsI) . "\n"; +# print STDERR join(":", @row) . "\n"; sleep 1; + if (not exists($uniq{$key})) { + foreach my $locus (keys(%{$link{$cpos}})) { + next if ($link{$cpos}{$locus} eq "LSO"); + push @{$QC{$locus}{RES}}, [@row, $link{$cpos}{$locus}]; + # print STDERR "Adding $key to $locus\n\n"; #sleep 1; + } + $uniq{$key} = 0; + } + else { + # print STDERR $key . " : Exists\n\n"; #sleep 1; + } + } + } + close RES; + + ## Rplots that are not self-explanatory enough + #print OUT "<img src=\"$sample/$sample.vaf.png\">"; + #print OUT "<img src=\"$sample/$sample.raf.png\">"; + #print OUT "<img src=\"$sample/$sample.snv-q.png\">"; + #print OUT "<img src=\"$sample/$sample.snv-q-zoom.png\">"; + #print OUT "<img src=\"$sample/$sample.ins-q.png\">"; + #print OUT "<img src=\"$sample/$sample.del-q.png\">"; + + print OUT "<img src=\"$sample/$sample.amp-dp.png\">"; + #print OUT "<img src=\"$sample/$sample.heat.png\">"; + #print OUT "<img src=\"$sample/$sample.bias.png\">"; + #print OUT "<img src=\"$sample/$sample.biasheat.png\">"; + #print OUT "<img src=\"$sample/$sample.vafcut.png\">"; + print OUT "<table border=1><tr><th>Download:</th><th><a href=\"$sample.tsv\">TSV</a></th>"; + print OUT "<th><a href=\"$sample.xls\">XLS</a></th></table>"; + print OUT "<table border=1>\n"; +# my @colnames = qw/depth chr pos id ref var qual DP AD vaf context impact effectClass codonChange AAChange RefSeqLength geneName RefSeqClass RefSeqID Exon Tag/; + my @colnames = ("depth", @keyColsN); + print OUT "<tr>" . join("", map { "<th>$_</th>" } ("Amplicon", "c","c2", "b", @colnames)) . "</tr>"; + print OUT2 join("\t", "Amplicon", @colnames) . "\n"; + my $excelAref = [["Amplicon", @colnames]]; + my $excelAref2 = [[qw/gene exon protein vaf func depth /]]; + my %rescnt = (); + foreach my $locus (sort keys(%QC)) { + # my @targets = keys(%{$QC{$locus}{QC}}); +# print OUT "</td>"; + my $nres = 1; + $nres = scalar(@{$QC{$locus}{RES}}) if ($QC{$locus}{RES}); + + print OUT "<tr><td rowspan=\"$nres\">$locus</td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.cov.png\">c</a></td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.cov2.png\">c2</a></td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.bias.png\">b</a></td>\n"; + print OUT "<td rowspan=\"$nres\">$QC{$locus}{QC}->[-1]</td>\n"; #<td rowspan=\"$nres\">"; + + foreach my $res (@{$QC{$locus}{RES}}) { + $res = [map {$_ || ""} @$res]; + print OUT "<td>\n"; + print OUT join("</td><td>\n", @{$res}[@keyColsI]); + print OUT "</td></tr><tr>\n"; + print OUT2 join("\t", $locus, $QC{$locus}{QC}->[-1], @{$res}[@keyColsI]) . "\n"; + push @$excelAref, [$locus, $QC{$locus}{QC}->[-1], @{$res}[@keyColsI]]; + + # qw/QUAL Gene_Name Codon_Change Amino_Acid_change vaf DP AD Tag CHROM POS ID REF ALT Context Effect_Impact Functional_Class Amino_Acid_length Coding Transcript Exon/; + push @$excelAref2, [map {$_ || "NA"} @{$res}[map { $resCol{$_} } (qw/Gene_Name Exon_Rank Amino_Acid_change vaf Functional_Class/)], $QC{$locus}{QC}->[-1]]; +# push @$excelAref2, [map {$_ || "NA"} @{$res}[[qw/Gene_Name Exon_Rank Cdna_change Amino_Acid_change vaf Functional_Class/]], $QC{$locus}{QC}->[-1]]; + my $pl = $res->[$keyColsI[7]]; + my $ref = $res->[$keyColsI[11]]; + my $var = $res->[$keyColsI[12]]; +# print STDERR "$pl $ref $var\n"; sleep 1; + if (length($ref) == length($var)) { + $rescnt{$pl . "snp"}++; + } + else { + $rescnt{$pl . "indel"}++; + } +# $rescnt++; + } + print STDERR $locus . ":" . $nres . "\n"; + print STDERR $locus . ":" . join("-", @{$QC{$locus}{RES}}) . "\n"; + if (scalar(@{$QC{$locus}{RES}}) == 0) { #$nres == 0) { + print OUT2 join("\t", $locus, $QC{$locus}{QC}->[-1], ("-") x scalar(@keyColsI)) . "\n"; + push @$excelAref, [$locus, $QC{$locus}{QC}->[-1], ("-") x scalar(@keyColsI)]; + } + print OUT "</tr>\n"; + } + print OUT "</table>\n"; + print OUT "</body></html>\n"; + close OUT; + close OUT2; + $excel1->write_col(0,0, $excelAref); + $excel2->write_col(0,0, $excelAref2); + $excelBook->close(); + my @resCnt = map { $rescnt{$_} || 0 } qw/Falcosnp Falcoindel/; + my $pctGood = sprintf("%.2f", $amp100 / scalar(keys(%QC)) * 100); + #print INDEX "<tr><td><a href=$sample.html>$sample</a></td><td><a href=$sample.bam>BAM</a></td><td>$resCnt[0]</td><td>$resCnt[1]</td><td>$readCnt</td><td>$pctGood</td></tr>\n"; + my $ntbsAmps = join(",", map { s/^(.*?)\.chr.*$/$1/; $_; } keys(%ntbGenes)); + push @{$excel0Ref}, [$sample, $runName, $readCnt, $pctGood, $ntbsAmps]; +} + +$excel0->write_col(0,0, $excel0Ref); +$excelBook0->close(); + +#print INDEX "</table>"; +#print INDEX "<img src=\"alnStats.png\">"; +#print INDEX "<img src=\"errStats.png\">"; +#print INDEX "<img src=\"qualStats.png\">"; +#print INDEX "</html>"; +#close INDEX; + +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/mkHtmlReportGalaxy.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,206 @@ +#!/usr/bin/perl -w + +use strict; +use Cwd; +use Spreadsheet::WriteExcel; + +$| = 1; +my $sample = shift || die "Missing input\n"; +my $qc_targets_txt = shift || die "Missing input\n"; +my $dir = shift || "./"; +my $outdir = shift || "./"; +my $pat = shift || ""; +my $cwd = cwd(); +(my $runName = $cwd) =~ s/^.*\/(.*?)$/$1/; + +# QC +# Results +my @samples = (); +my $htmlHead = qq( +<!DOCTYPE html> +<html> +<head> +<style type="text/css"> +body {font-family:arial;} +table {font-family:arial;border-collapse: collapse; font-size: smaller;} +th {border: 1px solid gray; padding: 5px;} +td {border: 1px solid gray; padding: 5px; text-align: right;} +</style> +</head> +<body> +); + +my %link = (); +my $excelBook0 = Spreadsheet::WriteExcel->new("$outdir/runQC.xls"); +my $excel0 = $excelBook0->add_worksheet("table1"); +my $excel0Ref = [[qw/sampleName runName totalReads pct100 ntbGenes/]]; + +print STDERR "Processing $sample\n"; +# next if ($sample =~ /R[12]/); + +my $readCnt = 0; +my $amp100 = 0; +my %ntbGenes = (); + +open OUT, ">$outdir/$sample.html"; +open OUT2, ">$outdir/$sample.tsv"; +my $excelBook = Spreadsheet::WriteExcel->new("$outdir/$sample.xls"); +my $excel1 = $excelBook->add_worksheet("table1"); +my $excel2 = $excelBook->add_worksheet("table2"); +print OUT $htmlHead; +my %QC = (); +open QC, "<$qc_targets_txt" or die "Unable to open qc_targets_txt\n"; +readline QC; +print STDERR "Reading in $qc_targets_txt\n"; +while (<QC>) { + chomp; + my @row = split(/\t/, $_); + my @id = split(/[\_\.\-:]/, $row[0]); + $row[-1] = 0 if ($row[-1] eq "NA"); + $readCnt += $row[-1]; # DP + if ($#id != 10) { + $id[0] =~ /(\D+)(\d+)/; + $id[0] = $2; + unshift @id, $1; + } + + if ($row[-1] >= 100) { + $amp100++ + } + else { + $ntbGenes{$row[0]}{dp} = $row[-1]; + $ntbGenes{$row[0]}{id} = [@id]; + } + + $QC{$row[0]}{QC} = [@id, @row];# if ($id[0]); + foreach my $c ($row[4] .. $row[5]) { + $link{$id[-3] . ":" . $c}{$row[0]} = "Assay"; + } + foreach my $c ($row[2] .. $row[4], $row[5] .. $row[3]) { + $link{$id[-3] . ":" . $c}{$row[0]} = "LSO"; + } +} +close QC; + +open RES, "<$dir/$sample.res.filtered.tsv" or die "Unable to open $dir/$sample\n"; +my %uniq = (); +my $colCnt = 0; +my $resHead = readline(RES); +chomp $resHead; +$resHead =~ s/^#//; +$resHead =~ s/\s+$//; +my %resCol = map { $_ => $colCnt++ } split(/\t/, $resHead); +my @keyColsN = qw/QUAL Gene_Name Codon_Change Amino_Acid_change vaf DP AD Tag CHROM POS ID REF ALT Context Effect_Impact Functional_Class Amino_Acid_length Gene_Coding Transcript_ID Exon_Rank/; +# my @keyColsN = qw/CHROM POS ID REF ALT QUAL DP AD vaf Context Effect_Impact Functional_Class Codon_Change Amino_Acid_change Amino_Acid_length Gene_Name Coding Transcript Exon Tag/; +my @keyColsI = map { $resCol{$_} } @keyColsN; +foreach my $i (0 .. $#keyColsN) { + print STDERR join(":", $i, $keyColsN[$i], $keyColsI[$i]) . "\n"; +} + +print STDERR "Processing results\n"; +while (<RES>) { + chomp; + my @row = split(/\t/, $_); + my $cpos = join(":", @row[0, 1]); + if (exists $link{$cpos}) { +# my $key = join(":", @row[0 .. 4,6, 9,10,11,12,14 .. 21]); + my $key = join(":", @row[@keyColsI]); + #print STDERR join(":", @keyColsI) . "\n"; +# print STDERR join(":", @row) . "\n"; sleep 1; + if (not exists($uniq{$key})) { + foreach my $locus (keys(%{$link{$cpos}})) { + next if ($link{$cpos}{$locus} eq "LSO"); + push @{$QC{$locus}{RES}}, [@row, $link{$cpos}{$locus}]; + # print STDERR "Adding $key to $locus\n\n"; #sleep 1; + } + $uniq{$key} = 0; + } + else { + # print STDERR $key . " : Exists\n\n"; #sleep 1; + } + } +} +close RES; + +## Rplots that are not self-explanatory enough +#print OUT "<img src=\"$sample/$sample.vaf.png\">"; +#print OUT "<img src=\"$sample/$sample.raf.png\">"; +#print OUT "<img src=\"$sample/$sample.snv-q.png\">"; +#print OUT "<img src=\"$sample/$sample.snv-q-zoom.png\">"; +#print OUT "<img src=\"$sample/$sample.ins-q.png\">"; +#print OUT "<img src=\"$sample/$sample.del-q.png\">"; + +print OUT "<img src=\"$sample/$sample.amp-dp.png\">"; +#print OUT "<img src=\"$sample/$sample.heat.png\">"; +#print OUT "<img src=\"$sample/$sample.bias.png\">"; +#print OUT "<img src=\"$sample/$sample.biasheat.png\">"; +#print OUT "<img src=\"$sample/$sample.vafcut.png\">"; +print OUT "<table border=1><tr><th>Download:</th><th><a href=\"$sample.tsv\">TSV</a></th>"; +print OUT "<th><a href=\"$sample.xls\">XLS</a></th></table>"; +print OUT "<table border=1>\n"; +# my @colnames = qw/depth chr pos id ref var qual DP AD vaf context impact effectClass codonChange AAChange RefSeqLength geneName RefSeqClass RefSeqID Exon Tag/; +my @colnames = ("depth", @keyColsN); +print OUT "<tr>" . join("", map { "<th>$_</th>" } ("Amplicon", "c","c2", "b", @colnames)) . "</tr>"; +print OUT2 join("\t", "Amplicon", @colnames) . "\n"; +my $excelAref = [["Amplicon", @colnames]]; +my $excelAref2 = [[qw/gene exon protein vaf func depth /]]; +my %rescnt = (); +foreach my $locus (sort keys(%QC)) { +# my @targets = keys(%{$QC{$locus}{QC}}); +# print OUT "</td>"; + my $nres = 1; + $nres = scalar(@{$QC{$locus}{RES}}) if ($QC{$locus}{RES}); + + print OUT "<tr><td rowspan=\"$nres\">$locus</td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.cov.png\">c</a></td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.cov2.png\">c2</a></td>\n"; + print OUT "<td rowspan=\"$nres\"><a href=\"$sample/$sample.$locus.bias.png\">b</a></td>\n"; + print OUT "<td rowspan=\"$nres\">$QC{$locus}{QC}->[-1]</td>\n"; #<td rowspan=\"$nres\">"; + + foreach my $res (@{$QC{$locus}{RES}}) { + $res = [map {$_ || ""} @$res]; + print OUT "<td>\n"; + print OUT join("</td><td>\n", @{$res}[@keyColsI]); + print OUT "</td></tr><tr>\n"; + print OUT2 join("\t", $locus, $QC{$locus}{QC}->[-1], @{$res}[@keyColsI]) . "\n"; + push @$excelAref, [$locus, $QC{$locus}{QC}->[-1], @{$res}[@keyColsI]]; + +# qw/QUAL Gene_Name Codon_Change Amino_Acid_change vaf DP AD Tag CHROM POS ID REF ALT Context Effect_Impact Functional_Class Amino_Acid_length Coding Transcript Exon/; + push @$excelAref2, [map {$_ || "NA"} @{$res}[map { $resCol{$_} } (qw/Gene_Name Exon_Rank Amino_Acid_change vaf Functional_Class/)], $QC{$locus}{QC}->[-1]]; +# push @$excelAref2, [map {$_ || "NA"} @{$res}[[qw/Gene_Name Exon_Rank Cdna_change Amino_Acid_change vaf Functional_Class/]], $QC{$locus}{QC}->[-1]]; + my $pl = $res->[$keyColsI[7]]; + my $ref = $res->[$keyColsI[11]]; + my $var = $res->[$keyColsI[12]]; +# print STDERR "$pl $ref $var\n"; sleep 1; + if (length($ref) == length($var)) { + $rescnt{$pl . "snp"}++; + } + else { + $rescnt{$pl . "indel"}++; + } +# $rescnt++; + } + print STDERR $locus . ":" . $nres . "\n"; + print STDERR $locus . ":" . join("-", @{$QC{$locus}{RES}}) . "\n"; + if (scalar(@{$QC{$locus}{RES}}) == 0) { #$nres == 0) { + print OUT2 join("\t", $locus, $QC{$locus}{QC}->[-1], ("-") x scalar(@keyColsI)) . "\n"; + push @$excelAref, [$locus, $QC{$locus}{QC}->[-1], ("-") x scalar(@keyColsI)]; + } + print OUT "</tr>\n"; +} +print OUT "</table>\n"; +print OUT "</body></html>\n"; +close OUT; +close OUT2; +$excel1->write_col(0,0, $excelAref); +$excel2->write_col(0,0, $excelAref2); +$excelBook->close(); +my @resCnt = map { $rescnt{$_} || 0 } qw/Falcosnp Falcoindel/; +my $pctGood = sprintf("%.2f", $amp100 / scalar(keys(%QC)) * 100); +my $ntbsAmps = join(",", map { s/^(.*?)\.chr.*$/$1/; $_; } keys(%ntbGenes)); +push @{$excel0Ref}, [$sample, $runName, $readCnt, $pctGood, $ntbsAmps]; + +$excel0->write_col(0,0, $excel0Ref); +$excelBook0->close(); + +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/perAmpliconAnalysis.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,314 @@ +#!/usr/bin/perl -w + +use strict; + +my $bam = shift; +my $ref = shift; +my $manifest = shift; +my $base = shift || "output"; +my $samtools = shift || `which samtools`; +my $fai = $ref . ".fai"; +my $Qthreshold = 30; +my $QavgLim = 0; + +open FAI, "<$fai"; +my %idx = (); +print STDOUT "Reading fa index ... "; +while (<FAI>) { + chomp; + my @row = split(/\t/, $_); + $idx{$row[0]} = [@row]; +} +print STDOUT "done\n"; + +close FAI; +open REF, "<$ref"; + +my %stats = (); +my %manif = (); +my %targets = (); +my %probe = (); +my %hash = (); + +open M, "<$manifest"; +while (<M>) { last if (/\[Probes\]/) } +readline(M); +while (<M>) { + chomp; + if (/\[Targets\]/) { + my $h = readline M; + chomp $h; + my @H = split(/\t/, $h); + last; + } + my @row = split(/\t/, $_); + $probe{$row[2]}{probe} = [@row]; + $probe{$row[2]}{ULSO} = $row[9]; + $probe{$row[2]}{DLSO} = $row[11]; +} + +while (<M>) { + chomp; + s/\s+$//; + my @row = split(/\t/, $_); + push @{$targets{$row[3]}{$_}}, $row[0] foreach ($row[4] .. $row[5]); + my $aTarget = $row[0] . "-" . $row[3] . ":". "$row[4]-$row[5]"; + if (not exists($stats{$aTarget}{target})) { + $stats{$aTarget}{target} = [@row]; + $stats{$aTarget}{ln} = $row[5] - $row[4] + 1; + $stats{$aTarget}{n} = 0; + $stats{$aTarget}{sam} = []; + $stats{$aTarget}{depth} = 0; + $stats{$aTarget}{covs} = []; + $stats{$aTarget}{chr} = $row[3]; + $stats{$aTarget}{start} = $row[4]; + $stats{$aTarget}{end} = $row[5]; + $stats{$aTarget}{ULSO} = $probe{$row[0]}{ULSO}; + $stats{$aTarget}{DLSO} = $probe{$row[0]}{DLSO}; + $stats{$aTarget}{assayStart} = $row[4] + length($probe{$row[0]}{ULSO}); + $stats{$aTarget}{assayEnd} = $row[5] - length($probe{$row[0]}{DLSO}); + } + foreach my $i (0 .. 5) { + foreach my $j (0 .. 5) { + $hash{$row[3]}{$row[4] + $i}{$row[5] - $row[4] + $j} = $aTarget; + $hash{$row[3]}{$row[4] + $i}{$row[5] - $row[4] - $j} = $aTarget; + $hash{$row[3]}{$row[4] - $i}{$row[5] - $row[4] + $j} = $aTarget; + $hash{$row[3]}{$row[4] - $i}{$row[5] - $row[4] - $j} = $aTarget; + } + } +} +close M; + +# Open output +open QC, ">$base.qc.ann.txt"; +open QC2, ">$base.qc2.ann.txt"; +open TARGET, ">$base.qc.targets.txt"; + +# Stampy check +my $stampy = 0; +open SAMH, "$samtools view -H $bam |"; +while (<SAMH>) { + $stampy = 1 if (/PN:stampy/); + if (/PN:stampy/) { + print STDERR "[WARNING]: Stampy aligned reads is no longer supported.\n"; + } + if (/SO:unsorted/) { + print STDERR "[Warning]: Alignments seem to be unsorted.\n"; + } +} +close SAMH; + +open SAM, "$samtools view -F 4 $bam |"; +while (<SAM>) { + last unless (/^@/); +} +my $cnt = 0; +my %hsh = (); +my $pamp = "."; + +#Print header + +print QC "#" . join("\t", qw/chr pos amp dp ntRef ntVar nRef nVar nA nC nG nT nN ins del/) . "\n"; +print QC2 "#" . join("\t", qw/read chr pos amp event/) . "\n"; +print TARGET "#" . join("\t", qw/amp chr start end assayStart assayEnd depth/) . "\n"; +while (<SAM>) { + # Skip stampy reads? Nope, stampy is no longer needed +# next if ($stampy == 1 && ! /XP:Z:BWA/); + chomp; + my @row = split(/\t/, $_); + my $l = 0; + my $cig = $row[5]; + $cig =~ s/(\d+)[MD]/$l+=$1/eg; + + # Check if alignment fits amplicon probes / primers. + my $amp = $hash{$row[2]}{$row[3]}{$l} || next; + + push @{$stats{$amp}{sam}}, [@row]; + $stats{$amp}{depth}++; + if (($pamp ne ".") && ($amp ne $pamp)) { + print STDOUT "Flushing $pamp $stats{$pamp}{depth}\n"; + my $data = &call($stats{$pamp}{sam}); + &flush($data, $stats{$pamp}{chr}, $pamp, $stats{$pamp}{assayStart}, $stats{$pamp}{assayEnd}); + $stats{$pamp}{sam} = []; + } + $pamp = $amp; + $cnt++; +} + +print STDOUT "Flushing $pamp $stats{$pamp}{depth}\n"; +my $data = &call($stats{$pamp}{sam}); +&flush($data, $stats{$pamp}{chr}, $pamp, $stats{$pamp}{assayStart}, $stats{$pamp}{assayEnd}); +$stats{$pamp}{sam} = []; + +close QC; +close QC2; +foreach my $pamp (keys %stats) { + print TARGET join("\t", $pamp, map { $stats{$pamp}{$_} || "NA"} qw/chr start end assayStart assayEnd depth/) . "\n"; +} +close TARGET; +close SAM; + +sub call { + my $SAM = shift; + my $ppos = 0; + my $pchr = ""; + my %data = (); + my $refSeq = ""; + my $c = 0; + my $col_chr = 2; + my $col_read = 9; + my $col_qual = 10; + my $col_pos = 3; + my $col_cigar = 5; + my %cooc = (); + my $cnt = 1; + foreach my $r (0 .. $#$SAM) { + my @row = @{$SAM->[$r]}; + my $read = $row[$col_read]; + my $qual = $row[$col_qual]; + my $pos = $row[$col_pos]; + my @cig = (); + my $aln = 0; + + # Calculate mean read quality and skip if it's below threshold + if ($QavgLim > 0) { + my $QSum = 0; + my $Qlen = length($qual); + + $QSum += ord($qual) foreach 1 .. $Qlen; + + my $Qavg = $QSum / $Qlen - 33; + next if ($Qavg < $QavgLim); + } + + while ($row[$col_cigar] =~ /(\d+)(\D)/g) { + push @cig, [$1, $2]; + $aln += $1; + } + if ($ppos != $pos) { + my $offset = $idx{$row[$col_chr]}->[2]; # Byte offset for chromosome + my $nl = int (($row[$col_pos] - 1) / $idx{$row[$col_chr]}->[3]); # Newline bytes to offset + $offset += $row[$col_pos] + $nl - 50 - 1; # Read in 50 nt prior to start of amplicon + seek REF, $offset, 0; + read REF, $refSeq, 350; + $refSeq =~ s/\s//g; + $data{$row[$col_chr]}{$row[$col_pos] + $_ - 50 + 1}{"refNT"} = substr($refSeq, $_, 1) foreach (0 .. 300); + $ppos = $pos; + } + + foreach my $cigE (@cig) { + my $n = $cigE->[0]; + if ($cigE->[1] eq "I") { + my $insert = $data{$row[$col_chr]}{$pos - 1}{"refNT"}; + $insert .= substr($read, 0, $n, ""); + my $qinsert .= substr($qual, 0, $n, ""); + push @{$data{$row[$col_chr]}{$pos - 1}{"IR"}{$insert}}, $r; + $data{$row[$col_chr]}{$pos - 1}{"I"}{$insert}++; + } + elsif ($cigE->[1] eq "M") { + my $mseq = substr($read, 0, $n, ""); + my $mqual = substr($qual, 0, $n, ""); + foreach my $nt (0 .. (length($mseq) - 1)) { + $data{$row[$col_chr]}{$pos + $nt}{"DP"}++; + my $ntq = substr($mqual, $nt, 1); + my $ntn = substr($mseq, $nt, 1); + if (ord($ntq) - 33 < $Qthreshold) { + $ntn = "N"; + } + $data{$row[$col_chr]}{$pos + $nt}{"NT"}{$ntn}++; + push @{$data{$row[$col_chr]}{$pos + $nt}{"NTR"}{$ntn}}, $r if (uc($ntn) ne uc($data{$row[$col_chr]}{$pos + $nt}{refNT})); + } + $pos += $n; + + } + elsif ($cigE->[1] eq "D") { + my $deletion = join("", map { $data{$row[$col_chr]}{$pos + $_ -1}{"refNT"} } (0 .. ($n))); + push @{$data{$row[$col_chr]}{$pos - 1}{"DR"}{$deletion}}, $r; + $data{$row[$col_chr]}{$pos - 1}{"D"}{$deletion}++; + $pos += $n; + } + } + $cnt++; + } + return \%data; +} + +sub coocCalc { + my $cooc = shift; + my $data = shift; + my $thresh = shift; + my %rev = (); + # Filter low frequency variants + foreach my $k (keys(%$cooc)) { + if (scalar(keys(%{$cooc->{$k}})) < $thresh) { + delete($cooc->{$k}); + next; + } + print STDERR "$k : $thresh : " . join(":", sort {$a cmp $b} keys(%{$cooc->{$k}})) . "\n"; + } + my @muts = keys(%{$cooc}); + foreach my $i (0 .. $#muts) { + foreach my $j (($i + 1) .. $#muts) { + my $score = 0; + foreach my $m (keys(%{$cooc->{$muts[$i]}})) { + if (exists($cooc->{$muts[$j]}{$m})) { + $score++; + } + } + print STDERR $muts[$i] .":". $muts[$j] . ":" . $score . "\n"; sleep 1; + } + } + + sleep 1; +} + +sub flush { + my $data = shift; + my $chr = shift; + my $amp = shift; + my $s = shift; + my $e = shift; + return unless (exists($data->{$chr})); + print STDOUT "printing ... "; + my %reads = (); # read->pos->nt + foreach my $p ($s .. $e) { + my $posdat = $data->{$chr}{$p} || next; + next unless (exists($posdat->{DP})); + my $refNT = uc($posdat->{refNT}); + my @varOrd = sort { $posdat->{NT}{$b} <=> $posdat->{NT}{$a} } grep {$_ ne "N"} grep { $_ ne $refNT } keys(%{$posdat->{NT}}); + my $seqNT = join("/", @varOrd); + my $refCNT = $posdat->{NT}{$refNT} || 0; + my $varCNT = 0; + $varCNT = ($varOrd[0])?$posdat->{NT}{$varOrd[0]}:0; + my $Istr = "."; + my $Dstr = "."; + if ($varOrd[0]) { + $reads{$_}{$p} = "$refNT/$varOrd[0]" foreach (@{$posdat->{NTR}{$varOrd[0]}}); + } + if (exists($posdat->{I})) { + $Istr = join("|", map { $_ . ":" . $posdat->{I}{$_} } keys(%{$posdat->{I}})); + foreach my $I (keys(%{$posdat->{IR}})) { + $reads{$_}{$p} = "$refNT/$I" foreach (@{$posdat->{IR}{$I}}); + } + } + if (exists($posdat->{D})) { + $Dstr = join("|", map { $_ . ":" . $posdat->{D}{$_} } keys(%{$posdat->{D}})); + foreach my $D (keys(%{$posdat->{DR}})) { + $reads{$_}{$p} = "$D/$refNT" foreach (@{$posdat->{DR}{$D}}); + } + } + print QC join("\t", $chr, $p, $amp, + $posdat->{DP} || 0, + $posdat->{refNT} || ".", + $seqNT || ".", + $refCNT, $varCNT, + (map { $posdat->{NT}{$_} || 0 } qw(A C G T N)), $Istr, $Dstr, + ) . "\n"; + } + delete $data->{$chr}; + foreach my $r (sort { $a <=> $b } keys(%reads)) { + print QC2 join("\t", $r, $chr, $_, $amp, $reads{$r}{$_}) . "\n" foreach (sort {$a <=> $b} keys(%{$reads{$r}})); + } + print STDOUT "done\n"; +} +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/qc2vcf.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,140 @@ +#!/usr/bin/perl + +use strict; +use File::Basename; + +my $qc = shift; +my $base = shift || undef; + +unless ($base) { + $base = basename($qc, ".qc.ann.qual.filt.txt") +} + +my $minDp = 100; +my $minVarDp = 5; +my $minVaf = 0.01; + +my $header = qq(##fileformat=VCFv4.1 +##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Depth"> +##FORMAT=<ID=AD,Number=2,Type=Integer,Description="Allele Distribution"> +##FORMAT=<ID=AB,Number=1,Type=Float,Description="Allele Ballance nref/nref+nvar"> +##INFO=<ID=TARGET,Number=1,Type=String,Description="TSACP Target name"> +#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT $base +); + +my $chr = 0; +my $pos = 1; +my $target = 2; +my $dp = 3; +my $ref = 4; +my $var = 5; +my $nref = 6; +my $nvar = 7; +my $nA = 8; +my $nC = 9; +my $nG = 10; +my $nT = 11; +my $nN = 12; +my $ins = 13; +my $del = 14; +my $pval = 15; +my $pvala = 16; +my $varQual = 17; +my $insQual = 18; +my $delQual = 19; + +my %acgt = (A => 0, C => 1, G => 2, T => 3); +print $header; +open QC, "<$qc"; +while (<QC>) { + chomp; + next if (/^#/); + next if (/^X\./); + my @row = split(/\t/, $_); + next if ($row[$target] eq "."); + + my $VAR = substr($row[$var], 0, 1); + my $REF = $row[$ref]; + my $nvarall = $row[$nvar]; + my $indel = $row[$ins] . $row[$del]; + if ($row[$nvar] > 0 || $indel eq "..") { + my %ord = ( A => $row[$nA], C => $row[$nC], G => $row[$nG], T => $row[$nT], N => $row[$nN] ); + $ord{uc($REF)} = -1; # Exclude ref from sort + $ord{N} = -1; # Exclude N! + my @order = sort { $ord{$b} <=> $ord{$a} } keys(%ord); + my $dpVar = $ord{$order[0]}; + my $VAR = $order[0]; + my $skip = 0; + my $tot = $row[$nref] + $dpVar; + my $vaf = ($tot > 0)?$dpVar / $tot:"NA"; # Excluding other alleles... + #$skip++ if ($tot == 0); + #$skip++ if ($ord{$order[0]} == $ord{$order[1]}); # Multiallelic, skipping for now + #$skip++ if ($dpVar == 0); # Skip if dpVar is zero, can occur when N is the only variant. Above line also protects for this. + #$skip++ if ($dpVar < $minVarDp); + #$skip++ if ($row[$dp] < $minDp); + #$skip++ if ($vaf < $minVaf); + my $gt = "$row[$ref]/$VAR"; + my $qual = $row[$varQual] || 0; + $skip++ if ($qual == 0); + my $filter = 0; + my $info = "TARGET=$row[$target]"; + my $format = "DP:AD:AB"; + my $sample = "$row[$dp]:$row[$nref],$dpVar:$vaf"; + print join("\t", @row[$chr, $pos], ".", $REF, $VAR, $qual, $filter, $info, $format, $sample) . "\n" if ($skip == 0); + } + # INDEL + if ($row[$ins] ne ".") { + my $skip = 0; + # Modify coordinte to conform to VCF? + my %inss = split(/[\|\:]/, $row[$ins]); + my @keys = sort { $inss{$b} <=> $inss{$a} } keys %inss; +# if ($inss{$keys[0]} > $row[$nvar]) { +# $nvarall = $inss{$keys[0]}; +# $VAR = $keys[0]; +# $row[$dp] += $nvarall; +# } + my $nins = $inss{$keys[0]}; + my $DP = $row[$dp]; + my $nREF = $DP - $nins; + #$skip++ if ($nins < $minVarDp); + #$skip++ if ($DP < $minDp); + my $vaf = $nins / $row[$dp]; + #$skip++ if ($vaf < $minVaf); + my $gt = "$row[$ref]/$keys[0]"; + my $qual = $row[$insQual]; + $skip++ if ($qual == 0); + my $filter = 0; + my $info = "TARGET=$row[$target]"; + my $format = "DP:AD:AB"; + my $sample = "$DP:$nREF,$nins:$vaf"; + print join("\t", @row[$chr, $pos], ".", $REF, $keys[0], $qual, $filter, $info, $format, $sample) . "\n" if ($skip == 0); + } + if ($row[$del] ne ".") { + my $skip = 0; + # Modify coordinte to conform to VCF? + my %dels = split(/[\|\:]/, $row[$del]); + my @keys = sort { $dels{$b} <=> $dels{$a} } keys %dels; +# if ($dels{$keys[0]} > $row[$nvar]) { +# $nvarall = $dels{$keys[0]}; +# $REF = $keys[0]; +# $row[$dp] += $nvarall; +# } + my $ndel = $dels{$keys[0]}; + my $DP = $row[$dp]; + my $nREF = $DP - $ndel; + #$skip++ if ($ndel < $minVarDp); + #$skip++ if ($DP < $minDp); + my $vaf = $ndel / $DP; + #$skip++ if ($vaf < $minVaf); + my $gt = "$keys[0]/$row[$ref]"; + my $qual = $row[$delQual]; + $skip++ if ($qual == 0); + my $filter = 0; + my $info = "TARGET=$row[$target]"; + my $format = "DP:AD:AB"; + my $sample = "$DP:$nREF,$ndel:$vaf"; + print join("\t", @row[$chr, $pos], ".", $keys[0], $row[$ref], $qual, $filter, $info, $format, $sample) . "\n" if ($skip == 0); + } +} +close QC; +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/qcFilt.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,54 @@ +#!/usr/bin/perl + +use strict; + +my $qcQual = shift; +my $output = shift; + +my $minDp = shift || 100; +my $minVar = shift || 10; +my $minIns = shift || $minVar; +my $minDel = shift || $minVar; +my $minVarQ = shift || 100; +my $minInsQ = shift || 200; +my $minDelQ = shift || 200; + +open QC, "<$qcQual"; +my $head = readline QC; +chomp; +$head =~ s/\s+$//; +my @rhead = split(/\t/, $head); +my $coln = 0; +my %col = map { $_ => $coln++ } @rhead; +open OUT, ">$output.qc.ann.qual.filt.txt"; +print OUT "$head\n"; + +while (<QC>) { + my $line = $_; + my @row = split(/\t/, $_); + my $key = $row[$col{"X.chr"}] . ":" . $row[$col{pos}]; + next if ($row[$col{dp}] < $minDp); + # Var + if ($row[$col{qScore}] >= $minVarQ && $row[$col{nVar}] > $minVar) { + print OUT $line; + next; + } + # Ins + if ($row[$col{qScoreI}] >= $minInsQ) { + $row[$col{ins}] =~ /:(\d+)/; + if ($1 >= $minIns) { + print OUT $line; + next; + } + } + # Del + if ($row[$col{qScoreD}] >= $minDelQ) { + $row[$col{del}] =~ /:(\d+)/; + if ($1 >= $minDel) { + print OUT $line; + next; + } + } +} + +close OUT;
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/splitEff.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,82 @@ +#!/usr/bin/perl -w +# +use strict; +my $file = shift; +my $tag = shift || "NoTag"; + +open F, "<$file"; +my $head = undef; +my %effIdx = (); +$effIdx{context} = 0; +while (<F>) { + if (/.*ID=EFF.*(\(.*\)).*/) { + my $str = $1; +# print STDERR $str . "\n"; + $str =~ s/\[.*\]//g; +# print STDERR $str . "\n"; + $str =~ s/^\(\s*(.*?)\s*\)$/$1/; +# print STDERR $str . "\n"; + my $c = 1; + $effIdx{lc($_)} = $c++ foreach split(/\s*\|\s*/, $str); +# print STDERR join("\n", map { $_ . ":" . $effIdx{$_} } keys(%effIdx)) . "\n"; +# exit; + } + if (/#CHROM/) { + $head = $_; + last; + } + +} + +chomp $head; +my @hrow = split(/\t/, $head); +my $colN = 0; +#my %col = map { print STDERR "$_ => $colN\n";$_ => $colN++ } @hrow; +my %col = map { $_ => $colN++ } @hrow; +# Add AD column +# Convert DP4 for samtools file +my $ADName = (grep { /\_AD/ } keys(%col))[0]; +if (exists($col{DP4})) { + $ADName = "DP4"; +} +my $ADCol = $col{$ADName}; + +my $DPName = (grep { /\_DP/ } keys(%col))[0]; +if (exists($col{DP})) { + $DPName = "DP"; +} +my $DPCol = $col{$DPName}; + +#print STDERR $ADName . "\t" . $col{$ADName} . " $ADCol\n"; + +#Effect_Impact | Functional_Class | Codon_Change | Amino_Acid_change| Amino_Acid_length | Gene_Name | Gene_BioType | Coding | Transcript | Exon [ | ERRORS | WARNINGS ] ) +my @Col = qw/DP AD Context Effect_Impact Functional_Class Codon_Change Amino_Acid_change Amino_Acid_length Gene_Name Transcript_BioType Gene_Coding Transcript_ID Exon_Rank Tag/; + +my @effCol = map {lc} qw/Context Effect_Impact Functional_Class Codon_Change Amino_Acid_change Amino_Acid_length Gene_Name transcript_BioType Gene_Coding Transcript_ID Exon_Rank/; +my @effColOrd = map {$effIdx{$_}} @effCol; + +print join("\t", @hrow[0 ..5], @Col) . "\n"; #map { "eff$_" } 1 .. 10) . "\n"; +while (<F>) { + chomp; + my @row = split(/\t/, $_); + + if ($ADName eq "DP4") { + my @dp4row = split(/,/, $row[$ADCol]); +# print STDERR join(":", @dp4row) . "\n"; sleep 1; + $row[$ADCol] = ($dp4row[0] + $dp4row[1]) . "," . ($dp4row[2] + $dp4row[3]); + } + +# print $row[$col{EFF}] . "\n"; + my @effs = split(/,/, $row[$col{EFF}]); + foreach my $eff (@effs) { + $eff =~ s/\)$//; + my @effrow = split(/[\|\(\)]/, $eff, -1); + +# print STDERR scalar(@effrow) . " $eff\n"; +# print STDERR join(":", @effrow) . " $eff\n"; sleep 1; + print join("\t", @row[0 .. 5, $DPCol, $ADCol], @effrow[@effColOrd], $tag) . "\n"; + + } +} + +close F;
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/lib/perl/vcf2tsv.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,73 @@ +#!/usr/bin/perl -w + +use strict; + +my @vcfs = @ARGV; + +my @info = (); +my @format = (); +my $header = ""; + +foreach my $vcf (0 .. $#vcfs) { + open V, "<$vcfs[$vcf]"; + while (<V>) { + if (/^#CHROM/) { + if ($vcf == 0) { + chomp; + my @row = split(/\t/, $_); + print $header; + print join("\t", @row[0 .. 6], @info) . "\t"; + my @sampleRow = (); + foreach my $s (9 .. $#row) { +# print join("\t", map { "S$s" . "_$_" } @format) . "\n"; + push @sampleRow, map { $row[$s] . "_$_" } @format; + } + print join("\t", @sampleRow) . "\n"; + } + last; + } + if (/^##INFO/ && ($vcf == 0)) { + /ID=(.*?),/; + push @info, $1; + } + elsif (/^##FORMAT/ && ($vcf == 0)) { + /ID=(.*?),/; + push @format, $1; + } + $header .= $_; + } + + while (<V>) { + print join("\t", @{ &readTags(\$_) }) . "\n"; + } + close V; +} + +sub readTags { + my $line = shift; + chomp $$line; + my @row = split(/\t/, $$line); + my @res = (@row[0 .. 6]); + my @infoDat = split(/[;]/, $row[7]); + my @formatDat1 = split(/:/, $row[8]); + my %infoHsh = (); + foreach my $i (@infoDat) { + my @e = split(/=/, $i); + $infoHsh{$e[0]} = defined($e[1])?$e[1]:"1"; + } + + foreach my $t (0 .. $#info) { + push @res, defined($infoHsh{$info[$t]})?$infoHsh{$info[$t]}:"."; + } + + foreach my $s (9 .. $#row) { + my %formatHsh = (); + my @formatDat2 = split(/:/, $row[$s]); + $formatHsh{$formatDat1[$_]} = $formatDat2[$_] foreach (0 .. $#formatDat1); + + foreach my $i (0 .. $#format) { + push @res, defined($formatHsh{$format[$i]})?$formatHsh{$format[$i]}:"."; + } + } + return \@res; +}
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/TSACP.bed Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,221 @@ +chr1 43814981 43815163 MPL1_2.chr1.43815008.43815009_tile_1 100 + 43815005 43815137 +chr1 115256499 115256680 NRAS1_7.chr1.115256528.115256531_tile_1 100 + 115256525 115256653 +chr1 115258701 115258884 NRAS8_13.chr1.115258730.115258748_tile_1 100 + 115258727 115258855 +chr2 29432635 29432822 ALK1.chr2.29432664.29432664_tile_1 100 + 29432662 29432795 +chr2 29443666 29443836 ALK2.chr2.29443695.29443695_tile_1 100 + 29443691 29443810 +chr2 209113083 209113264 IDH1_1_2.chr2.209113112.209113113_tile_1 100 + 209113110 209113237 +chr2 212288911 212289100 ERBB4_1_2.chr2.212288942.212288955_tile_1 100 + 212288938 212289073 +chr2 212530035 212530210 ERBB4_3_4.chr2.212530066.212530135_tile_1 100 + 212530061 212530183 +chr2 212576820 212576990 ERBB4_5.chr2.212576857.212576857_tile_1 100 + 212576850 212576960 +chr2 212578314 212578499 ERBB4_6_7.chr2.212578341.212578349_tile_1 100 + 212578339 212578470 +chr2 212587114 212587285 ERBB4_8.chr2.212587147.212587147_tile_1 100 + 212587141 212587258 +chr2 212589782 212589957 ERBB4_9.chr2.212589811.212589811_tile_1 100 + 212589809 212589930 +chr2 212652705 212652876 ERBB4_10.chr2.212652764.212652764_tile_1 100 + 212652735 212652849 +chr2 212812126 212812311 ERBB4_11.chr2.212812157.212812157_tile_1 100 + 212812155 212812284 +chr3 10183768 10183952 VHL1_2.chr3.10183797.10183817_tile_1 100 + 10183793 10183926 +chr3 10188216 10188401 VHL3_5.chr3.10188245.10188301_tile_1 100 + 10188243 10188374 +chr3 10191449 10191634 VHL6_8.chr3.10191480.10191506_tile_1 100 + 10191477 10191607 +chr3 37067211 37067394 MLH1.chr3.37067240.37067240_tile_1 100 + 37067237 37067367 +chr3 41266009 41266180 CTNNB1_1_16.chr3.41266040.41266137_tile_1 100 + 41266036 41266153 +chr3 178916835 178917024 PIK3CA1.chr3.178916876.178916876_tile_1 100 + 178916861 178916997 +chr3 178921524 178921709 PIK3CA2.chr3.178921553.178921553_tile_1 100 + 178921551 178921682 +chr3 178927905 178928082 PIK3CA3.chr3.178927980.178927980_tile_1 100 + 178927932 178928055 +chr3 178936043 178936214 PIK3CA4_11.chr3.178936074.178936095_tile_1 100 + 178936070 178936187 +chr3 178938831 178939004 PIK3CA12.chr3.178938860.178938860_tile_1 100 + 178938858 178938977 +chr3 178951880 178952054 PIK3CA13_20.chr3.178952007.178952150_tile_1 100 + 178951906 178952026 +chr3 178951998 178952184 PIK3CA13_20.chr3.178952007.178952150_tile_2 100 - 178952025 178952154 +chr4 1803537 1803712 FGFR3_1_2.chr4.1803564.1803568_tile_1 100 + 1803562 1803685 +chr4 1806090 1806277 FGFR3_3_4.chr4.1806119.1806153_tile_1 100 + 1806117 1806250 +chr4 1807835 1808025 FGFR3_5_7.chr4.1807862.1807890_tile_1 100 + 1807857 1807999 +chr4 1808294 1808464 FGFR3_8.chr4.1808331.1808331_tile_1 100 + 1808316 1808442 +chr4 1808920 1809105 FGFR3_9.chr4.1808949.1808949_tile_1 100 + 1808943 1809078 +chr4 55140980 55141157 PDGFRA1_4.chr4.55141013.55141049_tile_1 100 + 55141007 55141130 +chr4 55144119 55144306 PDGFRA5.chr4.55144146.55144146_tile_1 100 + 55144145 55144279 +chr4 55144518 55144703 PDGFRA6.chr4.55144547.55144547_tile_1 100 + 55144544 55144676 +chr4 55152011 55152184 PDGFRA7_23.chr4.55152040.55152109_tile_1 100 + 55152036 55152157 +chr4 55561735 55561913 KIT1.chr4.55561764.55561764_tile_1 100 + 55561762 55561887 +chr4 55592154 55592341 KIT2.chr4.55592185.55592186_tile_1 100 + 55592180 55592314 +chr4 55593341 55593512 KIT3_19.chr4.55593464.55593689_tile_1 100 + 55593365 55593483 +chr4 55593435 55593609 KIT3_19.chr4.55593464.55593689_tile_2 100 - 55593461 55593583 +chr4 55593555 55593739 KIT3_19.chr4.55593464.55593689_tile_3 100 + 55593582 55593713 +chr4 55594192 55594380 KIT20_21.chr4.55594221.55594258_tile_1 100 + 55594219 55594352 +chr4 55595492 55595675 KIT22.chr4.55595519.55595519_tile_1 100 + 55595518 55595646 +chr4 55597466 55597652 KIT23.chr4.55597495.55597497_tile_1 100 + 55597493 55597624 +chr4 55599289 55599472 KIT24_28.chr4.55599320.55599348_tile_1 100 + 55599316 55599445 +chr4 55602665 55602850 KIT29.chr4.55602694.55602694_tile_1 100 + 55602690 55602823 +chr4 55945983 55946155 KDR1.chr4.55946114.55946257_tile_1 100 + 55946013 55946125 +chr4 55946097 55946284 KDR1.chr4.55946114.55946257_tile_2 100 - 55946124 55946257 +chr4 55953776 55953965 KDR3.chr4.55953807.55953807_tile_1 100 + 55953803 55953938 +chr4 55955084 55955257 KDR4.chr4.55955111.55955127_tile_1 100 + 55955108 55955230 +chr4 55960958 55961129 KDR6.chr4.55960989.55961023_tile_1 100 + 55960985 55961102 +chr4 55962476 55962653 KDR8.chr4.55962507.55962507_tile_1 100 + 55962502 55962626 +chr4 55972935 55973106 KDR9.chr4.55972964.55972964_tile_1 100 + 55972962 55973079 +chr4 55979594 55979775 KDR10.chr4.55979623.55979623_tile_1 100 + 55979620 55979748 +chr4 55980319 55980496 KDR11.chr4.55980348.55980348_tile_1 100 + 55980346 55980469 +chr4 153245415 153245604 FBXW7_1.chr4.153245446.153245446_tile_1 100 + 153245442 153245575 +chr4 153247247 153247417 FBXW7_2.chr4.153247288.153247366_tile_1 100 + 153247277 153247389 +chr4 153249337 153249520 FBXW7_5.chr4.153249384.153249384_tile_1 100 + 153249364 153249493 +chr4 153250852 153251031 FBXW7_7.chr4.153250883.153250883_tile_1 100 + 153250878 153251004 +chr4 153258952 153259142 FBXW7_8.chr4.153258983.153258983_tile_1 100 + 153258980 153259112 +chr5 112173886 112174071 APC1.chr5.112173917.112173917_tile_1 100 + 112173913 112174044 +chr5 112174602 112174775 APC2.chr5.112174631.112174631_tile_1 100 + 112174629 112174748 +chr5 112175033 112175208 APC3_42.chr5.112175162.112175958_tile_1 100 - 112175061 112175181 +chr5 112175127 112175297 APC3_42.chr5.112175162.112175958_tile_2 100 + 112175154 112175273 +chr5 112175215 112175386 APC3_42.chr5.112175162.112175958_tile_3 100 - 112175243 112175361 +chr5 112175305 112175475 APC3_42.chr5.112175162.112175958_tile_4 100 + 112175335 112175447 +chr5 112175393 112175566 APC3_42.chr5.112175162.112175958_tile_5 100 - 112175419 112175539 +chr5 112175511 112175683 APC3_42.chr5.112175162.112175958_tile_6 100 + 112175537 112175657 +chr5 112175629 112175799 APC3_42.chr5.112175162.112175958_tile_7 100 - 112175656 112175771 +chr5 112175739 112175911 APC3_42.chr5.112175162.112175958_tile_8 100 + 112175769 112175881 +chr5 112175853 112176042 APC3_42.chr5.112175162.112175958_tile_9 100 - 112175880 112176015 +chr5 149433615 149433799 CSF1R1_3.chr5.149433644.149433646_tile_1 100 + 149433642 149433773 +chr5 149453015 149453189 CSF1R4.chr5.149453044.149453044_tile_1 100 + 149453042 149453163 +chr5 170837492 170837677 NPM1.chr5.170837547.170837548_tile_1 100 + 170837518 170837650 +chr7 55211051 55211238 EGFR1.chr7.55211080.55211080_tile_1 100 + 55211078 55211211 +chr7 55221791 55221964 EGFR2.chr7.55221822.55221822_tile_1 100 + 55221817 55221937 +chr7 55233018 55233203 EGFR3.chr7.55233043.55233043_tile_1 100 + 55233041 55233176 +chr7 55241648 55241827 EGFR4.chr7.55241677.55241708_tile_1 100 + 55241674 55241800 +chr7 55242387 55242576 EGFR9.chr7.55242418.55242511_tile_1 100 + 55242415 55242549 +chr7 55248878 55249052 EGFR44.chr7.55249005.55249131_tile_1 100 + 55248904 55249026 +chr7 55249002 55249178 EGFR44.chr7.55249005.55249131_tile_2 100 - 55249025 55249152 +chr7 55259485 55259662 EGFR54.chr7.55259514.55259524_tile_1 100 + 55259512 55259635 +chr7 116339613 116339792 MET1.chr7.116339642.116339642_tile_1 100 + 116339640 116339765 +chr7 116340233 116340420 MET2.chr7.116340262.116340262_tile_1 100 + 116340260 116340393 +chr7 116411957 116412127 MET3.chr7.116411990.116411990_tile_1 100 + 116411983 116412099 +chr7 116417430 116417620 MET4.chr7.116417463.116417464_tile_1 100 + 116417457 116417592 +chr7 116423384 116423555 MET6.chr7.116423413.116423474_tile_1 100 + 116423410 116423528 +chr7 128845072 128845257 SMO1.chr7.128845101.128845101_tile_1 100 + 128845096 128845232 +chr7 128846009 128846194 SMO2.chr7.128846040.128846040_tile_1 100 + 128846036 128846167 +chr7 128846347 128846536 SMO3.chr7.128846374.128846374_tile_1 100 + 128846372 128846509 +chr7 128850310 128850499 SMO4.chr7.128850341.128850341_tile_1 100 + 128850334 128850472 +chr7 128851562 128851734 SMO5.chr7.128851593.128851593_tile_1 100 + 128851589 128851708 +chr7 140453092 140453267 BRAF1.chr7.140453121.140453193_tile_1 100 + 140453118 140453240 +chr7 140481368 140481545 BRAF28.chr7.140481397.140481478_tile_1 100 + 140481395 140481518 +chr8 38282182 38282360 FGFR1_1.chr8.38282209.38282209_tile_1 100 + 38282207 38282334 +chr8 38285907 38286090 FGFR1_2.chr8.38285938.38285938_tile_1 100 + 38285934 38286063 +chr9 5073736 5073923 JAK2_1.chr9.5073769.5073770_tile_1 100 + 5073764 5073894 +chr9 21971122 21971308 CDKN2A1.chr9.21971153.21971187_tile_1 100 + 21971147 21971282 +chr9 133738301 133738491 ABL1_1.chr9.133738330.133738364_tile_1 100 + 133738327 133738465 +chr9 133747475 133747664 ABL1_9.chr9.133747520.133747520_tile_1 100 + 133747502 133747641 +chr9 133748156 133748327 ABL1_10.chr9.133748283.133748414_tile_1 100 - 133748186 133748302 +chr9 133748276 133748457 ABL1_10.chr9.133748283.133748414_tile_2 100 + 133748301 133748434 +chr9 133750327 133750516 ABL1_16.chr9.133750356.133750356_tile_1 100 + 133750351 133750489 +chr9 139397739 139397928 NOTCH1_1.chr9.139397768.139397768_tile_1 100 + 139397765 139397901 +chr9 139399315 139399485 NOTCH1_2.chr9.139399344.139399422_tile_1 100 + 139399341 139399459 +chr10 43609047 43609226 RET1.chr10.43609078.43609104_tile_1 100 + 43609073 43609201 +chr10 43609901 43610075 RET2_9.chr10.43609940.43609950_tile_1 100 - 43609929 43610049 +chr10 43613809 43613998 RET10.chr10.43613840.43613840_tile_1 100 + 43613832 43613971 +chr10 43615532 43615703 RET11_12.chr10.43615567.43615569_tile_1 100 + 43615560 43615678 +chr10 43617387 43617564 RET13.chr10.43617416.43617416_tile_1 100 + 43617414 43617537 +chr10 89624213 89624388 PTEN1.chr10.89624242.89624244_tile_1 100 + 89624240 89624361 +chr10 89685274 89685459 PTEN3.chr10.89685307.89685307_tile_1 100 + 89685303 89685432 +chr10 89711864 89712039 PTEN4.chr10.89711893.89711900_tile_1 100 + 89711890 89712012 +chr10 89717488 89717668 PTEN7.chr10.89717615.89717772_tile_1 100 + 89717514 89717638 +chr10 89717614 89717801 PTEN7.chr10.89717615.89717772_tile_2 100 - 89717637 89717772 +chr10 89720683 89720870 PTEN13.chr10.89720716.89720852_tile_1 100 + 89720708 89720843 +chr10 89720813 89720991 PTEN13.chr10.89720716.89720852_tile_2 100 - 89720842 89720961 +chr10 123258005 123258184 FGFR2_1.chr10.123258034.123258034_tile_1 100 + 123258032 123258157 +chr10 123274745 123274930 FGFR2_2.chr10.123274774.123274803_tile_1 100 + 123274772 123274903 +chr10 123279384 123279555 FGFR2_5.chr10.123279503.123279677_tile_1 100 + 123279411 123279528 +chr10 123279470 123279640 FGFR2_5.chr10.123279503.123279677_tile_2 100 - 123279498 123279614 +chr10 123279586 123279769 FGFR2_5.chr10.123279503.123279677_tile_3 100 + 123279613 123279742 +chr11 533842 534021 HRAS1.chr11.533873.533875_tile_1 100 + 533868 533994 +chr11 534250 534434 HRAS6.chr11.534285.534289_tile_1 100 + 534277 534410 +chr11 108117816 108117989 ATM1.chr11.108117847.108117848_tile_1 100 + 108117845 108117962 +chr11 108119792 108119963 ATM2.chr11.108119823.108119823_tile_1 100 + 108119819 108119936 +chr11 108123512 108123683 ATM3.chr11.108123551.108123551_tile_1 100 + 108123541 108123654 +chr11 108137938 108138126 ATM4.chr11.108137973.108138003_tile_1 100 + 108137967 108138096 +chr11 108155103 108155281 ATM6.chr11.108155132.108155132_tile_1 100 + 108155130 108155251 +chr11 108170441 108170618 ATM7.chr11.108170476.108170479_tile_1 100 + 108170468 108170591 +chr11 108172390 108172571 ATM9.chr11.108172421.108172421_tile_1 100 + 108172417 108172544 +chr11 108173611 108173801 ATM10.chr11.108173640.108173640_tile_1 100 + 108173635 108173771 +chr11 108180914 108181101 ATM11.chr11.108180945.108180945_tile_1 100 + 108180942 108181074 +chr11 108200925 108201096 ATM12.chr11.108200958.108200961_tile_1 100 + 108200954 108201069 +chr11 108204650 108204823 ATM14.chr11.108204681.108204681_tile_1 100 + 108204679 108204796 +chr11 108205738 108205928 ATM15.chr11.108205769.108205769_tile_1 100 + 108205766 108205900 +chr11 108206565 108206750 ATM16.chr11.108206594.108206594_tile_1 100 + 108206592 108206723 +chr11 108218060 108218247 ATM17.chr11.108218089.108218089_tile_1 100 + 108218087 108218220 +chr11 108225561 108225751 ATM18.chr11.108225590.108225590_tile_1 100 + 108225588 108225725 +chr11 108236057 108236241 ATM19.chr11.108236086.108236203_tile_1 100 + 108236084 108236215 +chr12 25378531 25378717 KRAS1.chr12.25378562.25378562_tile_1 100 + 25378558 25378689 +chr12 25380244 25380427 KRAS2.chr12.25380275.25380283_tile_1 100 + 25380270 25380398 +chr12 25398224 25398414 KRAS7.chr12.25398255.25398285_tile_1 100 + 25398253 25398386 +chr12 112888134 112888323 PTPN11_1.chr12.112888163.112888211_tile_1 100 + 112888160 112888296 +chr12 112926855 112927032 PTPN11_10.chr12.112926884.112926888_tile_1 100 + 112926881 112927005 +chr12 121431384 121431558 HNF1A_1.chr12.121431413.121431414_tile_1 100 + 121431410 121431532 +chr12 121432041 121432221 HNF1A_3.chr12.121432070.121432070_tile_1 100 + 121432065 121432195 +chr13 28592589 28592766 FLT3_1.chr13.28592620.28592653_tile_1 100 + 28592617 28592739 +chr13 28602294 28602464 FLT3_13.chr13.28602329.28602329_tile_1 100 + 28602320 28602436 +chr13 28608213 28608402 FLT3_14.chr13.28608244.28608341_tile_1 100 + 28608242 28608375 +chr13 28610097 28610267 FLT3_22.chr13.28610138.28610138_tile_1 100 - 28610122 28610239 +chr13 48919155 48919336 RB1_1.chr13.48919244.48919244_tile_1 100 + 48919185 48919309 +chr13 48923119 48923296 RB1_2.chr13.48923148.48923148_tile_1 100 + 48923146 48923269 +chr13 48942654 48942826 RB1_3.chr13.48942685.48942685_tile_1 100 + 48942683 48942798 +chr13 48955503 48955684 RB1_4.chr13.48955538.48955550_tile_1 100 + 48955532 48955657 +chr13 49027111 49027288 RB1_6.chr13.49027168.49027168_tile_1 100 + 49027140 49027261 +chr13 49033812 49033989 RB1_7.chr13.49033843.49033846_tile_1 100 + 49033839 49033962 +chr13 49037814 49037985 RB1_8.chr13.49037877.49037877_tile_1 100 + 49037844 49037958 +chr13 49039131 49039304 RB1_9.chr13.49039164.49039164_tile_1 100 + 49039158 49039277 +chr14 105246428 105246600 AKT1.chr14.105246455.105246455_tile_1 100 + 105246452 105246574 +chr16 68835612 68835782 CDH1_1.chr16.68835649.68835650_tile_1 100 + 68835638 68835760 +chr16 68846108 68846283 CDH1_2.chr16.68846137.68846137_tile_1 100 + 68846135 68846256 +chr16 68847245 68847422 CDH1_3.chr16.68847274.68847277_tile_1 100 + 68847272 68847395 +chr17 7573976 7574147 TP53_1.chr17.7574003.7574021_tile_1 100 + 7574001 7574120 +chr17 7576995 7577166 TP53_3.chr17.7577022.7577129_tile_1 100 + 7577020 7577139 +chr17 7577494 7577683 TP53_17.chr17.7577523.7577574_tile_1 100 + 7577521 7577656 +chr17 7578063 7578234 TP53_31_59.chr17.7578190.7578536_tile_1 100 + 7578091 7578207 +chr17 7578155 7578325 TP53_31_59.chr17.7578190.7578536_tile_2 100 - 7578180 7578303 +chr17 7578245 7578415 TP53_31_59.chr17.7578190.7578536_tile_3 100 + 7578273 7578389 +chr17 7578345 7578515 TP53_31_59.chr17.7578190.7578536_tile_4 100 - 7578373 7578491 +chr17 7578467 7578645 TP53_31_59.chr17.7578190.7578536_tile_5 100 + 7578490 7578619 +chr17 7579323 7579507 TP53_60.chr17.7579358.7579403_tile_1 100 + 7579350 7579481 +chr17 7579851 7580032 TP53_64.chr17.7579882.7579882_tile_1 100 + 7579878 7580005 +chr17 37880190 37880361 ERBB2_1.chr17.37880219.37880261_tile_1 100 + 37880216 37880334 +chr17 37880962 37881151 ERBB2_4.chr17.37880993.37881012_tile_1 100 + 37880986 37881124 +chr17 37881297 37881482 ERBB2_13.chr17.37881332.37881440_tile_1 100 + 37881324 37881455 +chr18 48575130 48575301 SMAD4_1.chr18.48575169.48575170_tile_1 100 + 48575160 48575272 +chr18 48581167 48581346 SMAD4_2.chr18.48581198.48581198_tile_1 100 + 48581195 48581319 +chr18 48584527 48584714 SMAD4_3.chr18.48584560.48584560_tile_1 100 + 48584553 48584687 +chr18 48586233 48586416 SMAD4_4.chr18.48586262.48586262_tile_1 100 + 48586260 48586389 +chr18 48591795 48591982 SMAD4_5.chr18.48591826.48591919_tile_1 100 + 48591822 48591955 +chr18 48593376 48593547 SMAD4_11.chr18.48593405.48593405_tile_1 100 + 48593402 48593520 +chr18 48602997 48603168 SMAD4_12.chr18.48603032.48603094_tile_1 100 + 48603025 48603139 +chr18 48604637 48604808 SMAD4_15.chr18.48604668.48604754_tile_1 100 + 48604663 48604781 +chr19 1206992 1207169 STK11_1.chr19.1207021.1207092_tile_1 100 + 1207019 1207142 +chr19 1220458 1220638 STK11_4.chr19.1220487.1220502_tile_1 100 + 1220484 1220614 +chr19 1221231 1221407 STK11_8.chr19.1221264.1221319_tile_1 100 - 1221259 1221381 +chr19 1223034 1223221 STK11_12.chr19.1223059.1223125_tile_1 100 + 1223057 1223196 +chr19 17945665 17945840 JAK3_1.chr19.17945696.17945696_tile_1 100 + 17945690 17945813 +chr19 17947980 17948169 JAK3_2.chr19.17948009.17948009_tile_1 100 + 17948004 17948142 +chr20 36031733 36031923 SRC.chr20.36031762.36031762_tile_1 100 + 36031760 36031895 +chr20 57484389 57484560 GNAS1.chr20.57484420.57484421_tile_1 100 + 57484416 57484533 +chr22 24133938 24134126 SMARCB1_1.chr22.24133967.24133990_tile_1 100 + 24133964 24134100 +chr22 24143209 24143383 SMARCB1_3.chr22.24143240.24143240_tile_1 100 + 24143235 24143357 +chr22 24145551 24145726 SMARCB1_4.chr22.24145582.24145582_tile_1 100 + 24145577 24145699 +chr22 24176323 24176495 SMARCB1_5_6.chr22.24176352.24176357_tile_1 100 + 24176350 24176469 +chr19 3114823 3115004 GNA11_4.chr19.3114942.3115070_tile_1 100 - 3114845 3114981 +chr19 3114957 3115133 GNA11_4.chr19.3114942.3115070_tile_2 100 + 3114980 3115111 +chr19 3118801 3118989 GNA11_5.chr19.3118922.3119051_tile_1 100 - 3118825 3118963 +chr19 3119207 3119395 GNA11_6.chr19.3119204.3119357_tile_2 100 - 3119232 3119373 +chr19 3120864 3121035 GNA11_7.chr19.3120987.3121177_tile_1 100 + 3120887 3121008 +chr19 3120984 3121170 GNA11_7.chr19.3120987.3121177_tile_2 100 - 3121006 3121144 +chr19 3121120 3121304 GNA11_7.chr19.3120987.3121177_tile_3 100 + 3121143 3121280 +chr9 80412405 80412592 GNAQ_4.chr9.80412436.80412564_tile_1 100 + 80412432 80412565 +chr9 80409248 80409421 GNAQ_5.chr9.80409379.80409508_tile_1 100 + 80409278 80409392 +chr9 80409334 80409510 GNAQ_5.chr9.80409379.80409508_tile_2 100 - 80409364 80409486 +chr9 80409458 80409639 GNAQ_5.chr9.80409379.80409508_tile_3 100 + 80409485 80409612 +chr9 80343305 80343476 GNAQ_6.chr9.80343430.80343583_tile_1 100 + 80343330 80343447 +chr9 80343391 80343561 GNAQ_6.chr9.80343430.80343583_tile_2 100 - 80343417 80343531 +chr9 80343503 80343689 GNAQ_6.chr9.80343430.80343583_tile_3 100 + 80343530 80343659 +chr9 80336109 80336280 GNAQ_7.chr9.80336240.80336429_tile_1 100 + 80336139 80336255 +chr9 80336203 80336374 GNAQ_7.chr9.80336240.80336429_tile_2 100 - 80336228 80336347 +chr9 80336319 80336495 GNAQ_7.chr9.80336240.80336429_tile_3 100 + 80336346 80336467 +chr22 17052963 17053133 PIK3CA4_11.chr3.178936074.178936095_tile_1 100 + 17052990 17053106 +chr22 17055412 17055585 PIK3CA12.chr3.178938860.178938860_tile_1 100 + 17055439 17055558 +chr9 33675956 33676480 PTEN7.chr10.89717615.89717772_tile_1 100 - 33675986 33676451 +chr9 33675628 33675815 PTEN13.chr10.89720716.89720852_tile_1 100 - 33675655 33675790 +chr7 65970149 65970483 GNA11_6.chr19.3119204.3119357_tile_2 100 + 65970175 65970458 +chr7 65970284 65970719 GNA11_7.chr19.3120987.3121177_tile_1 100 - 65970311 65970696 +chr2 132181237 132181750 GNAQ_5.chr9.80409379.80409508_tile_1 100 + 132181267 132181721 +chr2 132181447 132181600 GNAQ_6.chr9.80343430.80343583_tile_1 100 + 132181474 132181571 +chr2 132181331 132181839 GNAQ_7.chr9.80336240.80336429_tile_2 100 - 132181356 132181815
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/TruSeq_Amplicon_Cancer_Panel_Manifest_AFP1_PN15032433.txt Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,445 @@ +[Header] +Customer Name "ILLUMINA, INC." +Product Type 15032433 +Date Manufactured +Lot +DesignStudio ID NA +Target Plexity 212 + +[Probes] +Target Region Name Target Region ID Target ID Species Build ID Chromosome Start Position End Position Submitted Target Region Strand ULSO Sequence ULSO Genomic Hits DLSO Sequence DLSO Genomic Hits Probe Strand Designer Design Score Expected Amplifed Region Size SNP Masking Labels +MPL1_2 MPL1_2.chr1.43815008.43815009 MPL1_2.chr1.43815008.43815009_tile_1 Homo sapiens hg19 chr1 43815008 43815009 - AAGTGGCGAAGCCGTAGGTGCGCACG 0 TCAGCAGCAGCAGGCCCAGGACGG 0 - ILLUMINA NA 183 TRUE +NRAS1_7 NRAS1_7.chr1.115256528.115256531 NRAS1_7.chr1.115256528.115256531_tile_1 Homo sapiens hg19 chr1 115256528 115256531 - CAATAGCATTGCATTCCCTGTGGTTTT 0 AGAGTACAGTGCCATGAGAGACCAAT 0 - ILLUMINA NA 182 TRUE +NRAS8_13 NRAS8_13.chr1.115258730.115258748 NRAS8_13.chr1.115258730.115258748_tile_1 Homo sapiens hg19 chr1 115258730 115258748 - GGGTTTTCATTTCCATTGATTATAGAAAG 0 CTGACAATCCAGCTAATCCAGAACCA 0 - ILLUMINA NA 184 TRUE +ALK1 ALK1.chr2.29432664.29432664 ALK1.chr2.29432664.29432664_tile_1 Homo sapiens hg19 chr2 29432664 29432664 - GATAAAATCCTAGTGATGGCCGTTGTA 0 GACATCTACAGGTGAGTAAAGACTGCC 0 - ILLUMINA NA 188 TRUE +ALK2 ALK2.chr2.29443695.29443695 ALK2.chr2.29443695.29443695_tile_1 Homo sapiens hg19 chr2 29443695 29443695 - TGCTGCCCATGTTTACAGAATGCCTT 0 CACCAGAACATTGTTCGCTGCATTG 0 - ILLUMINA NA 171 TRUE +IDH1_1_2 IDH1_1_2.chr2.209113112.209113113 IDH1_1_2.chr2.209113112.209113113_tile_1 Homo sapiens hg19 chr2 209113112 209113113 - GAGGGTTGAGGAGTTCAAGTTGAAACA 0 CATGCTTATGGGGATCAAGTAAGTCAT 0 - ILLUMINA NA 182 TRUE +ERBB4_1_2 ERBB4_1_2.chr2.212288942.212288955 ERBB4_1_2.chr2.212288942.212288955_tile_1 Homo sapiens hg19 chr2 212288942 212288955 - ACTACTGGTATAGTGCTGGTTTGTTCA 0 AGAACGTTTGCCTCAGCCTCCCATCTG 0 - ILLUMINA NA 190 TRUE +ERBB4_3_4 ERBB4_3_4.chr2.212530066.212530135 ERBB4_3_4.chr2.212530066.212530135_tile_1 Homo sapiens hg19 chr2 212530066 212530135 - CATTTCAGGGTCCTGACAACTGTACAA 0 AACTGCACCCAAGGGTAAGCATTCTT 0 - ILLUMINA NA 176 TRUE +ERBB4_5 ERBB4_5.chr2.212576857.212576857 ERBB4_5.chr2.212576857.212576857_tile_1 Homo sapiens hg19 chr2 212576857 212576857 - ATACTCTGCTATTTTATAATGAAGATGCAA 0 CCAGTAACATTGACAAATTCATAAACTGTA 0 - ILLUMINA NA 171 TRUE +ERBB4_6_7 ERBB4_6_7.chr2.212578341.212578349 ERBB4_6_7.chr2.212578341.212578349_tile_1 Homo sapiens hg19 chr2 212578341 212578349 - AGGGTAAGATACATAAACACTATCAATGA 0 TGCCTGCCCTAGTTCCAAGATGGAA 0 - ILLUMINA NA 186 TRUE +ERBB4_8 ERBB4_8.chr2.212587147.212587147 ERBB4_8.chr2.212587147.212587147_tile_1 Homo sapiens hg19 chr2 212587147 212587147 - TGAAAGTAATATTTGCTGTGTTGCAGG 0 CATTCTGTGTCAAGAAATGTCCACGTA 0 - ILLUMINA NA 172 TRUE +ERBB4_9 ERBB4_9.chr2.212589811.212589811 ERBB4_9.chr2.212589811.212589811_tile_1 Homo sapiens hg19 chr2 212589811 212589811 - GCAGACTTTGATCATGGTCCTATCTCT 0 GACTGCTTTGTATGTCTGTGATTTCTC 0 - ILLUMINA NA 176 TRUE +ERBB4_10 ERBB4_10.chr2.212652764.212652764 ERBB4_10.chr2.212652764.212652764_tile_1 Homo sapiens hg19 chr2 212652764 212652764 - AATGGTGGAGTCTATGTAGACCAGAAC 0 TCTTTTTAATTTCTCAAAATGTTCTACCCT 0 - ILLUMINA NA 172 TRUE +ERBB4_11 ERBB4_11.chr2.212812157.212812157 ERBB4_11.chr2.212812157.212812157_tile_1 Homo sapiens hg19 chr2 212812157 212812157 - GTGGCTCTTAATCAGTTTCGTTACCTG 0 GGTAAGGAATATATCCAAAATGGCAAATA 0 - ILLUMINA NA 186 TRUE +VHL1_2 VHL1_2.chr3.10183797.10183817 VHL1_2.chr3.10183797.10183817_tile_1 Homo sapiens hg19 chr3 10183797 10183817 - AAAATGGACCCCGGGGCGGTAGAGGG 0 ATACGGGCAGCACGACGCGCGGACT 0 - ILLUMINA NA 185 TRUE +VHL3_5 VHL3_5.chr3.10188245.10188301 VHL3_5.chr3.10188245.10188301_tile_1 Homo sapiens hg19 chr3 10188245 10188301 - GAACTGGGCTTAATTTTTCAAGTGGTC 0 AGAAGCCCATCGTGTGTCCCTGCATCT 0 - ILLUMINA NA 186 TRUE +VHL6_8 VHL6_8.chr3.10191480.10191506 VHL6_8.chr3.10191480.10191506_tile_1 Homo sapiens hg19 chr3 10191480 10191506 - TTGATGTGCAATGCGCTCCTGTGTCAG 0 GTATACACTGGAAGGGCAAAAACCAAAT 0 - ILLUMINA NA 186 TRUE +MLH1 MLH1.chr3.37067240.37067240 MLH1.chr3.37067240.37067240_tile_1 Homo sapiens hg19 chr3 37067240 37067240 - TGGGAGTTCAAGCATCTCCTCATCTTG 0 ATCTGGTGGGCATAGACCTTATCACT 0 - ILLUMINA NA 184 TRUE +CTNNB1_1_16 CTNNB1_1_16.chr3.41266040.41266137 CTNNB1_1_16.chr3.41266040.41266137_tile_1 Homo sapiens hg19 chr3 41266040 41266137 - GGTATCCACATCCTCTTCCTCAGGATT 0 GTCCAACTCCATCAAATCAGCTATAAA 0 - ILLUMINA NA 172 TRUE +PIK3CA1 PIK3CA1.chr3.178916876.178916876 PIK3CA1.chr3.178916876.178916876_tile_1 Homo sapiens hg19 chr3 178916876 178916876 - AGGGACAACAGTTAAGCTTTATGGTTA 0 AAAAATTCTTCCCTTTCTGCTTCTTG 0 - ILLUMINA NA 190 TRUE +PIK3CA2 PIK3CA2.chr3.178921553.178921553 PIK3CA2.chr3.178921553.178921553_tile_1 Homo sapiens hg19 chr3 178921553 178921553 - ACATTCGGAGATTTGGATGTTCTCCTA 0 TCACGTAGGTTGCACAAAGAATTTTTA 0 - ILLUMINA NA 186 TRUE +PIK3CA3 PIK3CA3.chr3.178927980.178927980 PIK3CA3.chr3.178927980.178927980_tile_1 Homo sapiens hg19 chr3 178927980 178927980 - CTTCTAATCCATGAGGTACTGGCCAAA 0 AACACATTTCAAAACACTTTTCTTCCC 0 - ILLUMINA NA 178 TRUE +PIK3CA4_11 PIK3CA4_11.chr3.178936074.178936095 PIK3CA4_11.chr3.178936074.178936095_tile_1 Homo sapiens hg19 chr3 178936074 178936095 - GGTATGGTAAAAACATGCTGAGATCAG 0 CTCGTGTAGAAATTGCTTTGAGCTGTT 0 - ILLUMINA NA 172 TRUE +PIK3CA12 PIK3CA12.chr3.178938860.178938860 PIK3CA12.chr3.178938860.178938860_tile_1 Homo sapiens hg19 chr3 178938860 178938860 - TAAACAACTCTGCCCCACTGCAGTGAA 0 CTTCAAATACATCCCACATGCACGACA 0 - ILLUMINA NA 174 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_1 Homo sapiens hg19 chr3 178952007 178952150 - CCAAAGCCTCTTGCTCAGTTTTATCTAA 0 AGCCTTGTAACACATCTCCTGAAACC 0 - ILLUMINA NA 175 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_2 Homo sapiens hg19 chr3 178952007 178952150 + CATTGCATACATTCGAAAGACCCTAGC 0 AGATAACTGAGAAAATGAAAGCTCACTCTG 0 + ILLUMINA NA 187 TRUE +FGFR3_1_2 FGFR3_1_2.chr4.1803564.1803568 FGFR3_1_2.chr4.1803564.1803568_tile_1 Homo sapiens hg19 chr4 1803564 1803568 - TTGCTGCCATTCACCTCCACGTGCTTG 0 TCTGTGGGGGCAGATGACGCTCAGG 0 - ILLUMINA NA 176 TRUE +FGFR3_3_4 FGFR3_3_4.chr4.1806119.1806153 FGFR3_3_4.chr4.1806119.1806153_tile_1 Homo sapiens hg19 chr4 1806119 1806153 - GCTCAGAACCTGGTATCTACTTTCTGT 0 TAGCTGAGGATGCCTGCATACACACTG 0 - ILLUMINA NA 188 TRUE +FGFR3_5_7 FGFR3_5_7.chr4.1807862.1807890 FGFR3_5_7.chr4.1807862.1807890_tile_1 Homo sapiens hg19 chr4 1807862 1807890 - AAACAAGGCCTCAGGCGCCATCCACT 0 GCCAGCCCGAAGTCTGCGATCT 0 - ILLUMINA NA 191 TRUE +FGFR3_8 FGFR3_8.chr4.1808331.1808331 FGFR3_8.chr4.1808331.1808331_tile_1 Homo sapiens hg19 chr4 1808331 1808331 - CCGGAGGGACCCCCACCCCTGA 0 CCCCCAGCGTGAAGATCTCCCA 0 - ILLUMINA NA 171 TRUE +FGFR3_9 FGFR3_9.chr4.1808949.1808949 FGFR3_9.chr4.1808949.1808949_tile_1 Homo sapiens hg19 chr4 1808949 1808949 - AAGCTCTGTGTAGCTGTCTCTCCATCT 0 TCGTGGGCAAACACGGAGTCGTC 0 - ILLUMINA NA 186 TRUE +PDGFRA1_4 PDGFRA1_4.chr4.55141013.55141049 PDGFRA1_4.chr4.55141013.55141049_tile_1 Homo sapiens hg19 chr4 55141013 55141049 - TACCCCATGGAACTTACCAAGCACTAG 0 CTATAAATGACCAGGACAGGTAACTGG 0 - ILLUMINA NA 178 TRUE +PDGFRA5 PDGFRA5.chr4.55144146.55144146 PDGFRA5.chr4.55144146.55144146_tile_1 Homo sapiens hg19 chr4 55144146 55144146 - GTCAGCTCCATTCAAGGGACTTCTATT 0 TACAATGTTCAAATGTGGCCCCAGGT 0 - ILLUMINA NA 188 TRUE +PDGFRA6 PDGFRA6.chr4.55144547.55144547 PDGFRA6.chr4.55144547.55144547_tile_1 Homo sapiens hg19 chr4 55144547 55144547 - AACATCTCTCTTTGCACCCACCTCCGT 0 ATGATGTAAATGGGGCCTATGGGGAC 0 - ILLUMINA NA 186 TRUE +PDGFRA7_23 PDGFRA7_23.chr4.55152040.55152109 PDGFRA7_23.chr4.55152040.55152109_tile_1 Homo sapiens hg19 chr4 55152040 55152109 - AGAGATTAAAGTGAAGGAGGATGAGCC 0 TTGCGAGCAGCCAGATCACGGTGGA 0 - ILLUMINA NA 174 TRUE +KIT1 KIT1.chr4.55561764.55561764 KIT1.chr4.55561764.55561764_tile_1 Homo sapiens hg19 chr4 55561764 55561764 - GTGTTTGTTGGTGCACGTGTATTTGC 0 CCCACGCGGACTATTAAGTCTGATTTT 0 - ILLUMINA NA 179 TRUE +KIT2 KIT2.chr4.55592185.55592186 KIT2.chr4.55592185.55592186_tile_1 Homo sapiens hg19 chr4 55592185 55592186 - CAGTATGGTGTGATGCATGTATTACCA 0 CAGAAGTCTTGCCCACATCGTTGTAA 0 - ILLUMINA NA 188 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_1 Homo sapiens hg19 chr4 55593464 55593689 - GAGAGAACAAATAAATGGTTACCTGTAAA 0 GTGGAATCACAAACTTTGGCAGGA 0 - ILLUMINA NA 172 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_2 Homo sapiens hg19 chr4 55593464 55593689 + CGTAGCTGGCATGATGTGCATTATTG 0 ACCCATGTATGAAGTACAGTGGAAGG 0 + ILLUMINA NA 175 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_3 Homo sapiens hg19 chr4 55593464 55593689 - GTGACATGGAAAGCCCCTGTTTCATA 0 TCTGTGGGGAGAAAGGGAAAAATAGAT 0 - ILLUMINA NA 185 TRUE +KIT20_21 KIT20_21.chr4.55594221.55594258 KIT20_21.chr4.55594221.55594258_tile_1 Homo sapiens hg19 chr4 55594221 55594258 - GCAGTTTATAATCTAGCATTGCCAAAAT 0 AGTTCAGACATGAGGGCTTCCCGTTCT 0 - ILLUMINA NA 189 TRUE +KIT22 KIT22.chr4.55595519.55595519 KIT22.chr4.55595519.55595519_tile_1 Homo sapiens hg19 chr4 55595519 55595519 - ACTATTTATGTAAATCAGTCTTACCAGGA 0 TAATGACCAGGGTGGGCCCTAAAAGC 0 - ILLUMINA NA 184 TRUE +KIT23 KIT23.chr4.55597495.55597497 KIT23.chr4.55597495.55597497_tile_1 Homo sapiens hg19 chr4 55597495 55597497 - CCACATTAGCATGATATACATACTCTCT 0 CTGGGAGAGATGAAACAAGTCATGACT 0 - ILLUMINA NA 187 TRUE +KIT24_28 KIT24_28.chr4.55599320.55599348 KIT24_28.chr4.55599320.55599348_tile_1 Homo sapiens hg19 chr4 55599320 55599348 - TGTGTGATATCCCTAGACAGGATTTAC 0 GGCTAGACCAAAATCACAAATCTTTGT 0 - ILLUMINA NA 184 TRUE +KIT29 KIT29.chr4.55602694.55602694 KIT29.chr4.55602694.55602694_tile_1 Homo sapiens hg19 chr4 55602694 55602694 - GAAGCAGGACACCAATGAAACTTCAAG 0 TGCCATCCACTTCACAGGTAGTCGA 0 - ILLUMINA NA 186 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_1 Homo sapiens hg19 chr4 55946114 55946257 - ATTCTCCAGCCTGACTCGGGGACCACACTG 0 CATTTGATTTTCATTTCGACAACAGAAAAA 0 - ILLUMINA NA 173 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_2 Homo sapiens hg19 chr4 55946114 55946257 + ATGCTTCCTTTTAAACAGGAGGAGAGC 0 GGACTGGTAGCCGCTTGTCTGGTTTGA 0 + ILLUMINA NA 188 TRUE +KDR3 KDR3.chr4.55953807.55953807 KDR3.chr4.55953807.55953807_tile_1 Homo sapiens hg19 chr4 55953807 55953807 - CTGAAGCCATAACAACAGTCTTCTGTG 0 ATTCCATTATGACAACACAGCAGGAAT 0 - ILLUMINA NA 190 TRUE +KDR4 KDR4.chr4.55955111.55955127 KDR4.chr4.55955111.55955127_tile_1 Homo sapiens hg19 chr4 55955111 55955127 - TCCTTATTTAGCATCTCACCTCGTCAG 0 AGCCCAGTCAGAGACCCACGTTTT 0 - ILLUMINA NA 174 TRUE +KDR6 KDR6.chr4.55960989.55961023 KDR6.chr4.55960989.55961023_tile_1 Homo sapiens hg19 chr4 55960989 55961023 - TTTATAGACCAAAGGGGCACGATTCCG 0 TGTAGAAGAAGAGGAAGGTACTGGCTA 0 - ILLUMINA NA 172 TRUE +KDR8 KDR8.chr4.55962507.55962507 KDR8.chr4.55962507.55962507_tile_1 Homo sapiens hg19 chr4 55962507 55962507 - GGAAATGCATGTGGTCTGTAAACTAGG 0 AACACACAGTGAGCATCGAGCTCTCA 0 - ILLUMINA NA 178 TRUE +KDR9 KDR9.chr4.55972964.55972964 KDR9.chr4.55972964.55972964_tile_1 Homo sapiens hg19 chr4 55972964 55972964 - TACCATGGTAGGCTGCGTTGGAAGTTA 0 GACAAACCCATACCCTTGTGAAGAATG 0 - ILLUMINA NA 172 TRUE +KDR10 KDR10.chr4.55979623.55979623 KDR10.chr4.55979623.55979623_tile_1 Homo sapiens hg19 chr4 55979623 55979623 - CTGGTGTCCCTGTTTTTAGCATTAAAT 0 ACCTAAAAACCCAGTCTGGGAGTGAG 0 - ILLUMINA NA 182 TRUE +KDR11 KDR11.chr4.55980348.55980348 KDR11.chr4.55980348.55980348_tile_1 Homo sapiens hg19 chr4 55980348 55980348 - TCTGTGCAAAGTTATAGGCTTATTTGC 0 AGAACTGAACTAAATGTGGGGATTGAC 0 - ILLUMINA NA 178 TRUE +FBXW7_1 FBXW7_1.chr4.153245446.153245446 FBXW7_1.chr4.153245446.153245446_tile_1 Homo sapiens hg19 chr4 153245446 153245446 - CAGTAATTGATAGGAAGAGTATCCATACT 0 AACAAGTGGAATGGAACTCAAAGACAA 0 - ILLUMINA NA 190 TRUE +FBXW7_2 FBXW7_2.chr4.153247288.153247366 FBXW7_2.chr4.153247288.153247366_tile_1 Homo sapiens hg19 chr4 153247288 153247366 - GTTTTGTTTTGTTTTTCTGTTTCTCCCT 0 TATGATGGCAGGAGGGTTGTTAGTGGAGCA 0 - ILLUMINA NA 171 TRUE +FBXW7_5 FBXW7_5.chr4.153249384.153249384 FBXW7_5.chr4.153249384.153249384_tile_1 Homo sapiens hg19 chr4 153249384 153249384 - CATACAGGTGGAGTATGGTCATCACAA 0 AAAAGGTAAGGGAAAATCTTGTCATGG 0 - ILLUMINA NA 184 TRUE +FBXW7_7 FBXW7_7.chr4.153250883.153250883 FBXW7_7.chr4.153250883.153250883_tile_1 Homo sapiens hg19 chr4 153250883 153250883 - CTGTTCCTGTTTATGCCTTCATTTTTC 0 AGTTAGTGGTTCTGATGACAACACTT 0 - ILLUMINA NA 180 TRUE +FBXW7_8 FBXW7_8.chr4.153258983.153258983 FBXW7_8.chr4.153258983.153258983_tile_1 Homo sapiens hg19 chr4 153258983 153258983 - CTGTAATTTGGGACATCTGTTAAAACAATA 0 GACTTCATTTCATTGCTCCCTAAAGAGG 0 - ILLUMINA NA 191 TRUE +APC1 APC1.chr5.112173917.112173917 APC1.chr5.112173917.112173917_tile_1 Homo sapiens hg19 chr5 112173917 112173917 - GCAGAGCTTCTTCTAAGTGCATTTCTC 0 TGAAGAAGTTCCTGGATTTTCTGTTGC 0 - ILLUMINA NA 186 TRUE +APC2 APC2.chr5.112174631.112174631 APC2.chr5.112174631.112174631_tile_1 Homo sapiens hg19 chr5 112174631 112174631 - AATTTGTTGGTCTCTCTTCTTCTTCAT 0 TTTGTTTCTGAACCATTGGCTCCCCGT 0 - ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_1 Homo sapiens hg19 chr5 112175162 112175958 + CTTGCAAAGTTTCTTCTATTAACCAAGA 0 TTCTGCTAATACCCTGCAAATAGCAGA 0 + ILLUMINA NA 176 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_2 Homo sapiens hg19 chr5 112175162 112175958 - TGCTGGATTTGGTTCTAGGGTGCT 0 CCTATTTCATCTTCAGCTGATGACAAA 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_3 Homo sapiens hg19 chr5 112175162 112175958 + GAAAAGATTGGAACTAGGTCAGCTGAAG 0 AGCGAAATCTCCCTCCAAAAGTGGT 0 + ILLUMINA NA 172 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_4 Homo sapiens hg19 chr5 112175162 112175958 - CTATCAAGTGAACTGACAGAAGTACATC 0 CCTGGCTGATTCTGAAGATAAACTAGAACC 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_5 Homo sapiens hg19 chr5 112175162 112175958 + CACCCAAAAGTCCACCTGAACACTAT 0 ATTATAAGCCCCAGTGATCTTCCAGAT 0 + ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_6 Homo sapiens hg19 chr5 112175162 112175958 - CTCTCTCTTTTCAGCAGTAGGTGCTT 0 CACTTACCATTCCACTGCATGGTTCA 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_7 Homo sapiens hg19 chr5 112175162 112175958 + CAAACCAAGCGAGAAGTACCTAAAAAT 0 AAAGTACTCCAGATGGATTTTCTTGTTC 0 + ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_8 Homo sapiens hg19 chr5 112175162 112175958 - CTCTGATTCTGTTTCATTCCCATTGTCATT 0 GTGGCAAAATGTAATAAAGTATCAGCATCT 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_9 Homo sapiens hg19 chr5 112175162 112175958 + ATTAAGAATAATGCCTCCAGTTCAGGA 0 AGAAGAATGTATTATTTCTGCCATGCC 0 + ILLUMINA NA 190 TRUE +CSF1R1_3 CSF1R1_3.chr5.149433644.149433646 CSF1R1_3.chr5.149433644.149433646_tile_1 Homo sapiens hg19 chr5 149433644 149433646 - TCCCACCCTCAGGACTATACCAATCT 0 AGTTCTGCTGAGGAGTTGACGACAGGG 0 - ILLUMINA NA 185 TRUE +CSF1R4 CSF1R4.chr5.149453044.149453044 CSF1R4.chr5.149453044.149453044_tile_1 Homo sapiens hg19 chr5 149453044 149453044 - TCTTGGGTGGTGGGGACTATGTACCT 0 AACTTGAGCTCTGAGCAGAACCTCATC 0 - ILLUMINA NA 175 TRUE +NPM1 NPM1.chr5.170837547.170837548 NPM1.chr5.170837547.170837548_tile_1 Homo sapiens hg19 chr5 170837547 170837548 - GGTAGGGAAAGTTCTCACTCTGCATTA 0 AAAAAGAAATGTGGTTAAGGAACCAC 0 - ILLUMINA NA 186 TRUE +EGFR1 EGFR1.chr7.55211080.55211080 EGFR1.chr7.55211080.55211080_tile_1 Homo sapiens hg19 chr7 55211080 55211080 - CATCGGAACTGCTGTCTGCATTTATGA 0 GATGATCTGCAGGTTTTCCAAAGGAAT 0 - ILLUMINA NA 188 TRUE +EGFR2 EGFR2.chr7.55221822.55221822 EGFR2.chr7.55221822.55221822_tile_1 Homo sapiens hg19 chr7 55221822 55221822 - AAGCAAGGCAAACACATCCACCCAAAG 0 AAAGCTGTATTTGCCCTCGGGGTTCA 0 - ILLUMINA NA 174 TRUE +EGFR3 EGFR3.chr7.55233043.55233043 EGFR3.chr7.55233043.55233043_tile_1 Homo sapiens hg19 chr7 55233043 55233043 - AACTTGGGAGACATTTTTGATCTCTGA 0 TGCCGGGCAGGTCTTGACGCAGT 0 - ILLUMINA NA 186 TRUE +EGFR4 EGFR4.chr7.55241677.55241708 EGFR4.chr7.55241677.55241708_tile_1 Homo sapiens hg19 chr7 55241677 55241708 - GGAAATATACAGCTTGCAAGGACTCTG 0 TCAAGATCCTCAAGAGAGCTTGGTTG 0 - ILLUMINA NA 180 TRUE +EGFR9 EGFR9.chr7.55242418.55242511 EGFR9.chr7.55242418.55242511_tile_1 Homo sapiens hg19 chr7 55242418 55242511 - ATGAGAAAAGGTGGGCCTGAGGTTCAG 0 CCTATGACAGAGAGAGAAGGAAGACGTT 0 - ILLUMINA NA 190 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_1 Homo sapiens hg19 chr7 55249005 55249131 - AGGTGAGGCAGATGCCCAGCAGGCGG 0 CGCATGAATGCGATCTTGAGTTTCAA 0 - ILLUMINA NA 175 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_2 Homo sapiens hg19 chr7 55249005 55249131 + CAGCGTGGACAACCCCCACGTGT 0 GTGTGTGCAGATCGCAAAGGTAATCA 0 + ILLUMINA NA 177 TRUE +EGFR54 EGFR54.chr7.55259514.55259524 EGFR54.chr7.55259514.55259524_tile_1 Homo sapiens hg19 chr7 55259514 55259524 - CCTCCCCTGCATGTGTTAAACAATACA 0 CCAAAATCTGTGATCTTGACATGCTGC 0 - ILLUMINA NA 178 TRUE +MET1 MET1.chr7.116339642.116339642 MET1.chr7.116339642.116339642_tile_1 Homo sapiens hg19 chr7 116339642 116339642 - CCTTCTCACTGATATCGAATGCAATGG 0 CTTCTATCTGTGGGGAGAATATGCAGT 0 - ILLUMINA NA 180 TRUE +MET2 MET2.chr7.116340262.116340262 MET2.chr7.116340262.116340262_tile_1 Homo sapiens hg19 chr7 116340262 116340262 - GCCCTGGATATTCTTTTTGAGACTGAT 0 GAAGAAGTCGTTGACATATTTGATAGG 0 - ILLUMINA NA 188 TRUE +MET3 MET3.chr7.116411990.116411990 MET3.chr7.116411990.116411990_tile_1 Homo sapiens hg19 chr7 116411990 116411990 - TGCAAAACCAAAAATAAACAACAATGTC 0 TTACACTTCGGGCACTTACAAGCCTA 0 - ILLUMINA NA 171 TRUE +MET4 MET4.chr7.116417463.116417464 MET4.chr7.116417463.116417464_tile_1 Homo sapiens hg19 chr7 116417463 116417464 - CACAAGGGGAAAGTGTAAATCAACGTTT 0 CACAACCAAAATGCCCTGTGCAAAAGA 0 - ILLUMINA NA 191 TRUE +MET6 MET6.chr7.116423413.116423474 MET6.chr7.116423413.116423474_tile_1 Homo sapiens hg19 chr7 116423413 116423474 - GAGGAGAAACTCAGAGATAACCAATAC 0 TGTCTCTGGCAAGACCAAAATCAGCA 0 - ILLUMINA NA 172 TRUE +SMO1 SMO1.chr7.128845101.128845101 SMO1.chr7.128845101.128845101_tile_1 Homo sapiens hg19 chr7 128845101 128845101 - TGACCAGGGTGAAGAGCGTGCAGAG 0 AAGGGCACTTCGCACTGGCCTGAA 0 - ILLUMINA NA 186 TRUE +SMO2 SMO2.chr7.128846040.128846040 SMO2.chr7.128846040.128846040_tile_1 Homo sapiens hg19 chr7 128846040 128846040 - ATTGCCACAGTGAGGACAAAGGGGAGT 0 GTACACGATGACAAAGATGATGACGCA 0 - ILLUMINA NA 186 TRUE +SMO3 SMO3.chr7.128846374.128846374 SMO3.chr7.128846374.128846374_tile_1 Homo sapiens hg19 chr7 128846374 128846374 - TAGCTGGGGTTTCAGCATGGGGGCAGC 0 AAGCCCGCACGGTATCGGTAGTTCT 0 - ILLUMINA NA 190 TRUE +SMO4 SMO4.chr7.128850341.128850341 SMO4.chr7.128850341.128850341_tile_1 Homo sapiens hg19 chr7 128850341 128850341 - AACCACTGACCAAGGCTGTGCTAGAGG 0 TCATGGCGATGCCAGTTCCAAACA 0 - ILLUMINA NA 190 TRUE +SMO5 SMO5.chr7.128851593.128851593 SMO5.chr7.128851593.128851593_tile_1 Homo sapiens hg19 chr7 128851593 128851593 - TTCAGATCCTCTGGGGCCTTTCCTTC 0 AGAAATATCCTGGGGCAGTATGGCTCC 0 - ILLUMINA NA 173 TRUE +BRAF1 BRAF1.chr7.140453121.140453193 BRAF1.chr7.140453121.140453193_tile_1 Homo sapiens hg19 chr7 140453121 140453193 - ACCTAAACTCTTCATAATGCTTGCTCT 0 GGTCCCATCAGTTTGAACAGTTGTCT 0 - ILLUMINA NA 176 TRUE +BRAF28 BRAF28.chr7.140481397.140481478 BRAF28.chr7.140481397.140481478_tile_1 Homo sapiens hg19 chr7 140481397 140481478 - GGTTTTCTTTTTCTGTTTGGCTTGACT 0 CTACAAGGGAAAGTGGCATGGTAAGTA 0 - ILLUMINA NA 178 TRUE +FGFR1_1 FGFR1_1.chr8.38282209.38282209 FGFR1_1.chr8.38282209.38282209_tile_1 Homo sapiens hg19 chr8 38282209 38282209 - TTTTGAGAGGCTTGGGCTCAGCAGAA 0 TCACCGGCCCATCCTGCAAGCAGGG 0 - ILLUMINA NA 179 TRUE +FGFR1_2 FGFR1_2.chr8.38285938.38285938 FGFR1_2.chr8.38285938.38285938_tile_1 Homo sapiens hg19 chr8 38285938 38285938 - AAGAGATCATCACTAAGGGAGCAGTGG 0 GGATGATGATGATGATGATGACTCCTC 0 - ILLUMINA NA 184 TRUE +JAK2_1 JAK2_1.chr9.5073769.5073770 JAK2_1.chr9.5073769.5073770_tile_1 Homo sapiens hg19 chr9 5073769 5073770 - TTCAGTTTCAAAAATACTTAACTCCTGTT 0 CTCCATAATTTAAAACCAAATGCTTGTG 0 - ILLUMINA NA 188 TRUE +CDKN2A1 CDKN2A1.chr9.21971153.21971187 CDKN2A1.chr9.21971153.21971187_tile_1 Homo sapiens hg19 chr9 21971153 21971187 - TTGTGTGGGGGTCTGCTTGGCGGTGA 0 AACTGCGCCGACCCCGCCACTCTCA 0 - ILLUMINA NA 187 TRUE +ABL1_1 ABL1_1.chr9.133738330.133738364 ABL1_1.chr9.133738330.133738364_tile_1 Homo sapiens hg19 chr9 133738330 133738364 - ATGCATCGCCTAATGCCAGCAGACGC 0 TGATGTCCGTGCGTTCCATCTCCCAC 0 - ILLUMINA NA 191 TRUE +ABL1_9 ABL1_9.chr9.133747520.133747520 ABL1_9.chr9.133747520.133747520_tile_1 Homo sapiens hg19 chr9 133747520 133747520 - AGCGCCTGTGTCACCCTGGGGGT 0 AAAACGAAGGTGAAATTATTTCAGGAA 0 - ILLUMINA NA 190 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_1 Homo sapiens hg19 chr9 133748283 133748414 + AGAATCCTTCAGAAGGCTTTTTCTTTAGAC 0 AACCTCCTGGACTACCTGAGGGAGT 0 + ILLUMINA NA 172 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_2 Homo sapiens hg19 chr9 133748283 133748414 - TCCATGGCGCAGGCTGCCTGGCC 0 CCGTAGGTCATGAACTCAGTGATGA 0 - ILLUMINA NA 182 TRUE +ABL1_16 ABL1_16.chr9.133750356.133750356 ABL1_16.chr9.133750356.133750356_tile_1 Homo sapiens hg19 chr9 133750356 133750356 - GGGAAGAGCAAGAAAGAGGCAGAAAAA 0 TGTGTAGGTGTCCCCTGTCATCAA 0 - ILLUMINA NA 190 TRUE +NOTCH1_1 NOTCH1_1.chr9.139397768.139397768 NOTCH1_1.chr9.139397768.139397768_tile_1 Homo sapiens hg19 chr9 139397768 139397768 - AGACCTGGCTTCCCACCACCCCAGGCT 0 AGATTGACAACCGGCAGTGTGTGCAG 0 - ILLUMINA NA 190 TRUE +NOTCH1_2 NOTCH1_2.chr9.139399344.139399422 NOTCH1_2.chr9.139399344.139399422_tile_1 Homo sapiens hg19 chr9 139399344 139399422 - AGTGCGAGTGGGACGGGCTGGACTGT 0 ACACCAACGTGGTCTTCAAGCGTGAC 0 - ILLUMINA NA 171 TRUE +RET1 RET1.chr10.43609078.43609104 RET1.chr10.43609078.43609104_tile_1 Homo sapiens hg19 chr10 43609078 43609104 - ACTCGCCTCCCAGCAATTTCCTCCC 0 TTGCAGGTGCCATAGCCAGCTTTAAT 0 - ILLUMINA NA 180 TRUE +RET2_9 RET2_9.chr10.43609940.43609950 RET2_9.chr10.43609940.43609950_tile_1 Homo sapiens hg19 chr10 43609940 43609950 + AAGCCTCACACCACCCCCACCCACAGAT 0 CCCATCTCCTCAGCTGAGATGACCTT 0 + ILLUMINA NA 175 TRUE +RET10 RET10.chr10.43613840.43613840 RET10.chr10.43613840.43613840_tile_1 Homo sapiens hg19 chr10 43613840 43613840 - AGAACAGGGCTGTATGGAGCCCCCAGC 0 GGGAGGCGTTCTCTGAAATGCAG 0 - ILLUMINA NA 190 TRUE +RET11_12 RET11_12.chr10.43615567.43615569 RET11_12.chr10.43615567.43615569_tile_1 Homo sapiens hg19 chr10 43615567 43615569 - ATGGTGCACCTGGGATCCCTGGGAG 0 ATGTTTCTGGCTGCCAAGTCCCGATGAA 0 - ILLUMINA NA 172 TRUE +RET13 RET13.chr10.43617416.43617416 RET13.chr10.43617416.43617416_tile_1 Homo sapiens hg19 chr10 43617416 43617416 - AATTCCCTGGCCAAGCTGCACAGACGG 0 CCATTTAACTGGAATCCGACCCTAAAG 0 - ILLUMINA NA 178 TRUE +PTEN1 PTEN1.chr10.89624242.89624244 PTEN1.chr10.89624242.89624244_tile_1 Homo sapiens hg19 chr10 89624242 89624244 - TACGGACATTTTCGCATCCGTCTACTC 0 ATGATGGCTGTCATGTCTGGGAGCCTG 0 - ILLUMINA NA 176 TRUE +PTEN3 PTEN3.chr10.89685307.89685307 PTEN3.chr10.89685307.89685307_tile_1 Homo sapiens hg19 chr10 89685307 89685307 - TGGACTTCTTGACTTAATCGGTTTAGG 0 CTTGTAATGGTTTTTATGCTTTGAATCCA 0 - ILLUMINA NA 186 TRUE +PTEN4 PTEN4.chr10.89711893.89711900 PTEN4.chr10.89711893.89711900_tile_1 Homo sapiens hg19 chr10 89711893 89711900 - GGATGAGAATTTCAAGCACTTACTGCA 0 TGGGAATAGTTACTCCCTGGTGGACA 0 - ILLUMINA NA 176 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_1 Homo sapiens hg19 chr10 89717615 89717772 - GGGTCCTGAATTGGAGGAATATATCTTCAC 0 ACACGAAATATGGATTCTGTATCTGC 0 - ILLUMINA NA 181 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_2 Homo sapiens hg19 chr10 89717615 89717772 + CAGTTTGTGGTCTGCCAGCTAAA 0 AAAGGTTTGTACTTTACTTTCATTGGGAG 0 + ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_1 Homo sapiens hg19 chr10 89720716 89720852 - AATTTGGAGAAAAGTATCGGTTGGCTT 0 AGGTTTCCTCTGGTCCTGGTATGAA 0 - ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_2 Homo sapiens hg19 chr10 89720716 89720852 + AAAATGATCTTGACAAAGCAAATAAAGAC 0 CTTGCTTGACAAGTTTTTAACTTATGTATT 0 + ILLUMINA NA 179 TRUE +FGFR2_1 FGFR2_1.chr10.123258034.123258034 FGFR2_1.chr10.123258034.123258034_tile_1 Homo sapiens hg19 chr10 123258034 123258034 - CTAACAGTAGCTGCCCATGAGTTAGAG 0 TTCTTGGAGCCTGCACACAGGATGGTG 0 - ILLUMINA NA 180 TRUE +FGFR2_2 FGFR2_2.chr10.123274774.123274803 FGFR2_2.chr10.123274774.123274803_tile_1 Homo sapiens hg19 chr10 123274774 123274803 - GCCTTTTGGTTCCTTTGGTTGTGCTAT 0 CATAGGGGTCTTCTTAATCGCCTGTAT 0 - ILLUMINA NA 186 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_1 Homo sapiens hg19 chr10 123279503 123279677 - CACGTGGAAAAGAACGGCAGTAAATAC 0 GGAGTTGAGAGAGGATGATTCTCTTTT 0 - ILLUMINA NA 172 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_2 Homo sapiens hg19 chr10 123279503 123279677 + TTTAGATTCAGAAAGTCCTCACCTTGAG 0 CTCCTCCGACCACTGTGGAGGCATTT 0 + ILLUMINA NA 171 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_3 Homo sapiens hg19 chr10 123279503 123279677 - ACTGACAGCCCTCTGGACAACACAGCT 0 CGTAGAGTTTGTCTGCAAGGTTTACAG 0 - ILLUMINA NA 184 TRUE +HRAS1 HRAS1.chr11.533873.533875 HRAS1.chr11.533873.533875_tile_1 Homo sapiens hg19 chr11 533873 533875 - TACCAGGGAGAGGCTGGCTGTGTGAAC 0 AGTACAGCGCCATGCGGGACCAGTAC 0 - ILLUMINA NA 180 TRUE +HRAS6 HRAS6.chr11.534285.534289 HRAS6.chr11.534285.534289_tile_1 Homo sapiens hg19 chr11 534285 534289 - CTGCCCTGTGGGGCCTGGGGCTGG 0 AAGAGTGCGCTGACCATCCAGCTGATC 0 - ILLUMINA NA 185 TRUE +ATM1 ATM1.chr11.108117847.108117848 ATM1.chr11.108117847.108117848_tile_1 Homo sapiens hg19 chr11 108117847 108117848 - GAAAGGAATAGTTGCATGTACAGAGTC 0 GATATCTGCCATCAATTCAATCAAATTTT 0 - ILLUMINA NA 174 TRUE +ATM2 ATM2.chr11.108119823.108119823 ATM2.chr11.108119823.108119823_tile_1 Homo sapiens hg19 chr11 108119823 108119823 - TTGCTAGTAATAGGTTTGGGGGTAGAC 0 GATCAAAATCATTCTGTGACTTCTGAA 0 - ILLUMINA NA 172 TRUE +ATM3 ATM3.chr11.108123551.108123551 ATM3.chr11.108123551.108123551_tile_1 Homo sapiens hg19 chr11 108123551 108123551 - AAGCTATAGCTTAAAATGATAAAGAGCAT 0 ACAAAGAAAAACAAAAAGCTTCACTTAGA 0 - ILLUMINA NA 172 TRUE +ATM4 ATM4.chr11.108137973.108138003 ATM4.chr11.108137973.108138003_tile_1 Homo sapiens hg19 chr11 108137973 108138003 - ACTGCCAAATCAATATAAAGAAGTAAAAGA 0 GATTTCCATTAGTATCATCTTCCATTGAT 0 - ILLUMINA NA 189 TRUE +ATM6 ATM6.chr11.108155132.108155132 ATM6.chr11.108155132.108155132_tile_1 Homo sapiens hg19 chr11 108155132 108155132 - TCGAATAAATAGCCTTAAAACTTAAAGGTT 0 ATCCCACTGTCTCTGGTACCCTCATAG 0 - ILLUMINA NA 179 TRUE +ATM7 ATM7.chr11.108170476.108170479 ATM7.chr11.108170476.108170479_tile_1 Homo sapiens hg19 chr11 108170476 108170479 - ACTCACCAATCTTCTACCAGTGTGTTA 0 ACTTCTCCCAAGCAGCTTCCAACAGCC 0 - ILLUMINA NA 178 TRUE +ATM9 ATM9.chr11.108172421.108172421 ATM9.chr11.108172421.108172421_tile_1 Homo sapiens hg19 chr11 108172421 108172421 - ACAGAACTGTTTTAGATATGCTGGGTA 0 AATGTTTTTCAAACAGGTAACAGCTGC 0 - ILLUMINA NA 182 TRUE +ATM10 ATM10.chr11.108173640.108173640 ATM10.chr11.108173640.108173640_tile_1 Homo sapiens hg19 chr11 108173640 108173640 - CAGGTCATAAACAAGGAATTATATCAGACT 0 ATATCATCCAGGCCTTCAAAAGGG 0 - ILLUMINA NA 191 TRUE +ATM11 ATM11.chr11.108180945.108180945 ATM11.chr11.108180945.108180945_tile_1 Homo sapiens hg19 chr11 108180945 108180945 - CCCTTATTGAGACAATGCCAACATTAA 0 CTAGATAATTTAAATCCAGCCAGAAAGC 0 - ILLUMINA NA 188 TRUE +ATM12 ATM12.chr11.108200958.108200961 ATM12.chr11.108200958.108200961_tile_1 Homo sapiens hg19 chr11 108200958 108200961 - CAAAGTCGGAATACCCACATATCATGT 0 CCTTTACTGTGTATCTTGCATAGAATAAT 0 - ILLUMINA NA 172 TRUE +ATM14 ATM14.chr11.108204681.108204681 ATM14.chr11.108204681.108204681_tile_1 Homo sapiens hg19 chr11 108204681 108204681 - TAGGTTGAAACATATGAAATTTGCCAA 0 GGGACAACAACATCTTCTAAATTCTTAAG 0 - ILLUMINA NA 174 TRUE +ATM15 ATM15.chr11.108205769.108205769 ATM15.chr11.108205769.108205769_tile_1 Homo sapiens hg19 chr11 108205769 108205769 - GACAAAATCCCAAATAAAGCAGAAAGAA 0 CCTGCTAAGCGAAATTCTGCTTTAAATG 0 - ILLUMINA NA 191 TRUE +ATM16 ATM16.chr11.108206594.108206594 ATM16.chr11.108206594.108206594_tile_1 Homo sapiens hg19 chr11 108206594 108206594 - CACCCAACCAAATGGCATCTTTTATAT 0 TTGTCTCAGGTCATCACGGCCCTTCAG 0 - ILLUMINA NA 186 TRUE +ATM17 ATM17.chr11.108218089.108218089 ATM17.chr11.108218089.108218089_tile_1 Homo sapiens hg19 chr11 108218089 108218089 - CTAGGACAACTGTTTATGCTGAAAACA 0 TCTATATGTACAAGTTCTGCTGACTGC 0 - ILLUMINA NA 188 TRUE +ATM18 ATM18.chr11.108225590.108225590 ATM18.chr11.108225590.108225590_tile_1 Homo sapiens hg19 chr11 108225590 108225590 - GCTAAGTGCACAATCTCCTCCTTTCT 0 AACAGAGTTTCCTGAGAGTTTCTCATC 0 - ILLUMINA NA 191 TRUE +ATM19 ATM19.chr11.108236086.108236203 ATM19.chr11.108236086.108236203_tile_1 Homo sapiens hg19 chr11 108236086 108236203 - TGAAGATCACACCCAAGCTTTCCATC 0 TCAGCTACTTTGTTGAAACTCTGGTCA 0 - ILLUMINA NA 185 TRUE +KRAS1 KRAS1.chr12.25378562.25378562 KRAS1.chr12.25378562.25378562_tile_1 Homo sapiens hg19 chr12 25378562 25378562 - TCTTTCCCAGAGAACAAATTAAAAGAGT 0 AGACAAGACAGGTAAGTAACACTGAAA 0 - ILLUMINA NA 187 TRUE +KRAS2 KRAS2.chr12.25380275.25380283 KRAS2.chr12.25380275.25380283_tile_1 Homo sapiens hg19 chr12 25380275 25380283 - TTGTTGTTGAGTTGTATATAACACCTTTT 0 AGTACAGTGCAATGAGGGACCAGTAC 0 - ILLUMINA NA 184 TRUE +KRAS7 KRAS7.chr12.25398255.25398285 KRAS7.chr12.25398255.25398285_tile_1 Homo sapiens hg19 chr12 25398255 25398285 - GGTACTGGTGGAGTATTTGATAGTGTAT 0 GCTAATTCAGAATCATTTTGTGGACGAAT 0 - ILLUMINA NA 191 TRUE +PTPN11_1 PTPN11_1.chr12.112888163.112888211 PTPN11_1.chr12.112888163.112888211_tile_1 Homo sapiens hg19 chr12 112888163 112888211 - TACTGACCTTTCAGAGGTAGGATCTGC 0 GTGTTCTGAATCTTGATGTGGGTGAC 0 - ILLUMINA NA 190 TRUE +PTPN11_10 PTPN11_10.chr12.112926884.112926888 PTPN11_10.chr12.112926884.112926888_tile_1 Homo sapiens hg19 chr12 112926884 112926888 - CAAGAGGCCTAGCAAGAGAATGAGAAT 0 TCTGAGACCGCACCATCTGGATGGTT 0 - ILLUMINA NA 178 TRUE +HNF1A_1 HNF1A_1.chr12.121431413.121431414 HNF1A_1.chr12.121431413.121431414_tile_1 Homo sapiens hg19 chr12 121431413 121431414 - TTGCCGCAGCCCAGACCAAACCAGCA 0 TTGAAACGGTTCCTCCGCCCCTTCTT 0 - ILLUMINA NA 175 TRUE +HNF1A_3 HNF1A_3.chr12.121432070.121432070 HNF1A_3.chr12.121432070.121432070_tile_1 Homo sapiens hg19 chr12 121432070 121432070 - ACATACCACTTACCGTGGACCTTACT 0 CGGTTGGCAAACCAGTTGTAGACA 0 - ILLUMINA NA 181 TRUE +FLT3_1 FLT3_1.chr13.28592620.28592653 FLT3_1.chr13.28592620.28592653_tile_1 Homo sapiens hg19 chr13 28592620 28592653 - CACATCACAGTAAATAACACTCTGGTG 0 TTGTCAGGGGCAATGTGAGGCTGCTATT 0 - ILLUMINA NA 178 TRUE +FLT3_13 FLT3_13.chr13.28602329.28602329 FLT3_13.chr13.28602329.28602329_tile_1 Homo sapiens hg19 chr13 28602329 28602329 - ACTTGAGTTTTACATTTTTAATGCTCCT 0 TGTCAGGTAACCCACTTCCACGAAAA 0 - ILLUMINA NA 171 TRUE +FLT3_14 FLT3_14.chr13.28608244.28608341 FLT3_14.chr13.28608244.28608341_tile_1 Homo sapiens hg19 chr13 28608244 28608341 - CTATCTGCAGAACTGCCTATTCCTAAC 0 TTCCAAGAGAAAATTTAGAGTTTGGTAAG 0 - ILLUMINA NA 190 TRUE +FLT3_22 FLT3_22.chr13.28610138.28610138 FLT3_22.chr13.28610138.28610138_tile_1 Homo sapiens hg19 chr13 28610138 28610138 + CCAGGTCCAAGATGGTAATGGGTAT 0 ATACCAATACTTTGTGAAGCCAAGGTGG 0 + ILLUMINA NA 171 TRUE +RB1_1 RB1_1.chr13.48919244.48919244 RB1_1.chr13.48919244.48919244_tile_1 Homo sapiens hg19 chr13 48919244 48919244 - CCTTTCCAATTTGCTGAAGAGTGCAAA 0 CAGTAACCTTAAAAATTTGTGTTATTTCGT 0 - ILLUMINA NA 182 TRUE +RB1_2 RB1_2.chr13.48923148.48923148 RB1_2.chr13.48923148.48923148_tile_1 Homo sapiens hg19 chr13 48923148 48923148 - GCTAACAGTTAATAAGCCAAGCAGAGA 0 AAATGTGATCCAAGAAACTTTTAGCAC 0 - ILLUMINA NA 178 TRUE +RB1_3 RB1_3.chr13.48942685.48942685 RB1_3.chr13.48942685.48942685_tile_1 Homo sapiens hg19 chr13 48942685 48942685 - ACATAAAGAAACGTGAACAAATCTGAAA 0 GGTGTTCTCTGTGTTTCAAAACTAAATAA 0 - ILLUMINA NA 173 TRUE +RB1_4 RB1_4.chr13.48955538.48955550 RB1_4.chr13.48955538.48955550_tile_1 Homo sapiens hg19 chr13 48955538 48955550 - TTCCCTATATGTTCTTGAGGTAGATGT 0 AATGTTTTATCATTTCTCTTGTCAAGTTG 0 - ILLUMINA NA 182 TRUE +RB1_6 RB1_6.chr13.49027168.49027168 RB1_6.chr13.49027168.49027168_tile_1 Homo sapiens hg19 chr13 49027168 49027168 - TTTGCAGTTTGAATGGTCAACATAACA 0 TAAAGGTGAATCCTATATGAAACATGATG 0 - ILLUMINA NA 178 TRUE +RB1_7 RB1_7.chr13.49033843.49033846 RB1_7.chr13.49033843.49033846_tile_1 Homo sapiens hg19 chr13 49033843 49033846 - GAAGTGCTTGATTTTCTTACTTGGTCC 0 TAGGCTAGCCGATACACTGTGGGAATA 0 - ILLUMINA NA 178 TRUE +RB1_8 RB1_8.chr13.49037877.49037877 RB1_8.chr13.49037877.49037877_tile_1 Homo sapiens hg19 chr13 49037877 49037877 - GGAAAATTACCTACCTCCTGAACAGCA 0 AGTAGTCAGAATTTTATTACATGGTTTTGT 0 - ILLUMINA NA 172 TRUE +RB1_9 RB1_9.chr13.49039164.49039164 RB1_9.chr13.49039164.49039164_tile_1 Homo sapiens hg19 chr13 49039164 49039164 - TGTTTTGGTGGACCCATTACATTAGAT 0 CTTTGATCAAAACACGTTTGAATGTCT 0 - ILLUMINA NA 174 TRUE +AKT1 AKT1.chr14.105246455.105246455 AKT1.chr14.105246455.105246455_tile_1 Homo sapiens hg19 chr14 105246455 105246455 - TCTGACGGGTAGAGTGTGCGTGGCTC 0 GCTCCCCTCAACAACTTCTCTGTG 0 - ILLUMINA NA 173 TRUE +CDH1_1 CDH1_1.chr16.68835649.68835650 CDH1_1.chr16.68835649.68835650_tile_1 Homo sapiens hg19 chr16 68835649 68835650 - GGCGGTGGTGGTGCCCCACTGT 0 CTTTGAATCGGGTGTCGAGGGAAAAA 0 - ILLUMINA NA 171 TRUE +CDH1_2 CDH1_2.chr16.68846137.68846137 CDH1_2.chr16.68846137.68846137_tile_1 Homo sapiens hg19 chr16 68846137 68846137 - ACATTCTCTAGTCTGGAGAGAGTTTTC 0 TTGGTGTCAGTGACTGTGATCACAGCT 0 - ILLUMINA NA 176 TRUE +CDH1_3 CDH1_3.chr16.68847274.68847277 CDH1_3.chr16.68847274.68847277_tile_1 Homo sapiens hg19 chr16 68847274 68847277 - CATCTTGCCAGGTACCATACAAACCTT 0 CACTTTCAGTGTGGTGATTACGACGTT 0 - ILLUMINA NA 178 TRUE +TP53_1 TP53_1.chr17.7574003.7574021 TP53_1.chr17.7574003.7574021_tile_1 Homo sapiens hg19 chr17 7574003 7574021 - ACTAAATGCATGTTGCTTTTGTACCGT 0 AGAGCTGAATGAGGCCTTGGAACTC 0 - ILLUMINA NA 172 TRUE +TP53_3 TP53_3.chr17.7577022.7577129 TP53_3.chr17.7577022.7577129_tile_1 Homo sapiens hg19 chr17 7577022 7577129 - ATCCTGAGTAGTGGTAATCTACTGGGA 0 AGGTAAGCAAGCAGGACAAGAAGCG 0 - ILLUMINA NA 172 TRUE +TP53_17 TP53_17.chr17.7577523.7577574 TP53_17.chr17.7577523.7577574_tile_1 Homo sapiens hg19 chr17 7577523 7577574 - AAAAAGGCCTCCCCTGCTTGCCACAGG 0 ATCATCACACTGGAAGACTCCAGGTCA 0 - ILLUMINA NA 190 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_1 Homo sapiens hg19 chr17 7578190 7578536 - TTTGGATGACAGAAACACTTTTCGACA 0 CCTGCTGCTTATTTGACCTCCCTATAAC 0 - ILLUMINA NA 172 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_2 Homo sapiens hg19 chr17 7578190 7578536 + GACCCCAGTTGCAAACCAGACCTCA 0 TGAGGAATCAGAGGCCTGGGGA 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_3 Homo sapiens hg19 chr17 7578190 7578536 - TTGTGAGGCGCTGCCCCCACCATGAG 0 GCATCTTATCCGAGTGGAAGGAAATTTG 0 - ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_4 Homo sapiens hg19 chr17 7578190 7578536 + CGTCTCTCCAGCCCCAGCTGCTCACCAT 0 CCACAGCTGCACAGGGCAGGTCTT 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_5 Homo sapiens hg19 chr17 7578190 7578536 - GCATGTTTGTTTCTTTGCTGCCGTCT 0 TTGATTCCACACCCCCGCCCGGC 0 - ILLUMINA NA 179 TRUE +TP53_60 TP53_60.chr17.7579358.7579403 TP53_60.chr17.7579358.7579403_tile_1 Homo sapiens hg19 chr17 7579358 7579403 - AGATGAAGCTCCCAGAATGCCAGAGG 0 TTCTTGCATTCTGGGACAGCCAAGTCT 0 - ILLUMINA NA 185 TRUE +TP53_64 TP53_64.chr17.7579882.7579882 TP53_64.chr17.7579882.7579882_tile_1 Homo sapiens hg19 chr17 7579882 7579882 - ATGGTGTTGGGGGAGGGGGTTCCTTCT 0 CCCCTCTGAGTCAGGAAACATTTTCAG 0 - ILLUMINA NA 182 TRUE +ERBB2_1 ERBB2_1.chr17.37880219.37880261 ERBB2_1.chr17.37880219.37880261_tile_1 Homo sapiens hg19 chr17 37880219 37880261 - CATATCTCCCCAAACCCCAATGAAGAG 0 CTTTGATGGCCACTGGAATTTTCACA 0 - ILLUMINA NA 172 TRUE +ERBB2_4 ERBB2_4.chr17.37880993.37881012 ERBB2_4.chr17.37880993.37881012_tile_1 Homo sapiens hg19 chr17 37880993 37881012 - ATACACCAGTTCAGCAGGTCCTGGGAG 0 TATGCTTCCTGGGGACAAGGGTAC 0 - ILLUMINA NA 190 TRUE +ERBB2_13 ERBB2_13.chr17.37881332.37881440 ERBB2_13.chr17.37881332.37881440_tile_1 Homo sapiens hg19 chr17 37881332 37881440 - TCTGCTCCTTGGTCCTTCACCTAACCT 0 ACATCCTCCAGGTAGCTCATCCCCTGG 0 - ILLUMINA NA 186 TRUE +SMAD4_1 SMAD4_1.chr18.48575169.48575170 SMAD4_1.chr18.48575169.48575170_tile_1 Homo sapiens hg19 chr18 48575169 48575170 - TACAAAAATTGAAACACTATTGAGATCCT 0 CGCATACTGACAATATTTAACATGTTTTAG 0 - ILLUMINA NA 172 TRUE +SMAD4_2 SMAD4_2.chr18.48581198.48581198 SMAD4_2.chr18.48581198.48581198_tile_1 Homo sapiens hg19 chr18 48581198 48581198 - ATGTTGGGAAAGTTGGCAGTGCTGGTA 0 CAAAGTCATGCACATATTCATCCTTCAC 0 - ILLUMINA NA 180 TRUE +SMAD4_3 SMAD4_3.chr18.48584560.48584560 SMAD4_3.chr18.48584560.48584560_tile_1 Homo sapiens hg19 chr18 48584560 48584560 - GCTGTCTAAAAATTAAGGCCCACATGG 0 TGATGCTATCTGCAACAGTCCTTCAC 0 - ILLUMINA NA 188 TRUE +SMAD4_4 SMAD4_4.chr18.48586262.48586262 SMAD4_4.chr18.48586262.48586262_tile_1 Homo sapiens hg19 chr18 48586262 48586262 - ACTCATGTCATGATGAGTATTGTACTC 0 AATGCAAGCTCATTGTGAACAGGCCCT 0 - ILLUMINA NA 184 TRUE +SMAD4_5 SMAD4_5.chr18.48591826.48591919 SMAD4_5.chr18.48591826.48591919_tile_1 Homo sapiens hg19 chr18 48591826 48591919 - CAATACCTTGCTCTCTCAATGGCTTCT 0 AGTAAGCAATGGAACACCAATACTCAG 0 - ILLUMINA NA 188 TRUE +SMAD4_11 SMAD4_11.chr18.48593405.48593405 SMAD4_11.chr18.48593405.48593405_tile_1 Homo sapiens hg19 chr18 48593405 48593405 - GCACTTGGGTAGATCTTATGAACAGCA 0 TGCCTATGTGCAACCTTAGGAAGAAA 0 - ILLUMINA NA 172 TRUE +SMAD4_12 SMAD4_12.chr18.48603032.48603094 SMAD4_12.chr18.48603032.48603094_tile_1 Homo sapiens hg19 chr18 48603032 48603094 - AAAGAATGAAAAGCATACTTACTGATAGC 0 CTGACGCAAATCAAAGACCTTTTAAGAA 0 - ILLUMINA NA 172 TRUE +SMAD4_15 SMAD4_15.chr18.48604668.48604754 SMAD4_15.chr18.48604668.48604754_tile_1 Homo sapiens hg19 chr18 48604668 48604754 - GCATGGTATGAAGTACTTCGTCTAGGA 0 AAGGTCATCAACACCAATTCCAGCAG 0 - ILLUMINA NA 172 TRUE +STK11_1 STK11_1.chr19.1207021.1207092 STK11_1.chr19.1207021.1207092_tile_1 Homo sapiens hg19 chr19 1207021 1207092 - CGCAACTTCTTCTTCTTGAGGATCTTG 0 TAGATGACCTCGGTGGAGTCGATGCGG 0 - ILLUMINA NA 178 TRUE +STK11_4 STK11_4.chr19.1220487.1220502 STK11_4.chr19.1220487.1220502_tile_1 Homo sapiens hg19 chr19 1220487 1220502 - AAAGCCGGGGAGCCCTGGCTGGTC 0 AGATTTTGAGGGTGCCACCGGTGGTG 0 - ILLUMINA NA 181 TRUE +STK11_8 STK11_8.chr19.1221264.1221319 STK11_8.chr19.1221264.1221319_tile_1 Homo sapiens hg19 chr19 1221264 1221319 + TGTACCCCTTCGAAGGGGACAACATCTA 0 GCTTTTGTGCAGAAATGTAGGGTTGG 0 + ILLUMINA NA 177 TRUE +STK11_12 STK11_12.chr19.1223059.1223125 STK11_12.chr19.1223059.1223125_tile_1 Homo sapiens hg19 chr19 1223059 1223125 - ACATCCTGGCCGAGTCAGCAGAGCC 0 ACCGGTCCTTGGTGTCTGGGCTC 0 - ILLUMINA NA 188 TRUE +JAK3_1 JAK3_1.chr19.17945696.17945696 JAK3_1.chr19.17945696.17945696_tile_1 Homo sapiens hg19 chr19 17945696 17945696 - ATCCCTGATCCCACTTTCATTCCCTCA 0 ATGCCCATCAGTGCCCTGGATCCTG 0 - ILLUMINA NA 176 TRUE +JAK3_2 JAK3_2.chr19.17948009.17948009 JAK3_2.chr19.17948009.17948009_tile_1 Homo sapiens hg19 chr19 17948009 17948009 - TAGTGCTGTGTGCACTAATGGCAGACT 0 AGCTTGATGAGCCAAGTGTCGTAC 0 - ILLUMINA NA 190 TRUE +SRC SRC.chr20.36031762.36031762 SRC.chr20.36031762.36031762_tile_1 Homo sapiens hg19 chr20 36031762 36031762 - AAAGAGGAAGGGCCTCGCCCCTGGCAAT 0 TACTGGGGCTCGGTGGACGTGAAGTAG 0 - ILLUMINA NA 191 TRUE +GNAS1 GNAS1.chr20.57484420.57484421 GNAS1.chr20.57484420.57484421_tile_1 Homo sapiens hg19 chr20 57484420 57484421 - ACAGCTGGTTATTCCAGAGGGACTGGG 0 GCGAAGCAGGTCCTGAAACAAAATTGA 0 - ILLUMINA NA 172 TRUE +SMARCB1_1 SMARCB1_1.chr22.24133967.24133990 SMARCB1_1.chr22.24133967.24133990_tile_1 Homo sapiens hg19 chr22 24133967 24133990 - GCGAGTGGTTTTGAAACAGGTTTACA 0 ACATACGGAGGTAGTTTCCCACCTAT 0 - ILLUMINA NA 189 TRUE +SMARCB1_3 SMARCB1_3.chr22.24143240.24143240 SMARCB1_3.chr22.24143240.24143240_tile_1 Homo sapiens hg19 chr22 24143240 24143240 - TTGTGGGGAGCACAAGGTCAAAGCAG 0 ATGCGGTTCCTGTTGATGGTTGTGGA 0 - ILLUMINA NA 175 TRUE +SMARCB1_4 SMARCB1_4.chr22.24145582.24145582 SMARCB1_4.chr22.24145582.24145582_tile_1 Homo sapiens hg19 chr22 24145582 24145582 - ATGTCCTGCGTGTCAGGTCCAGAATCT 0 TTCTGCCCATCGATCTCCATGTCCAG 0 - ILLUMINA NA 176 TRUE +SMARCB1_5_6 SMARCB1_5_6.chr22.24176352.24176357 SMARCB1_5_6.chr22.24176352.24176357_tile_1 Homo sapiens hg19 chr22 24176352 24176357 - ACTCCACCCCCACCCGATCCTCAGGA 0 TGTTGGCAAGACGCCTCATCCGCCTGG 0 - ILLUMINA NA 173 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_1 Homo sapiens hg19 chr19 3114942 3115070 + AGTGCGCGGTCCACCCCCTCCT 0 CTGCCCACCCAGCAGGACGTGCT 0 + ILLUMINA NA 182 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_2 Homo sapiens hg19 chr19 3114942 3115070 - CGGCACACCGGGCAAATGAGCC 0 TAGCCCAAGGTGGCGATGCGGTC 0 - ILLUMINA NA 177 TRUE +GNA11_5 GNA11_5.chr19.3118922.3119051 GNA11_5.chr19.3118922.3119051_tile_1 Homo sapiens hg19 chr19 3118922 3119051 + TCCTGCTCCAGCCGATGTCAGTCT 0 GATCCACTGCTTTGAGAACGTGACAT 0 + ILLUMINA NA 189 TRUE +GNA11_6 GNA11_6.chr19.3119204.3119357 GNA11_6.chr19.3119204.3119357_tile_2 Homo sapiens hg19 chr19 3119204 3119357 + GGATGGAGGAGAGCAAAGCCCTGTT 0 CATGGGGAGGGGCTCGCGGGCA 0 + ILLUMINA NA 189 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_1 Homo sapiens hg19 chr19 3120987 3121177 - AACATCTTCAGGATGAACTCCCGCGCC 0 ACGGCCCACCCAGCTCGACCCCC 0 - ILLUMINA NA 172 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_2 Homo sapiens hg19 chr19 3120987 3121177 + AGGTCCCCAGCGGGACGCCCAG 0 CAGCTCAACCTCAAGGAGTACAACCT 0 + ILLUMINA NA 187 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_3 Homo sapiens hg19 chr19 3120987 3121177 - AAAAATCTCCTCCCGCGGGCAGAG 0 AGGATGGTGTCCTTCACGGCCGC 0 - ILLUMINA NA 185 TRUE +GNAQ_4 GNAQ_4.chr9.80412436.80412564 GNAQ_4.chr9.80412436.80412564_tile_1 Homo sapiens hg19 chr9 80412436 80412564 - CATTCTCATTGTGTCTTCCCTCCTCTA 0 GTAACTGAGTCCATGAAACCTATTTCC 0 - ILLUMINA NA 188 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_1 Homo sapiens hg19 chr9 80409379 80409508 - GCTTAGTGAATATGATCAAGTTCTCGTGG 0 GCTTTCTTGAAATTTGATTTTAGGACTTTT 0 - ILLUMINA NA 174 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_2 Homo sapiens hg19 chr9 80409379 80409508 + AGATAATAAAATGATAATCCATTGCCTGTC 0 TTGGCCCCCTACATCGACCATTCT 0 + ILLUMINA NA 177 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_3 Homo sapiens hg19 chr9 80409379 80409508 - ATTGAATTGACTTGGATGATCATCGTC 0 GGTCAGAGAGAAGAAAATGGATACACT 0 - ILLUMINA NA 182 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_1 Homo sapiens hg19 chr9 80343430 80343583 - GAAAATCATGTATTCCCATCTAGTCGACT 0 TTGCCCTGTGCAGCCTGCGTGTTGA 0 - ILLUMINA NA 172 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_2 Homo sapiens hg19 chr9 80343430 80343583 + TTCACAGCTACTGAGCTGTGGTATGA 0 AGGGGTATGTGATAATTGTTCTAAAGAGAG 0 + ILLUMINA NA 171 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_3 Homo sapiens hg19 chr9 80343430 80343583 - GGTCGTATACAAAAGATGGGTTGGACTTAT 0 GTTCCAGAACTCCTCGGTTATTCTGTT 0 - ILLUMINA NA 187 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_1 Homo sapiens hg19 chr9 80336240 80336429 - ACCATCCTCCAGTTGAACCTGAAGG 0 TTTATTGCCGTCCTGGACTCTGTGTGAGCG 0 - ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_2 Homo sapiens hg19 chr9 80336240 80336429 + CAGGGAAGGGCAGGGCGGGTGTCTA 0 ATAATTTTGTCACTGTCTGGGTTCAGG 0 + ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_3 Homo sapiens hg19 chr9 80336240 80336429 - CCAATGATGATTGAATACATTAGCAGAT 0 TACTCCCACTTCACGTGCGCCACAGAC 0 - ILLUMINA NA 177 TRUE +[Targets] +TargetA TargetB Target Number Chromosome Start Position End Position Probe Strand Sequence Species Build ID +MPL1_2.chr1.43815008.43815009_tile_1 MPL1_2.chr1.43815008.43815009_tile_1 1 chr1 43814982 43815163 + GGTGGCAGTTTCCTGCACACTACAGGTACCGCCCCCGCCAGGCAGGAGACTGGCGGTGGACCAGGTGGAGCCGAAGGCCTGTAAACAGGCATTCTTGGTTCGCTCTGTGACCCCAGATCTCCGTCCACCGCC Homo sapiens hg19 +NRAS1_7.chr1.115256528.115256531_tile_1 NRAS1_7.chr1.115256528.115256531_tile_1 1 chr1 115256500 115256680 + TCTTGTCCAGCTGTATCCAGTATGTCCAACAAACAGGTTTCACCATCTATAACCACTTGTTTTCTGTAAGAATCCTGGGGGTGTGGAGGGTAAGGGGGCAGGGAGGGAGGGAAGTTCAATTTTTATTA Homo sapiens hg19 +NRAS8_13.chr1.115258730.115258748_tile_1 NRAS8_13.chr1.115258730.115258748_tile_1 1 chr1 115258702 115258884 + TGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACACCAGCAAGAACCTGTTGGAAACCAGTAATCAGGGTTAATTGGCGAGCCACATCTACAGTACTTTAAAG Homo sapiens hg19 +ALK1.chr2.29432664.29432664_tile_1 ALK1.chr2.29432664.29432664_tile_1 1 chr2 29432636 29432822 + TCGGGCCATCCCGAAGTCTCCAATCTTGGCCACTCTTCCAGGGCCTGGACAGGTCAAGAGGCAGTTTCTGGCAGCAATGTCTCTGGGAAGAAAGGAAATGCATTTCCTAATTTTATCCCTAGGAAGATGAGTG Homo sapiens hg19 +ALK2.chr2.29443695.29443695_tile_1 ALK2.chr2.29443695.29443695_tile_1 1 chr2 29443667 29443836 + GTTGAATTTGCTGCAGAGCAGAGAGGGATGTAACCAAAATTAACTGAGCTGAGTCTGGGCAAATCTTAAACTGGGAGGAACAGGATACAAAGTTACATTTTCAGCAGCTACAATGTATA Homo sapiens hg19 +IDH1_1_2.chr2.209113112.209113113_tile_1 IDH1_1_2.chr2.209113112.209113113_tile_1 1 chr2 209113084 209113264 + ACGACCTATGATGATAGGTTTTACCCATCCACTCACAAGCCGGGGGATATTTTTGCAGATAATGGCTTCTCTGAAGACCGTGCCACCCAGAATATTTCGTATGGTGCCATTTGGTGATTTCCACATT Homo sapiens hg19 +ERBB4_1_2.chr2.212288942.212288955_tile_1 ERBB4_1_2.chr2.212288942.212288955_tile_1 1 chr2 212288912 212289100 + CCTTTCTCTAATAAATCAGGGATTTCTCGCGTTGGAATTCCATCATAGGGTTTTCCTCCAAAGGTCATCAGTTCCCATATAGTAACTCCTATATTGGAGAAAAAATTCTTACTTAAGCATATTAACAACATATGT Homo sapiens hg19 +ERBB4_3_4.chr2.212530066.212530135_tile_1 ERBB4_3_4.chr2.212530066.212530135_tile_1 1 chr2 212530036 212530210 + TGGATGGCATGGGTGGCACTCCCGATCTGGATCAGCATACTTGAAAATGAAACTGTTTGCCCCCTGTAAGCCATCTGGACATTTTTCCACACAGTTTGGGCCATCTTTAAAATGAGAGCACT Homo sapiens hg19 +ERBB4_5.chr2.212576857.212576857_tile_1 ERBB4_5.chr2.212576857.212576857_tile_1 1 chr2 212576821 212576990 + AATCCACAGTCTGAGCTGACATCAATGATCCTGTGCCAATGCCATCACAAGCTGTAGAAACAAGACTCAGAGTTAGGGGATTGAGAAACTTATTTTTGGCCAATAAATCA Homo sapiens hg19 +ERBB4_6_7.chr2.212578341.212578349_tile_1 ERBB4_6_7.chr2.212578341.212578349_tile_1 1 chr2 212578315 212578499 + CGCACACAAGAACTGGAATCTACCACAAAGTTATCTGATTAAAAAAAAAAAAAAGGTAAAATAAGCATTAATGTTAACATTCAGCAAACAAGCTCAAAACAAGATATTTTAGGGTTTAAAAATGATTAGCA Homo sapiens hg19 +ERBB4_8.chr2.212587147.212587147_tile_1 ERBB4_8.chr2.212587147.212587147_tile_1 1 chr2 212587115 212587285 + CTCCATATGTGTACTTTGCATTGAAATTGTGCTCCAGTTGAAAGGTGGTTGGATTGTAGACAAAGGTTTGGGGACACTGAGTAACACATGCTCCACTGTCATTGAAATTCATGCAGG Homo sapiens hg19 +ERBB4_9.chr2.212589811.212589811_tile_1 ERBB4_9.chr2.212589811.212589811_tile_1 1 chr2 212589783 212589957 + TGTGTCCTTAGGTCCTGAGCAGCCTCCAGCACATTCTCGATGGCAGCAGTCACTGACGTAAGGTCCGTAGCATCTGCCGTCACATTGTTCTGCACACACCGTCCTTGTCACTGCAGAAGAC Homo sapiens hg19 +ERBB4_10.chr2.212652764.212652764_tile_1 ERBB4_10.chr2.212652764.212652764_tile_1 1 chr2 212652706 212652876 + ATAATTCTACTTACATCCTGAACTACCATTTGTTGACACAAGAGTCAAGTTGGAAGGCCATGGGTTCCGAACAATATCTTGCCAATGAATGGTGTCTGCATAACAAAGGAATTT Homo sapiens hg19 +ERBB4_11.chr2.212812157.212812157_tile_1 ERBB4_11.chr2.212812157.212812157_tile_1 1 chr2 212812127 212812311 + TGTCAAGTTCTTTAATCCAAGTTCTTGAAGTCCAAAGTTTCCATCTTTTCTGTAGTTTAAAAATATTGCCAAGGCATATCGATCCTCATAAAGTTTTGTCCCACGAATAATGCGTAAATTCTCCAGAGG Homo sapiens hg19 +VHL1_2.chr3.10183797.10183817_tile_1 VHL1_2.chr3.10183797.10183817_tile_1 1 chr3 10183769 10183952 + GGCTCAACTTCGACGGCGAGCCGCAGCCCTACCCAACGCTGCCGCCTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAGGCCCGACCCAGCAGGGACGATAGCACGGTCTGAAGC Homo sapiens hg19 +VHL3_5.chr3.10188245.10188301_tile_1 VHL3_5.chr3.10188245.10188301_tile_1 1 chr3 10188217 10188401 + GGTTAACCAAACTGAATTATTTGTGCCATCTCTCAATGTTGACGGACAGCCTATTTTTGCCAATATCACACTGCCAGGTACTGACGTTTTACTTTTTAAAAAGATAAGGTTGTTGTGGTAAGTACAGGATA Homo sapiens hg19 +VHL6_8.chr3.10191480.10191506_tile_1 VHL6_8.chr3.10191480.10191506_tile_1 1 chr3 10191450 10191634 + TCTGAAAGAGCGATGCCTCCAGGTTGTCCGGAGCCTAGTCAAGCCTGAGAATTACAGGAGACTGGACATCGTCAGGTCGCTCTACGAAGATCTGGAAGACCACCCAAATGTGCAGAAAGACCTGGAGCGG Homo sapiens hg19 +MLH1.chr3.37067240.37067240_tile_1 MLH1.chr3.37067240.37067240_tile_1 1 chr3 37067212 37067394 + GGTTCGTACAGATTCCCGGGAACAGAAGCTTGATGCATTTCTGCAGCCTCTGAGCAAACCCCTGTCCAGTCAGCCCCAGGCCATTGTCACAGAGGATAAGACAGATATTTCTAGTGGCAGGGCTAGGCAG Homo sapiens hg19 +CTNNB1_1_16.chr3.41266040.41266137_tile_1 CTNNB1_1_16.chr3.41266040.41266137_tile_1 1 chr3 41266010 41266180 + ATGGCCATGGAACCAGACAGAAAAGCGGCTGTTAGTCACTGGCAGCAACAGTCTTACCTGGACTCTGGAATCCATTCTGGTGCCACTACCACAGCTCCTTCTCTGAGTGGTAAAGGC Homo sapiens hg19 +PIK3CA1.chr3.178916876.178916876_tile_1 PIK3CA1.chr3.178916876.178916876_tile_1 1 chr3 178916836 178917024 + TGATGAAACAAGACGACTTTGTGACCTTCGGCTTTTTCAACCCTTTTTAAAAGTAATTGAACCAGTAGGCAACCGTGAAGAAAAGATCCTCAATCGAGAAATTGGTATGATACAATATCCTATTCTAAAATGCAAA Homo sapiens hg19 +PIK3CA2.chr3.178921553.178921553_tile_1 PIK3CA2.chr3.178921553.178921553_tile_1 1 chr3 178921525 178921709 + ATGTAAATATTCGAGACATTGATAAGGTAAAGTCAAATGCTGATGCTTATTATTTTATAGAAATTATTTTAGATAACCTTTTTCTTGCACTATACAGTAATCTGTTGACCTGTAGTATGTTTTCAGATGGT Homo sapiens hg19 +PIK3CA3.chr3.178927980.178927980_tile_1 PIK3CA3.chr3.178927980.178927980_tile_1 1 chr3 178927906 178928082 + TTATAATTTAGACTAGTGAATATTTTTCTTTGTTTTTTAAGGAACACTGTCCATTGGCATGGGGAAATATAAACTTGTTTGATTACACAGACACTCTAGTATCTGGAAAAATGGCTTTGAATC Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 1 chr3 178936044 178936214 + ATCCTCTCTCTGAAATCACTGAGCAGGAGAAAGATTTTCTATGGAGTCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGAATTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 1 chr3 178938832 178939004 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTCTCAAACAGGAGAAGAAGGATGAAACACAAAAGGTGTGTGACTCTAGTTTGTGTTTGAGACTCTT Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_1 PIK3CA13_20.chr3.178952007.178952150_tile_1 1 chr3 178951881 178952054 + TATCTAGCTATTCGACAGCATGCCAATCTCTTCATAAATCTTTTCTCAATGATGCTTGGCTCTGGAATGCCAGAACTACAATCTTTTGATGACATTGCATACATTCGAAAGACCCTAGCC Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_2 PIK3CA13_20.chr3.178952007.178952150_tile_2 1 chr3 178951999 178952184 - TTTCAGTTCAATGCATGCTGTTTAATTGTGTGGAAGATCCAATCCATTTTTGTTGTCCAGCCACCATGATGTGCATCATTCATTTGTTTCATGAAATACTCCAAAGCCTCTTGCTCAGTTTTATCTAAG Homo sapiens hg19 +FGFR3_1_2.chr4.1803564.1803568_tile_1 FGFR3_1_2.chr4.1803564.1803568_tile_1 1 chr4 1803538 1803712 + GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTGCCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTGGAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCCACATCCAGTGGCT Homo sapiens hg19 +FGFR3_3_4.chr4.1806119.1806153_tile_1 FGFR3_3_4.chr4.1806119.1806153_tile_1 1 chr4 1806091 1806277 + CGGGGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTGTGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGGCCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCCCGCTCAAGCGACAGGTA Homo sapiens hg19 +FGFR3_5_7.chr4.1807862.1807890_tile_1 FGFR3_5_7.chr4.1807862.1807890_tile_1 1 chr4 1807836 1808025 + CCGGGACGTGCACAACCTCGACTACTACAAGAAGACGACCAACGTGAGCCCGGCCCTGGGGTGCGGGGGTGGGGGTCATGCCAGTAGGACGCCTGGCGCCAACACCGCCTTCCCACACCCTCCCAGGGCCGGCTGCCCGTGA Homo sapiens hg19 +FGFR3_8.chr4.1808331.1808331_tile_1 FGFR3_8.chr4.1808331.1808331_tile_1 1 chr4 1808295 1808464 + GCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCTTCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCCCGCCAACTGCACACACGACCTGTGAGTGGCATCCCTGGCCCTCCACTGGGTCC Homo sapiens hg19 +FGFR3_9.chr4.1808949.1808949_tile_1 FGFR3_9.chr4.1808949.1808949_tile_1 1 chr4 1808921 1809105 + CCTGCTGCCCCCGGCCCCACCCAGCAGTGGGGGCTCGCGGACGTGAAGGGCCACTGGTCCCCAACAATGTGAGGGGTCCCTAGCAGCCCACCCTGCTGCTGGTGCACAGCCACTCCCCGGCATGAGACTCAGTGC Homo sapiens hg19 +PDGFRA1_4.chr4.55141013.55141049_tile_1 PDGFRA1_4.chr4.55141013.55141049_tile_1 1 chr4 55140981 55141157 + AAACCGAGGTATGAAATTCGCTGGAGGGTCATTGAATCAATCAGCCCAGATGGACATGAATATATTTATGTGGACCCGATGCAGCTGCCTTATGACTCAAGATGGGAGTTTCCAAGAGATGGA Homo sapiens hg19 +PDGFRA5.chr4.55144146.55144146_tile_1 PDGFRA5.chr4.55144146.55144146_tile_1 1 chr4 55144120 55144306 + AACTTGCTGGGAGCCTGCACCAAGTCAGGTGGGCTCACTGACCTGGAGTGAGGATTTTCACTGGACACATGTGGTTGTGAAAACTGTTCAATCAGGCTTAAATCCTCCACTCTCCATCCCCACACATGGCAGGG Homo sapiens hg19 +PDGFRA6.chr4.55144547.55144547_tile_1 PDGFRA6.chr4.55144547.55144547_tile_1 1 chr4 55144519 55144703 + CACAGAGTATTGCTTCTATGGAGATTTGGTCAACTATTTGCATAAGAATAGGGATAGCTTCCTGAGCCACCACCCAGAGAAGCCAAAGAAAGAGCTGGATATCTTTGGATTGAACCCTGCTGATGAAAGCAC Homo sapiens hg19 +PDGFRA7_23.chr4.55152040.55152109_tile_1 PDGFRA7_23.chr4.55152040.55152109_tile_1 1 chr4 55152012 55152184 + CGTCCTCCTGGCACAAGGAAAAATTGTGAAGATCTGTGACTTTGGCCTGGCCAGAGACATCATGCATGATTCGAACTATGTGTCGAAAGGCAGTGTACGTCCTCACTTCCCTCACTGGTCA Homo sapiens hg19 +KIT1.chr4.55561764.55561764_tile_1 KIT1.chr4.55561764.55561764_tile_1 1 chr4 55561736 55561913 + CGACGAGATTAGGCTGTTATGCACTGATCCGGGCTTTGTCAAATGGACTTTTGAGATCCTGGATGAAACGAATGAGAATAAGCAGAATGAATGGATCACGGAAAAGGCAGAAGCCACCAACACCG Homo sapiens hg19 +KIT2.chr4.55592185.55592186_tile_1 KIT2.chr4.55592185.55592186_tile_1 1 chr4 55592155 55592341 + CCTATTTTAACTTTGCATTTAAAGGTAACAACAAAGGTATATTTCTTTTTAATCCAATTTAAGGGGATGTTTAGGCTCTGTCTACCATATCAGTCATGATTTTAAGTTCATTCCAACATTGACCATGTCATTTC Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_1 KIT3_19.chr4.55593464.55593689_tile_1 1 chr4 55593342 55593512 + ATTTCTCTTCCATTGTAGAGCAAATCCATCCCCACACCCTGTTCACTCCTTTGCTGATTGGTTTCGTAATCGTAGCTGGCATGATGTGCATTATTGTGATGATTCTGACCTACAAATA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_2 KIT3_19.chr4.55593464.55593689_tile_2 1 chr4 55593436 55593609 - TTCTGTGGGGAGAAAGGGAAAAATAGATCACCTTTTAATAATTATTGTCTCAGTCATTAGAGCACTCTGGAGAGAGAACAAATAAATGGTTACCTGTAAATATTTGTAGGTCAGAATCATCA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_3 KIT3_19.chr4.55593464.55593689_tile_3 1 chr4 55593556 55593739 + AACCCATGTATGAAGTACAGTGGAAGGTTGTTGAGGAGATAAATGGAAACAATTATGTTTACATAGACCCAACACAACTTCCTTATGATCACAAATGGGAGTTTCCCAGAAACAGGCTGAGTTTTGGTCAG Homo sapiens hg19 +KIT20_21.chr4.55594221.55594258_tile_1 KIT20_21.chr4.55594221.55594258_tile_1 1 chr4 55594193 55594380 + CAAAGTCCTGAGTTACCTTGGTAATCACATGAATATTGTGAATCTACTTGGAGCCTGCACCATTGGAGGTAAAGCCGTGTCCAAGCTGCCTTTTATTGTCTGTCAGGTTATCAAAACATGACATTTTAATATG Homo sapiens hg19 +KIT22.chr4.55595519.55595519_tile_1 KIT22.chr4.55595519.55595519_tile_1 1 chr4 55595493 55595675 + CAGAATATTGTTGCTATGGTGATCTTTTGAATTTTTTGAGAAGAAAACGTGATTCATTTATTTGTTCAAAGCAGGAAGATCATGCAGAAGCTGCACTTTATAAGAATCTTCTGCATTCAAAGGAGTCT Homo sapiens hg19 +KIT23.chr4.55597495.55597497_tile_1 KIT23.chr4.55597495.55597497_tile_1 1 chr4 55597467 55597652 + CAGCGATAGTACTAATGAGTACATGGACATGAAACCTGGAGTTTCTTATGTTGTCCCAACCAAGGCCGACAAAAGGAGATCTGTGAGAATAGGTGAGTACCTACCTATCAAGCAACCAAGAGTAACTTTAC Homo sapiens hg19 +KIT24_28.chr4.55599320.55599348_tile_1 KIT24_28.chr4.55599320.55599348_tile_1 1 chr4 55599290 55599472 + AGAGACATCAAGAATGATTCTAATTATGTGGTTAAAGGAAACGTGAGTACCCATTCTCTGCTTGACAGTCCTGCAAAGGATTTTTAGTTTCAACTTTCGATAAAAATTGTTTCCTGTGATTTTCATAAT Homo sapiens hg19 +KIT29.chr4.55602694.55602694_tile_1 KIT29.chr4.55602694.55602694_tile_1 1 chr4 55602666 55602850 + CCTGAAAGCATTTTCAACTGTGTATACACGTTTGAAAGTGACGTCTGGTCCTATGGGATTTTTCTTTGGGAGCTGTTCTCTTTAGGTAAAATGATCCTTGCCAAAGACAACTTCATTAGACTCAGAGCATCTT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_1 KDR1.chr4.55946114.55946257_tile_1 1 chr4 55945984 55946155 + CGGCTACTTCCTGCTGGTGGAAAGAACAACACTTGAAAATCTGAGCAGCACCTCTCATGTGATGTCCAGGAGTTGGGGGTGTGGATGCTTCCTTTTAAACAGGAGGAGAGCT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_2 KDR1.chr4.55946114.55946257_tile_2 1 chr4 55946098 55946284 - GGATATCACTCCGATGACACAGACACCACCGTGTACTCCAGTGAGGAAGCAGAACTTTTAAAGCTGATAGAGATTGGAGTGCAAACCGGTAGCACAGCCCAGATTCTCCAGCCTGACTCGGGGACCACACTGA Homo sapiens hg19 +KDR3.chr4.55953807.55953807_tile_1 KDR3.chr4.55953807.55953807_tile_1 1 chr4 55953777 55953965 + TTGGGGTCACATACTTCCTCCTCCTCCATACAGGAAACAGGTGAGGTAGGCAGAGAGAGTCCAGAATCCTCTTCCATGCTCAAAGTCTCTGATATCGGAAGAACAATGTAGTCTTTGCCATCCTGAAACAATAAA Homo sapiens hg19 +KDR4.chr4.55955111.55955127_tile_1 KDR4.chr4.55955111.55955127_tile_1 1 chr4 55955085 55955257 + CCCCGTGCCAGCAGTCCAGCATGGTCTGGTACCTAGAGAAGCAAAACACTGATTTCATTAAATGCCTCTTTCTTCCTGAATGCTGAAAATAAGCACTTAAATGAGTACACATTTGTAAAGAG Homo sapiens hg19 +KDR6.chr4.55960989.55961023_tile_1 KDR6.chr4.55960989.55961023_tile_1 1 chr4 55960959 55961129 + TCACTGAGGGACTTCTCCTCCACAAATCCAGAGCTGGCTGAGCTCTGGCTACTGGTGATGCTGTCCAAGCGCCGTTTCAGATCCACAGGGATTGCTCCAACGTAGTCTTTCCCTTGA Homo sapiens hg19 +KDR8.chr4.55962507.55962507_tile_1 KDR8.chr4.55962507.55962507_tile_1 1 chr4 55962477 55962653 + GCTCCTTCTACAAATACAGTACAAAGAGGGAAATCATAGGTATGGACATTTCCTTCAATAATTGGGGTCCCTCCCTCCCTGCATGCCACTATACAACTTACCCTCCGGGGTAACACAGCTGTGA Homo sapiens hg19 +KDR9.chr4.55972964.55972964_tile_1 KDR9.chr4.55972964.55972964_tile_1 1 chr4 55972936 55973106 + ACTGAGACAGCTTGGCTATAAGAAAGAGATAACAGCGCATATTATGATTTAATTTTTCTTTAATTAGAGTCAAGAGTAAGGAAAAGATTCAGACTTTGGTTATTCTGTTCTTAGAAA Homo sapiens hg19 +KDR10.chr4.55979623.55979623_tile_1 KDR10.chr4.55979623.55979623_tile_1 1 chr4 55979595 55979775 + CTCGGTTTACAAGTTTCTTATGCTGATGCTGAAAAAAAGAGTTGACTGAACTTCCAAAGCACAGCATATAACATTACCCAATAACTTCTAGTAACACACAGAATTAAATCTGGGCTTTGGTAAACATT Homo sapiens hg19 +KDR11.chr4.55980348.55980348_tile_1 KDR11.chr4.55980348.55980348_tile_1 1 chr4 55980320 55980496 + TGCTGTACAATTTAAGACAAGCTTTTCTCCAACAGATAGTTCAATTCCATGAGACGGACTCAGAACCACATCATAAATCCTATACCCTAGAGCAAGTAAATTGAAAAAACAGAACATGAGAGA Homo sapiens hg19 +FBXW7_1.chr4.153245446.153245446_tile_1 FBXW7_1.chr4.153245446.153245446_tile_1 1 chr4 153245416 153245604 + AACGACTGGTGCCCTGTTAACGTGTGAATGCAATTCCCTGTCTCCACATCCCAAACACGGATTGATGTATCAAGAGATCCACTCACCACATGGATACCATCAAACTACAAAAGACACAGTTTATTAGAATAGA Homo sapiens hg19 +FBXW7_2.chr4.153247288.153247366_tile_1 FBXW7_2.chr4.153247288.153247366_tile_1 1 chr4 153247248 153247417 + TTGAACACAGCGGACTGCTGCAACATGACCCATCAAAACATGTAAACACTGGCCTGTCTCAATATCCCAAACCCTAAGAGTGGCATCTCGAGAACCGCTAACAACTCTGCAG Homo sapiens hg19 +FBXW7_5.chr4.153249384.153249384_tile_1 FBXW7_5.chr4.153249384.153249384_tile_1 1 chr4 153249338 153249520 + TTCATGAAGATGCATACAACGCACAGTGGAAGTATGCCCATATAAGGTGTGTATACATTCTCCAGTCTCTGCATTCCACACTTTGAGTGTCCGATCTGTAGATCCACTAATGATGATGTTGTCTCTCAT Homo sapiens hg19 +FBXW7_7.chr4.153250883.153250883_tile_1 FBXW7_7.chr4.153250883.153250883_tile_1 1 chr4 153250853 153251031 + ATTCGGTTACCACAAAACTGTAAGCATGTGATCACATGATCATCATGTCCTTTCAGCACCTATAAGAAAGATGTGCAGATTAGAAATATGTTAATTAAATTATGTTCTTTAAAATACTGGTGAAGA Homo sapiens hg19 +FBXW7_8.chr4.153258983.153258983_tile_1 FBXW7_8.chr4.153258983.153258983_tile_1 1 chr4 153258953 153259142 + TCGTTGAAACTGGGGTTCTATCACTTGCATCATATGTTTTACTTGTGTTGGTTCACAACTATCAATGAGTTCATCTAAAGCAAGCAATTTCTCTGGTCCACTCCAGCTCTATCAAAGAGAATTAGAAATTTT Homo sapiens hg19 +APC1.chr5.112173917.112173917_tile_1 APC1.chr5.112173917.112173917_tile_1 1 chr5 112173887 112174071 + AAGCGAGGTTTGCAGATCTCCACCACTGCAGCCCAGATTGCCAAAGTCATGGAAGAAGTGTCAGCCATTCATACCTCTCAGGAAGACAGAAGTTCTGGGTCTACCACTGAATTACATTGTGTGACAGATGA Homo sapiens hg19 +APC2.chr5.112174631.112174631_tile_1 APC2.chr5.112174631.112174631_tile_1 1 chr5 112174603 112174775 + TCGAGTGGGTTCTAATCATGGAATTAATCAAAATGTAAGCCAGTCTTTGTGTCAAGAAGATGACTATGAAGATGATAAGCCTACCAATTATAGTGAACGTTACTCTGAAGAAGAACAGC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_1 APC3_42.chr5.112175162.112175958_tile_1 1 chr5 112175034 112175208 - TCTGCTTCCTGTGTCGTCTGATTACATCCTATTTCATCTTCAGCTGATGACAAAGATGATAATGAACTACATCTTGAAAAACATATTGGAGTATCTTCTACACAATAAGTCTGTATTGTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_2 APC3_42.chr5.112175162.112175958_tile_2 1 chr5 112175128 112175297 + ATGTAATCAGACGACACAGGAAGCAGATTCTGCTAATACCCTGCAAATAGCAGAAATAAAAGAAAAGATTGGAACTAGGTCAGCTGAAGATCCTGTGAGCGAAGTTCCAGCAGTGTCAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_3 APC3_42.chr5.112175162.112175958_tile_3 1 chr5 112175216 112175386 - CCTGAAGAAAATTCAACAGCTTTGTGCCTGGCTGATTCTGAAGATAAACTAGAACCCTGCAGTCTGCTGGATTTGGTTCTAGGGTGCTGTGACACTGCTGGAACTTCGCTCACAGGAT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_4 APC3_42.chr5.112175162.112175958_tile_4 1 chr5 112175306 112175475 + CACAAAGCTGTTGAATTTTCTTCAGGAGCGAAATCTCCCTCCAAAAGTGGTGCTCAGACACCCAAAAGTCCACCTGAACACTATGTTCAGGAGACCCCACTCATGTTTAGCA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_5 APC3_42.chr5.112175162.112175958_tile_5 1 chr5 112175394 112175566 - GCCACTTACCATTCCACTGCATGGTTCACTCTGAACGGAGCTGGCAATCGAACGACTCTCAAAACTATCAAGTGAACTGACAGAAGTACATCTGCTAAACATGAGTGGGGTCTCCTGAAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_6 APC3_42.chr5.112175162.112175958_tile_6 1 chr5 112175512 112175683 + GCATTATAAGCCCCAGTGATCTTCCAGATAGCCCTGGACAAACCATGCCACCAAGCAGAAGTAAAACACCTCCACCACCTCCTCAAACAGCTCAAACCAAGCGAGAAGTACCTAAAAATA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_7 APC3_42.chr5.112175162.112175958_tile_7 1 chr5 112175630 112175799 - CCGTGGCAAAATGTAATAAAGTATCAGCATCTGGAAGAACCTGGACCCTCTGAACTGCAGCATTTACTGCAGCTTGCTTAGGTCCACTCTCTCTCTTTTCAGCAGTAGGTGCTTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_8 APC3_42.chr5.112175162.112175958_tile_8 1 chr5 112175740 112175911 + GGAAAGTACTCCAGATGGATTTTCTTGTTCATCCAGCCTGAGTGCTCTGAGCCTCGATGAGCCATTTATACAGAAAGATGTGGAATTAAGAATAATGCCTCCAGTTCAGGAA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_9 APC3_42.chr5.112175162.112175958_tile_9 1 chr5 112175854 112176042 - AGTATTTCAATATCATCATCATCTGAATCATCTAATAGGTCCTTTTCAGAATCAATAGTTTTTTCTGCCTCTTTCTCTTGGTTTTCATTTGATTCTTTAGGCTGCTCTGATTCTGTTTCATTCCCATTGTCATTT Homo sapiens hg19 +CSF1R1_3.chr5.149433644.149433646_tile_1 CSF1R1_3.chr5.149433644.149433646_tile_1 1 chr5 149433616 149433799 + GATAGTTGTTGGGCTGCAGCAAGGGCTGGGCGATATCCCCTTGCTCGCAGCAGGTCAGGTGCTCACTAGAGCTCTCCTCCTCCAGCTCACTGCTGCTGCTGCCGCTGCCACCGCTTCTGCTGCTGCTCGGC Homo sapiens hg19 +CSF1R4.chr5.149453044.149453044_tile_1 CSF1R4.chr5.149453044.149453044_tile_1 1 chr5 149453016 149453189 + CAAGTAGGCACTCTCTGGAAAGCAGAACACACAAGCATCTGGCATTAGTGGGAAGATGTCCTTGTTTATTTGTCCATTTTGTCATCCACCCATTGATCCAGTCCCTGAGCAGCTATGTCAC Homo sapiens hg19 +NPM1.chr5.170837547.170837548_tile_1 NPM1.chr5.170837547.170837548_tile_1 1 chr5 170837493 170837677 + TTTTTTTTCCAGGCTATTCAAGATCTCTGGCAGTGGAGGAAGTCTCTTTAAGAAAATAGTTTAAACAATTTGTTAAAAAATTTTCCGTCTTATTTCATTTCTGTAACAGTTGATATCTGGCTGTCCTTTTTA Homo sapiens hg19 +EGFR1.chr7.55211080.55211080_tile_1 EGFR1.chr7.55211080.55211080_tile_1 1 chr7 55211052 55211238 + AGAGGAAATATGTACTACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATGATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAGAAATTTACAGGGTGAGAGGCTGGGATGCCAAGGCTGGGGGT Homo sapiens hg19 +EGFR2.chr7.55221822.55221822_tile_1 EGFR2.chr7.55221822.55221822_tile_1 1 chr7 55221792 55221964 + GGTGCCACCTGCGTGAAGAAGTGTCCCCGTGAGTCCTCCTCTGTGGGCCCTCTAACTGGTCAGGCATCCTTGTCCCGCTCTGTCTCCTGCTGAGCCCTGGAGTATCCCATCTTGGAGAGT Homo sapiens hg19 +EGFR3.chr7.55233043.55233043_tile_1 EGFR3.chr7.55233043.55233043_tile_1 1 chr7 55233019 55233203 + GGAGTCATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCAGACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTGCACCTACGGGTGAGTGGAAAGTGAAGGAGAACAGAACATTTCCTCTCTTGCAAAT Homo sapiens hg19 +EGFR4.chr7.55241677.55241708_tile_1 EGFR4.chr7.55241677.55241708_tile_1 1 chr7 55241649 55241827 + AGGAAACTGAATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTTCGGCACGGTGTATAAGGTAAGGTCCCTGGCACAGGCCTCTGGGCTGGGCCGCAGGGCCTCTCATGGTCTGGTGGGGAGCC Homo sapiens hg19 +EGFR9.chr7.55242418.55242511_tile_1 EGFR9.chr7.55242418.55242511_tile_1 1 chr7 55242388 55242576 + GACTCTGGATCCCAGAAGGTGAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCTCGATGTGAGTTTCTGCTTTGCTGTGTGGGGGTCCATGGCT Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_1 EGFR44.chr7.55249005.55249131_tile_1 1 chr7 55248879 55249052 + TCTTCACCTGGAAGGGGTCCATGTGCCCCTCCTTCTGGCCACCATGCGAAGCCACACTGACGTGCCTCTCCCTCCCTCCAGGAAGCCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTG Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_2 EGFR44.chr7.55249005.55249131_tile_2 1 chr7 55249003 55249178 - CAGTTGAGCAGGTACTGGGAGCCAATATTGTCTTTGTGTTCCCGGACATAGTCCAGGAGGCAGCCGAAGGGCATGAGCTGCGTGATGAGCTGCACGGTGGAGGTGAGGCAGATGCCCAGCAGGCGGC Homo sapiens hg19 +EGFR54.chr7.55259514.55259524_tile_1 EGFR54.chr7.55259514.55259524_tile_1 1 chr7 55259486 55259662 + GCTGGCCAAACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAGAAGGAGGCAAAGTAAGGAGGTGGCTTTAGGTCAGCCAGCATTTTCCTGACACCAGGGACCAGGCTGCCTTCCCACTAGC Homo sapiens hg19 +MET1.chr7.116339642.116339642_tile_1 MET1.chr7.116339642.116339642_tile_1 1 chr7 116339614 116339792 + AGCCCAGCCAGTGTCCTGACTGTGTGGTGAGCGCCCTGGGAGCCAAAGTCCTTTCATCTGTAAAGGACCGGTTCATCAACTTCTTTGTAGGCAATACCATAAATTCTTCTTATTTCCCAGATCAT Homo sapiens hg19 +MET2.chr7.116340262.116340262_tile_1 MET2.chr7.116340262.116340262_tile_1 1 chr7 116340234 116340420 + AACAAGATCGTCAACAAAAACAATGTGAGATGTCTCCAGCATTTTTACGGACCCAATCATGAGCACTGCTTTAATAGGGTAAGTCACATCAGTTCCCCACTTATAAACTGTGAGGTATAAATTAGAAATAAGT Homo sapiens hg19 +MET3.chr7.116411990.116411990_tile_1 MET3.chr7.116411990.116411990_tile_1 1 chr7 116411958 116412127 + GCCCAACTACAGAAATGGTTTCAAATGAATCTGTAGACTACCGAGCTACTTTTCCAGAAGGTATATTTCAGTTTATTGTTCTGAGAAATACCTATACATATACCTCAGTGGGTTGT Homo sapiens hg19 +MET4.chr7.116417463.116417464_tile_1 MET4.chr7.116417463.116417464_tile_1 1 chr7 116417431 116417620 + TATATCATGGGACTTTGTTGGACAATGATGGCAAGAAAATTCACTGTGCTGTGAAATCCTTGAACAGTAAGTGGCATTTTATTTAACCATGGAGTATACTTTTGTGGTTTGCAACCTAATAAATAGCTTATAATA Homo sapiens hg19 +MET6.chr7.116423413.116423474_tile_1 MET6.chr7.116423413.116423474_tile_1 1 chr7 116423385 116423555 + TGTATGATAAAGAATACTATAGTGTACACAACAAAACAGGTGCAAAGCTGCCAGTGAAGTGGATGGCTTTGGAAAGTCTGCAAACTCAAAAGTTTACCACCAAGTCAGATGTGGTAAT Homo sapiens hg19 +SMO1.chr7.128845101.128845101_tile_1 SMO1.chr7.128845101.128845101_tile_1 1 chr7 128845073 128845257 + GGTTCGGACAGACAACCCCAAGAGCTGGTACGAGGACGTGGAGGGCTGCGGCATCCAGTGCCAGAACCCGCTCTTCACAGAGGCTGAGCACCAGGACATGCACAGCTACATCGCGGCCTTCGGGGCCGTCACGGGC Homo sapiens hg19 +SMO2.chr7.128846040.128846040_tile_1 SMO2.chr7.128846040.128846040_tile_1 1 chr7 128846010 128846194 + TACGCCCTGATGGCTGGTGTGGTTTGGTTTGTGGTCCTCACCTATGCCTGGCACACTTCCTTCAAAGCCCTGGGCACCACCTACCAGCCTCTCTCGGGCAAGACCTCCTACTTCCACCTGCTCACCTGGTC Homo sapiens hg19 +SMO3.chr7.128846374.128846374_tile_1 SMO3.chr7.128846374.128846374_tile_1 1 chr7 128846348 128846536 + CGTGCTGGCCCCAATCGGCCTGGTGCTCATCGTGGGAGGCTACTTCCTCATCCGAGGTGAGTGAAGACCAGGCCAGGACCAGTTGGGCAACAAAATATACTGGGCACTTGCTGCCAGTACTGGGAGCTGCCAGCACG Homo sapiens hg19 +SMO4.chr7.128850341.128850341_tile_1 SMO4.chr7.128850341.128850341_tile_1 1 chr7 128850311 128850499 + GCACCTGGGTCTGGACCAAGGCCACGCTGCTCATCTGGAGGCGTACCTGGTGCAGGTGGGCATGGCAGCCAGCCCCTCCTGCCCTGCCCGCCTCACCCTCAGCCTTGGGACCCCATCTTTAGGTTTTGTCGGGTCCTG Homo sapiens hg19 +SMO5.chr7.128851593.128851593_tile_1 SMO5.chr7.128851593.128851593_tile_1 1 chr7 128851563 128851734 + GTCACCCCTGTGGCAACTCCAGGTATGAGAGTTCAAGCTTCTGGAGGAAGGTGGGGGGAGCACAGAGGCTGGGGGCTTCTGGGACTGGAGTACAGGGGCTGTCGGAGGAGGAGGAAGAG Homo sapiens hg19 +BRAF1.chr7.140453121.140453193_tile_1 BRAF1.chr7.140453121.140453193_tile_1 1 chr7 140453093 140453267 + CACTCCATCGAGATTTCACTGTAGCTAGACCAAAATCACCTATTTTTACTGTGAGGTCTTCATGAAGAAATATATCTGAGGTGTAGTAAGTAAAGGAAAACAGTAGATCTCATTTTCCTATC Homo sapiens hg19 +BRAF28.chr7.140481397.140481478_tile_1 BRAF28.chr7.140481397.140481478_tile_1 1 chr7 140481369 140481545 + ACTGTTCCAAATGATCCAGATCCAATTCTTTGTCCCACTGTAATCTGCCCATCAGGAATCTCCCAATCATCACTCGAGTCCCGTCTACCAAGTGTTTTCTTGATAAAAACAGTAAAAAAGTCA Homo sapiens hg19 +FGFR1_1.chr8.38282209.38282209_tile_1 FGFR1_1.chr8.38282209.38282209_tile_1 1 chr8 38282183 38282360 + GGGGACCGCTCTGTGGAAGATGGGAGAGGAGGCACTTGTCATGGGGACCTTGCCATGGCTAAAGAGGGGTGGGCTCACCTGCGCCCCACTTGGCTTTCCCAGTGATGGGTTGTAAACCTCCCAGCAC Homo sapiens hg19 +FGFR1_2.chr8.38285938.38285938_tile_1 FGFR1_2.chr8.38285938.38285938_tile_1 1 chr8 38285908 38286090 + TCCGAGGAGGGGAGAGCATCTATGGGAAGAAGAAGGGGCACTGAGGTTCCTCCTAGGGACCCCTAGATTTCACCAAGGCTAGTGCAGTTCCAGATGAACACGGACACCCTCCCCATGGGGATCCCAGTC Homo sapiens hg19 +JAK2_1.chr9.5073769.5073770_tile_1 JAK2_1.chr9.5073769.5073770_tile_1 1 chr9 5073737 5073923 + TATGTGTCTGTGGAGACGAGAGTAAGTAAAACTACAGGCTTTCTAATGCCTTTCTCAGAGCATCTGTTTTTGTTTATATAGAAAATTCAGTTTCAGGATCACAGCTAGGTGTCAGTGTAAACTATAATTT Homo sapiens hg19 +CDKN2A1.chr9.21971153.21971187_tile_1 CDKN2A1.chr9.21971153.21971187_tile_1 1 chr9 21971123 21971308 + GGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGCCAGGGTGGGGGCCGGCATGACGGAAAGGAAGCTTGTGTAGAGCCCCC Homo sapiens hg19 +ABL1_1.chr9.133738330.133738364_tile_1 ABL1_1.chr9.133738330.133738364_tile_1 1 chr9 133738302 133738491 + CCATGAAGCACAAGCTGGGCGGGGGCCAGTACGGGGAGGTGTACGAGGGCGTGTGGAAGAAATACAGCCTGACGGTGGCCGTGAAGACCTTGAAGGTAGGCTGGGACTGCCGGGGGTGCCCAGGGTACGTGGGGCAAG Homo sapiens hg19 +ABL1_9.chr9.133747520.133747520_tile_1 ABL1_9.chr9.133747520.133747520_tile_1 1 chr9 133747476 133747664 + TTTCCTTCTGCAGGAGGACACCATGGAGGTGGAAGAGTTCTTGAAAGAAGCTGCAGTCATGAAAGAGATCAAACACCCTAACCTGGTGCAGCTCCTTGGTGAGTAAGCCCGGGGCTCTGAAGAGAGGGTCTCGCGCCGC Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_1 ABL1_10.chr9.133748283.133748414_tile_1 1 chr9 133748157 133748327 - CCCGTAGGTCATGAACTCAGTGATGATATAGAACGGGGGCTCCCGGGTGCAGACCCCTGCCAACAAGACAACGAGGACTTCAACACGTGGCTCCGCTCCCAACTGAACAAACAACT Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_2 ABL1_10.chr9.133748283.133748414_tile_2 1 chr9 133748277 133748457 + GAACCTCCTGGACTACCTGAGGGAGTGCAACCGGCAGGAGGTGAACGCCGTGGTGCTGCTGTACATGGCCACTCAGATCTCGTCAGCCATGGAGTACCTGGAGAAGAAAAACTTCATCCACAGGTAGGGGCCT Homo sapiens hg19 +ABL1_16.chr9.133750356.133750356_tile_1 ABL1_16.chr9.133750356.133750356_tile_1 1 chr9 133750328 133750516 + GCCCATGCTGGAGCCAAGTTCCCCATCAAATGGACTGCACCCGAGAGCCTGGCCTACAACAAGTTCTCCATCAAGTCCGACGTCTGGGGTAAGGGCTGCTGCTGCACTGAAGTGGTCCTTCCTGACTACAGGAGGGTT Homo sapiens hg19 +NOTCH1_1.chr9.139397768.139397768_tile_1 NOTCH1_1.chr9.139397768.139397768_tile_1 1 chr9 139397740 139397928 + CCAGGTAGACGATGGAGCTGGGCGGACAATCAGAGAGGGGCTGGGACCCGAGGCTTCCTCCTCCCCCGCCCACCGGCCAGGGATGCTGCCGCAGGACACTGAGGCCCATGACGCCACAGTCAGGACATGGTGAGGC Homo sapiens hg19 +NOTCH1_2.chr9.139399344.139399422_tile_1 NOTCH1_2.chr9.139399344.139399422_tile_1 1 chr9 139399316 139399485 + GCAGCACGCGGCTGAGCTCCCGCAGGAAGTGGAAGGAGCTGTTGCGCAGCTGCTCCGGCGGCATCAGCACCACCACCACCAGCGTGCCGGCCGCCAGCCTCTCGGGTACATGCTCCGC Homo sapiens hg19 +RET1.chr10.43609078.43609104_tile_1 RET1.chr10.43609078.43609104_tile_1 1 chr10 43609048 43609226 + CTGCTTCCCTGAGGAGGAGAAGTGCTTCTGCGAGCCCGAAGACATCCAGGGTGAGTGGGTGGCGGCCGGGACCACCACCACCTCCCAGCCCCACAGAGGTCTCAACAGCACATCTGAGGTCCCAACAA Homo sapiens hg19 +RET2_9.chr10.43609940.43609950_tile_1 RET2_9.chr10.43609940.43609950_tile_1 1 chr10 43609902 43610075 - TGGCTTGTGGGCAAACTTGTGGTAGCAGTGGATGCAGAAGGCAGACAGCAGCACCGAGACGATGAAGGAGAAGAGGACAGCGGCTGCGATCACCGTGCGGCACAGCTCGTCGCACAGTGG Homo sapiens hg19 +RET10.chr10.43613840.43613840_tile_1 RET10.chr10.43613840.43613840_tile_1 1 chr10 43613810 43613998 + CGAGTGAGCTGCGAGACCTGCTGTCAGAGTTCAACGTCCTGAAGCAGGTCAACCACCCACATGTCATCAAATTGTATGGGGCCTGCAGCCAGGATGGTAAGGCCAGCTGCAGGGTGAGGTGGGCAGCCACTGCACCCAG Homo sapiens hg19 +RET11_12.chr10.43615567.43615569_tile_1 RET11_12.chr10.43615567.43615569_tile_1 1 chr10 43615533 43615703 + CCTGGTAGCTGAGGGGCGGAAGATGAAGATTTCGGATTTCGGCTTGTCCCGAGATGTTTATGAAGAGGATTCCTACGTGAAGAGGAGCCAGGTGCCCAGTCCCGGGGATGAGGCGGGG Homo sapiens hg19 +RET13.chr10.43617416.43617416_tile_1 RET13.chr10.43617416.43617416_tile_1 1 chr10 43617388 43617564 + ATGGCAATTGAATCCCTTTTTGATCATATCTACACCACGCAAAGTGATGTGTAAGTGTGGGTGTTGCTCTCTTGGGGTGGAGGTTACAGAAACACCCTTATACATGTAGTGGGGCCACGACGC Homo sapiens hg19 +PTEN1.chr10.89624242.89624244_tile_1 PTEN1.chr10.89624242.89624244_tile_1 1 chr10 89624214 89624388 + CAAAGAGATCGTTAGCAGAAACAAAAGGAGATATCAAGAGGATGGATTCGACTTAGACTTGACCTGTATCCATTTCTGCGGCTGCTCCTCTTTACCTTTCTGTCACTCTCTTAGAACGTGG Homo sapiens hg19 +PTEN3.chr10.89685307.89685307_tile_1 PTEN3.chr10.89685307.89685307_tile_1 1 chr10 89685275 89685459 + ATATACAATCTGTAAGTATGTTTTCTTATTTGTATGCTTGCAAATATCTTCTAAAACAACTATTAAGTGAAAGTTATCTGCTTGTTAGAGTGAGGTAGAGTTAAAGATACATTTTAACAGAATTGTATT Homo sapiens hg19 +PTEN4.chr10.89711893.89711900_tile_1 PTEN4.chr10.89711893.89711900_tile_1 1 chr10 89711865 89712039 + GTCAGAGGCGCTATGTGTATTATTATAGCTACCTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN7.chr10.89717615.89717772_tile_1 1 chr10 89717489 89717668 + ATATTGCTGATATTAATCATTAAAATCGTTTTTGACAGTTTGACAGTTAAAGGCATTTCCTGTGAAATAATACTGGTATGTATTTAACCATGCAGATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_2 PTEN7.chr10.89717615.89717772_tile_2 1 chr10 89717615 89717801 - TTTAGCATCTTGTTCTGTTTGTGGAAGAACTCTACTTTGATATCACCACACACAGGTAACGGCTGAGGGAACTCAAAGTACATGAACTTGTCTTCCCGTCGTGTGGGTCCTGAATTGGAGGAATATATCTTCACC Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 1 chr10 89720684 89720870 + CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATCGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_2 PTEN13.chr10.89720716.89720852_tile_2 1 chr10 89720814 89720991 - TTCTTCATCAGCTGTACTCCTAGAATTAAACACACATCACATACATACAAGTCAACAACCCCCACAAAATGTTTAATTTAACTGACCTTAAAATTTGGAGAAAAGTATCGGTTGGCTTT Homo sapiens hg19 +FGFR2_1.chr10.123258034.123258034_tile_1 FGFR2_1.chr10.123258034.123258034_tile_1 1 chr10 123258006 123258184 + GATTTATGATATTCTTGTGTTTCCCAATCATCTTCATCATCTCCATCTCTGACACCAGATCAGAAAGGTCTTTCTCTGTGGCATCATCTATGAACAGTAGGCATATTCACAAATCAGTTCATTTC Homo sapiens hg19 +FGFR2_2.chr10.123274774.123274803_tile_1 FGFR2_2.chr10.123274774.123274803_tile_1 1 chr10 123274746 123274930 + CAGTAAATGGCTATCTCCAGGTAGTCTGGGGAAGCTGTAATCTCCTTTTCTCTTCCAGGCGCTAGATTGCAGATCACAGGAGGAGGAACAGATAAGCAGGCCATAGAGTTAGCACACCAGACTGACGCATC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_1 FGFR2_5.chr10.123279503.123279677_tile_1 1 chr10 123279385 123279555 + AACAGGAAATCAAAGAACCTGTGGCCAAACCCATGAAGGAGACCCCAGTTGTGGGTACCTTTAGATTCAGAAAGTCCTCACCTTGAGAACCTTGAGGTAGGGCAGCCCGTCGGGCCC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_2 FGFR2_5.chr10.123279503.123279677_tile_2 1 chr10 123279471 123279640 - ACGTAGAGTTTGTCTGCAAGGTTTACAGTGATGCCCAGCCCCACATCCAGTGGATCAAGCACGTGGAAAAGAACGGCAGTAAATACGGGCCCGACGGGCTGCCCTACCTCAAGGTT Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_3 FGFR2_5.chr10.123279503.123279677_tile_3 1 chr10 123279587 123279769 + TCTCCTCCGACCACTGTGGAGGCATTTGCCGGCAGTCCGGCTTGGAGGATGGGCCGGTGAGGCGATCGCTCTGGTGGAGAGAGGGAAGAAAGGAGGAGTGGGGATGGGAGAATGAGAGACCAATAAATA Homo sapiens hg19 +HRAS1.chr11.533873.533875_tile_1 HRAS1.chr11.533873.533875_tile_1 1 chr11 533843 534021 + CCTCCTGGCCGGCGGTATCCAGGATGTCCAACAGGCACGTCTCCCCATCAATGACCACCTGCTTCCGGTAGGAATCCTGCAGGAGGACAGGGCTCAGGGACCCCCTCAGGACCTTCCGTGGGGGGA Homo sapiens hg19 +HRAS6.chr11.534285.534289_tile_1 HRAS6.chr11.534285.534289_tile_1 1 chr11 534251 534434 + GCCCACACCGCCGGCGCCCACCACCACCAGCTTATATTCCGTCATCGCTCCTCAGGGGCCTGCGGCCCGGGGTCCTCCTACAGGGTCTCCTGCCCCACCTGCCAAGGAGGGCCCTGCTCAGCCAGGCCCAGGC Homo sapiens hg19 +ATM1.chr11.108117847.108117848_tile_1 ATM1.chr11.108117847.108117848_tile_1 1 chr11 108117817 108117989 + TGTCACCAGGTACAGTAAGTAGGTCATGTCACATTTAGAAATTTCCTGTTAATTTTTTTTTTAAACTGGGCATTTTGGGCTTTTAAAACCTGTGTTCTCACAAAAAGCCTATAAAAT Homo sapiens hg19 +ATM2.chr11.108119823.108119823_tile_1 ATM2.chr11.108119823.108119823_tile_1 1 chr11 108119793 108119963 + TTGTGCCTTGGTAAAGTGTTACCATTTTCTCATTCAGTGTCATTTTAATCTCTTGTATGTTATTTTTCAGAAAACTTTCAGTGGAATCCTTTCATCTCAACCAGAACTAAGTCATTT Homo sapiens hg19 +ATM3.chr11.108123551.108123551_tile_1 ATM3.chr11.108123551.108123551_tile_1 1 chr11 108123513 108123683 + AGTAATTTTCCTCATCTTGTACTGGAGAAAATTCTTGTGAGTCTCACTATGAAAAACTGTAAAGCTGCAATGAATTTTTTCCAAAGCGTGCCAGAATGGTATGTTATCTAATA Homo sapiens hg19 +ATM4.chr11.108137973.108138003_tile_1 ATM4.chr11.108137973.108138003_tile_1 1 chr11 108137939 108138126 + TAATGGAGGTGGAGGATCAGTCATCCATGAATCTATTTAACGATTACCCTGATAGTAGTGTTAGTGATGCAAACGAACCTGGAGAGAGCCAAAGTACCATAGGTAAATACATATTTACTACTTGGGATT Homo sapiens hg19 +ATM6.chr11.108155132.108155132_tile_1 ATM6.chr11.108155132.108155132_tile_1 1 chr11 108155104 108155281 + GGCACAGCAAAGAGAGACTGCTACCAAGGTCTATGATATGCTTAAAAGTGAAAACTTATTGGGAAAACAGGTATGGCTTCAATTTTTATGTACTTTTCATTCCCTGAATGATATGAGATAT Homo sapiens hg19 +ATM7.chr11.108170476.108170479_tile_1 ATM7.chr11.108170476.108170479_tile_1 1 chr11 108170442 108170618 + GGGTCCTATAGATTTCTCTACCATAGCTATACAACATAGTAAAGATGCATCTTATACCAAGGCCCTTAAGTTATTTGAAGATAAAGAACTTCAGTGGACCTTCATAATGCTGACCTACCTGAA Homo sapiens hg19 +ATM9.chr11.108172421.108172421_tile_1 ATM9.chr11.108172421.108172421_tile_1 1 chr11 108172391 108172571 + TTAGCCACAAAGACTGGACATAGTTTCTGGGAGATTTATAAGATGACAACAGATCCAATGCTGGCCTATCTACAGCCTTTTAGAACATCAAGAAAAAAGGTCTCTTAAGTAATAAATGTTTATTGAA Homo sapiens hg19 +ATM10.chr11.108173640.108173640_tile_1 ATM10.chr11.108173640.108173640_tile_1 1 chr11 108173612 108173801 + AAATCTGTGGATTCCTCTAAGTGAAAATCATGACATTTGGATAAAGACACTGACTTGTGCTTTTTTGGACAGTGGAGGCACAAAATGTGAAATTCTTCAATTATTAAAGCCAATGTGTGAAGTAAGAAGATTAATT Homo sapiens hg19 +ATM11.chr11.108180945.108180945_tile_1 ATM11.chr11.108180945.108180945_tile_1 1 chr11 108180915 108181101 + AAGTTGCCAAGGTAGCTCAGTCTTGTGCTGCTCACTTTACAGCTTTACTCTATGCAGAAATCTATGCAGATAAGAAAAGTATGGATGATCAAGAGAAAAGGTAATGGAATTTAGAATTTTTGGTTTTTAAAA Homo sapiens hg19 +ATM12.chr11.108200958.108200961_tile_1 ATM12.chr11.108200958.108200961_tile_1 1 chr11 108200926 108201096 + TTCAGCGAGAGCTGGAGTTGGATGAATTAGCCCTGCGTGCACTGAAAGAGGATCGTAAACGCTTCTTATGTAAAGCAGTTGAAAATTATATCAACTGCTTATTAAGTGGAGAAGA Homo sapiens hg19 +ATM14.chr11.108204681.108204681_tile_1 ATM14.chr11.108204681.108204681_tile_1 1 chr11 108204651 108204823 + TACTATGGAAATTAAGGTAATTTGCAATTAACTCTTGATTTTTTTTAAACTAAATTTTTTTTATTAGATTGAACCATTTGAAATAGTATTTTTATGTAGGTCAAAATTGGTTAAATA Homo sapiens hg19 +ATM15.chr11.108205769.108205769_tile_1 ATM15.chr11.108205769.108205769_tile_1 1 chr11 108205739 108205928 + AGGTGTAAATTTACCAAAAATAATAGATTGTGTAGGTTCCGATGGCAAGGAGAGGAGACAGCTTGTTAAGGTGAGCCTTCCCTTCTCTGGCTTAGCCCTTAGAGTTTTAGTGATGAAAATTTTTAGTTCATATT Homo sapiens hg19 +ATM16.chr11.108206594.108206594_tile_1 ATM16.chr11.108206594.108206594_tile_1 1 chr11 108206566 108206750 + GATGCTGTCATGCAACAGGTCTTCCAGATGTGTAATACATTACTGCAGAGAAACACGGAAACTAGGAAGAGGAAATTAACTATCTGTACTTATAAGGTAACTATTTGTACTTCTGTTAGTTCACCAAAAAC Homo sapiens hg19 +ATM17.chr11.108218089.108218089_tile_1 ATM17.chr11.108218089.108218089_tile_1 1 chr11 108218061 108218247 + TCTAGGTAAGTAATAAAATCTATGTATCTATTCTTTTTAGTAAATATTTGGTCATCATGGAATGTTGTTTGCCTACCAAGATATTACAAATATAAGAGACAGATAAATTGAAGCAGTAAATATTGGGTTTTTT Homo sapiens hg19 +ATM18.chr11.108225590.108225590_tile_1 ATM18.chr11.108225590.108225590_tile_1 1 chr11 108225562 108225751 + AACCATTGTAGAGGTAAAGTATTTTATAAGGAAGACTTTATTTTTTTTCTTACCAGGTAGACTGTGTATCTCATCAGGAAGTCACTGATGTGAAGAGCACTGCTTCATTTTAACATAGGGGGATGTGGCTGGGCAGC Homo sapiens hg19 +ATM19.chr11.108236086.108236203_tile_1 ATM19.chr11.108236086.108236203_tile_1 1 chr11 108236058 108236241 + ACGTGTCTTAATGAGACTACAAGAGAAACTGAAAGGAGTGGAAGAAGGCACTGTGCTCAGTGTTGGTGGACAAGTGAATTTGCTCATACAGCAGGCCATAGACCCCAAAAATCTCAGCCGACTTTTCCCAG Homo sapiens hg19 +KRAS1.chr12.25378562.25378562_tile_1 KRAS1.chr12.25378562.25378562_tile_1 1 chr12 25378532 25378717 + TTGCTGATGTTTCAATAAAAGGAATTCCATAACTTCTTGCTAAGTCCTGAGCCTGTTTTGTGTCTACTGTTCTAGAAGGCAAATCACATTTATTTCCTACTAGGACCATAGGTACATCTTCAGAGTCCTTA Homo sapiens hg19 +KRAS2.chr12.25380275.25380283_tile_1 KRAS2.chr12.25380275.25380283_tile_1 1 chr12 25380245 25380427 + CCTCTTGACCTGCTGTGTCGAGAATATCCAAGAGACAGGTTTCTCCATCAATTACTACTTGCTTCCTGTAGGAATCCTGAGAAGGGAGAAACACAGTCTGGATTATTACAGTGCACCTTTTACTTCAA Homo sapiens hg19 +KRAS7.chr12.25398255.25398285_tile_1 KRAS7.chr12.25398255.25398285_tile_1 1 chr12 25398225 25398414 + TGTATCGTCAAGGCACTCTTGCCTACGCCACCAGCTCCAACTACCACAAGTTTATATTCAGTCATTTTCAGCAGGCCTTATAATAAAAATAATGAAAATGTGACTATATTAGAACATGTCACACATAAGGTTA Homo sapiens hg19 +PTPN11_1.chr12.112888163.112888211_tile_1 PTPN11_1.chr12.112888163.112888211_tile_1 1 chr12 112888135 112888323 + TGGTGATTACTATGACCTGTATGGAGGGGAGAAATTTGCCACTTTGGCTGAGTTGGTCCAGTATTACATGGAACATCACGGGCAATTAAAAGAGAAGAATGGAGATGTCATTGAGCTTAAATATCCTCTGAACTGT Homo sapiens hg19 +PTPN11_10.chr12.112926884.112926888_tile_1 PTPN11_10.chr12.112926884.112926888_tile_1 1 chr12 112926856 112927032 + GGTCAGGGATGGTCCAGACAGAAGCACAGTACCGATTTATCTATATGGCGGTCCAGCATTATATTGAAACACTACAGCGCAGGATTGAAGAAGAGCAGGTACCAGCCTGAGGGCTGGCATGCGG Homo sapiens hg19 +HNF1A_1.chr12.121431413.121431414_tile_1 HNF1A_1.chr12.121431413.121431414_tile_1 1 chr12 121431385 121431558 + GTGGGGCCCAGCATCCCAGCAGATCCTGTTCCAGGCCTATGAGAGGCAGAAGAACCCTAGCAAGGAGGAGCGAGAGACGCTAGTGGAGGAGTGCAATAGGTACAACGGCGGGCGGGAAACAG Homo sapiens hg19 +HNF1A_3.chr12.121432070.121432070_tile_1 HNF1A_3.chr12.121432070.121432070_tile_1 1 chr12 121432042 121432221 + GCGCAAAGAAGAAGCCTTCCGGCACAAGCTGGCCATGGACACGTACAGCGGGCCCCCCCCAGGGCCAGGCCCGGGACCTGCGCTGCCCGCTCACAGCTCCCCTGGCCTGCCTCCACCTGCCCTCTCCCCC Homo sapiens hg19 +FLT3_1.chr13.28592620.28592653_tile_1 FLT3_1.chr13.28592620.28592653_tile_1 1 chr13 28592590 28592766 + CATAGTTGGAATCACTCATGATATCTCGAGCCAATCCAAAGTCACATATCTTCACCACTTTCCCGTGGGTGACAAGCACGTTCCTGGCGGCCAGGTCTCTGTGAACACACTGTCAAGAATGA Homo sapiens hg19 +FLT3_13.chr13.28602329.28602329_tile_1 FLT3_13.chr13.28602329.28602329_tile_1 1 chr13 28602295 28602464 + GTGTGCACGCCCCCAGCAGGTTCACAATATTCTCGTGGCTTCCCAGCTGGGTCATCATCTTGAGTTCTGACATGAGTGCCTCTCTTTCAGAGCTGTCTGCTTTTTCTGTCAAAGAA Homo sapiens hg19 +FLT3_14.chr13.28608244.28608341_tile_1 FLT3_14.chr13.28608244.28608341_tile_1 1 chr13 28608214 28608402 + ACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCATACCTAAATTGCTTCAGAGATGAAATGATGAGTCA Homo sapiens hg19 +FLT3_22.chr13.28610138.28610138_tile_1 FLT3_22.chr13.28610138.28610138_tile_1 1 chr13 28610098 28610267 - TATAGGAGTGAACCACTATGCCCAGCCAGTGAGCTTATTTCACACGTTCTTTTCTATAGGGAAACCTCAAGTGCTCGCAGAAGCATCGGCAAGTCAGGCGTCCTGTTTCTCGGATGG Homo sapiens hg19 +RB1_1.chr13.48919244.48919244_tile_1 RB1_1.chr13.48919244.48919244_tile_1 1 chr13 48919156 48919336 + ATTTACTTTTTTCTATTCTTTCCTTTGTAGTGTCCATAAATTCTTTAACTTACTAAAAGAAATTGATACCAGTACCAAAGTTGATAATGCTATGTCAAGACTGTTGAAGAAGTATGATGTATTG Homo sapiens hg19 +RB1_2.chr13.48923148.48923148_tile_1 RB1_2.chr13.48923148.48923148_tile_1 1 chr13 48923120 48923296 + TTATTAGCTAAAGGTAAGTTCATTATATTTATTAAATGCTAATATTTCAAATGTAATAATTAAATTGGCATTCCTTTGGACTAAATTCCCCAATTTTTATTGAGTAATGTACTCCTCCCTCAT Homo sapiens hg19 +RB1_3.chr13.48942685.48942685_tile_1 RB1_3.chr13.48942685.48942685_tile_1 1 chr13 48942655 48942826 + ACGAAAAAGTAACCTTGATGAAGAGGTGAATGTAATTCCTCCACACACTCCAGTTAGGTATGAATTTTCCTACTTTTAATTATATTATAATTTTGTTATTCATGGCTTTATAGTG Homo sapiens hg19 +RB1_4.chr13.48955538.48955550_tile_1 RB1_4.chr13.48955538.48955550_tile_1 1 chr13 48955504 48955684 + TAGAACGATGTGAACATCGAATCATGGAATCCCTTGCATGGCTCTCAGTAAGTAGCTAAATAATTGAAGAAATTCATTCATGTGCATATGGCTAACAAATTATTGTTAGTGAGAGGTGTTTCTTA Homo sapiens hg19 +RB1_6.chr13.49027168.49027168_tile_1 RB1_6.chr13.49027168.49027168_tile_1 1 chr13 49027112 49027288 + TTTGATCTTATTAAACAATCAAAGGACCGAGAAGGACCAACTGATCACCTTGAATCTGCTTGTCCTCTTAATCTTCCTCTCCAGAATAATCACACTGCAGCAGATATGTAAGCAAAATATA Homo sapiens hg19 +RB1_7.chr13.49033843.49033846_tile_1 RB1_7.chr13.49033843.49033846_tile_1 1 chr13 49033813 49033989 + TCTCCGGCTAAATACACTTTGTGAACGCCTTCTGTCTGAGCACCCAGAATTAGAACATATCATCTGGACCCTTTTCCAGCACACCCTGCAGAATGAGTATGAACTCATGAGAGACAGGCATTT Homo sapiens hg19 +RB1_8.chr13.49037877.49037877_tile_1 RB1_8.chr13.49037877.49037877_tile_1 1 chr13 49037815 49037985 + TTTACATCAATTTATTTACTAGATTATGATGTGTTCCATGTATGGCATATGCAAAGTGAAGAATATAGACCTTAAATTCAAAATCATTGTAACAGCATACAAGGATCTTCCTCA Homo sapiens hg19 +RB1_9.chr13.49039164.49039164_tile_1 RB1_9.chr13.49039164.49039164_tile_1 1 chr13 49039132 49039304 + AAGAGGAGTATGATTCTATTATAGTATTCTATAACTCGGTCTTCATGCAGAGACTGAAAACAAATATTTTGCAGTATGCTTCCACCAGGGTAGGTCAAAAGTATCCTTTGATTGGAAAA Homo sapiens hg19 +AKT1.chr14.105246455.105246455_tile_1 AKT1.chr14.105246455.105246455_tile_1 1 chr14 105246429 105246600 + CTCACGTTGGTCCACATCCTGCGGCCGCTCCTTGTAGCCAATGAAGGTGCCATCATTCTTGAGGAGGAAGTAGCGTGGCCGCCAGGTCTTGATGTACTCCCCTACAGACGTGCGGGTGGTGA Homo sapiens hg19 +CDH1_1.chr16.68835649.68835650_tile_1 CDH1_1.chr16.68835649.68835650_tile_1 1 chr16 68835613 68835782 + TGGGCACAGATGGTGTGATTACAGTCAAAAGGCCTCTACGGTTTCATAACCCACAGATCCATTTCTTGGTCTACGCCTGGGACTCCACCTACAGAAAGTTTTCCACCAAAGTCACGCTGAAT Homo sapiens hg19 +CDH1_2.chr16.68846137.68846137_tile_1 CDH1_2.chr16.68846137.68846137_tile_1 1 chr16 68846109 68846283 + CGATAATCCTCCGATCTTCAATCCCACCACGGTAATTCTATAACTCCTTAGAGGGTTTCCAAAGAAAGGTCTTTTGTTGTTCATGAACTAAGTGTCACCACTGCTCATGGGCGAAGTCTTT Homo sapiens hg19 +CDH1_3.chr16.68847274.68847277_tile_1 CDH1_3.chr16.68847274.68847277_tile_1 1 chr16 68847246 68847422 + ACTGATGCTGATGCCCCCAATACCCCAGCGTGGGAGGCTGTATACACCATATTGAATGATGATGGTGGACAATTTGTCGTCACCACAAATCCAGTGAACAACGATGGCATTTTGAAAACAGCA Homo sapiens hg19 +TP53_1.chr17.7574003.7574021_tile_1 TP53_1.chr17.7574003.7574021_tile_1 1 chr17 7573977 7574147 + CGGAACATCTCGAAGCGCTCACGCCCACGGATCTGCAGCAACAGAGGAGGGGGAGAAGTAAGTATATACACAGTACCTGAGTTAAAAGATGGTTCAAGTTACAATTGTTTGACTTTATG Homo sapiens hg19 +TP53_3.chr17.7577022.7577129_tile_1 TP53_3.chr17.7577022.7577129_tile_1 1 chr17 7576996 7577166 + CGCTTAGTGCTCCCTGGGGGCAGCTCGTGGTGAGGCTCCCCTTTCTTGCGGAGATTCTCTTCCTCTGTGCGCCGGTCTCTCCCAGGACAGGCACAAACACGCACCTCAAAGCTGTTCCG Homo sapiens hg19 +TP53_17.chr17.7577523.7577574_tile_1 TP53_17.chr17.7577523.7577574_tile_1 1 chr17 7577495 7577683 + GGTGAGGATGGGCCTCCGGTTCATGCCGCCCATGCAGGAACTGTTACACATGTAGTTGTAGTGGATGGTGGTACAGTCAGAGCCAACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_1 TP53_31_59.chr17.7578190.7578536_tile_1 1 chr17 7578064 7578234 + AGAAAGCCCCCCTACTGCTCACCTGGAGGGCCACTGACAACCACCCTTAACCCCTCCTCCCAGAGACCCCAGTTGCAAACCAGACCTCAGGCGGCTCATAGGGCACCACCACACTA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_2 TP53_31_59.chr17.7578190.7578536_tile_2 1 chr17 7578156 7578325 - CTGATTGCTCTTAGGTCTGGCCCCTCCTCAGCATCTTATCCGAGTGGAAGGAAATTTGCGTGTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCC Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_3 TP53_31_59.chr17.7578190.7578536_tile_3 1 chr17 7578246 7578415 + TGAGGAGGGGCCAGACCTAAGAGCAATCAGTGAGGAATCAGAGGCCTGGGGACCCTGGGCAACCAGCCCTGTCGTCTCTCCAGCCCCAGCTGCTCACCATCGCTATCTGAGCAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_4 TP53_31_59.chr17.7578190.7578536_tile_4 1 chr17 7578346 7578515 - GTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAGTCACAGCACATGACGGAGGTTGTGAGGCGCTGCCCCCACCATGAGCGCTGCTCAGATAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_5 TP53_31_59.chr17.7578190.7578536_tile_5 1 chr17 7578468 7578645 + CCCACAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTAGGAAGAGGAAGGAGACAGAGTTGAAAGTCAGGGCACAAGTGAACAGATAAAGCAACTGGA Homo sapiens hg19 +TP53_60.chr17.7579358.7579403_tile_1 TP53_60.chr17.7579358.7579403_tile_1 1 chr17 7579324 7579507 + GCCCAGACGGAAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGGACAGAAGATGACAGGGGCCAGGAGGGGGCTGGTGCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGCAGGGGCCACGGGGGGAGCAG Homo sapiens hg19 +TP53_64.chr17.7579882.7579882_tile_1 TP53_64.chr17.7579882.7579882_tile_1 1 chr17 7579852 7580032 + GCTCGACGCTAGGATCTGACTGCGGCTCCTCCATGGCAGTGACCCGGAAGGCAGTCTGGCTGCTGCAAGAGGAAAAGTGGGGATCCAGCATGAGACACTTCCAACCCTGGGTCACCTGGGCCTGCAG Homo sapiens hg19 +ERBB2_1.chr17.37880219.37880261_tile_1 ERBB2_1.chr17.37880219.37880261_tile_1 1 chr17 37880191 37880361 + TGTTGAGGGAAAACACATCCCCCAAAGCCAACAAAGAAATCTTAGACGTAAGCCCCTCCACCCTCTCCTGCTAGGAGGACAGGAAGGACCCCATGGCTGCAGGTCTGGGCTCTGGTCT Homo sapiens hg19 +ERBB2_4.chr17.37880993.37881012_tile_1 ERBB2_4.chr17.37880993.37881012_tile_1 1 chr17 37880963 37881151 + CGTGATGGCTGGTGTGGGCTCCCCATATGTCTCCCGCCTTCTGGGCATCTGCCTGACATCCACGGTGCAGCTGGTGACACAGCTTATGCCCTATGGCTGCCTCTTAGACCATGTCCGGGAAAACCGCGGACGCCTGGG Homo sapiens hg19 +ERBB2_13.chr17.37881332.37881440_tile_1 ERBB2_13.chr17.37881332.37881440_tile_1 1 chr17 37881298 37881482 + GCGGCTCGTACACAGGGACTTGGCCGCTCGGAACGTGCTGGTCAAGAGTCCCAACCATGTCAAAATTACAGACTTCGGGCTGGCTCGGCTGCTGGACATTGACGAGACAGAGTACCATGCAGATGGGGGCA Homo sapiens hg19 +SMAD4_1.chr18.48575169.48575170_tile_1 SMAD4_1.chr18.48575169.48575170_tile_1 1 chr18 48575131 48575301 + TTTGACTTAAAATGTGATAGTGTCTGTGTGAATCCATATCACTACGAACGAGTTGTATCACCTGGAATTGGTAAGTAGACTTTGCTTTCATCCTAAGAAACATAAAGGGAAA Homo sapiens hg19 +SMAD4_2.chr18.48581198.48581198_tile_1 SMAD4_2.chr18.48581198.48581198_tile_1 1 chr18 48581168 48581346 + AGGGACAGCCATCGTTGTCCACTGAAGGACATTCAATTCAAACCATCCAGCATCCACCAAGTAATCGTGCATCGACAGAGACATACAGCACCCCAGCTCTGTTAGCCCCATCTGAGTCTAATGC Homo sapiens hg19 +SMAD4_3.chr18.48584560.48584560_tile_1 SMAD4_3.chr18.48584560.48584560_tile_1 1 chr18 48584528 48584714 + GGGCCTCAGCCAGGACAGCAGCAGAATGGATTTACTGGTCAGCCAGCTACTTACCATCATAGTATGTACATACTTTAAAAAATCTTTTAAATAGTTGAGAAAAAAGTAGGCAGCCTTTATAAAAGCAAATTAAC Homo sapiens hg19 +SMAD4_4.chr18.48586262.48586262_tile_1 SMAD4_4.chr18.48586262.48586262_tile_1 1 chr18 48586234 48586416 + CCAGCCTCCCATTTCCAATCATCCTGGTAAGTGTATTTCAAAATTGATTTCCTGTATTTAGATTGATTTAGTGGTGATTGAAACGCACAAACACAGGCTTTAATGGAATTATGGGGTCACTTCTCAGAT Homo sapiens hg19 +SMAD4_5.chr18.48591826.48591919_tile_1 SMAD4_5.chr18.48591826.48591919_tile_1 1 chr18 48591796 48591982 + TTGAAATGGATGTTCAGGTAGGAGAGACATTTAAGGTTCCTTCAAGCTGCCCTATTGTTACTGTTGATGGATACGTGGACCCTTCTGGAGGAGATCGCTTTTGTTTGGGTCAACTCTCCAATGTCCACAGGAC Homo sapiens hg19 +SMAD4_11.chr18.48593405.48593405_tile_1 SMAD4_11.chr18.48593405.48593405_tile_1 1 chr18 48593377 48593547 + AAGGTGTGCAGTTGGAATGTAAAGGTGAAGGTGATGTTTGGGTCAGGTGCCTTAGTGACCACGCGGTCTTTGTACAGAGTTACTACTTAGACAGAGAAGCTGGGCGTGCACCTGGAGA Homo sapiens hg19 +SMAD4_12.chr18.48603032.48603094_tile_1 SMAD4_12.chr18.48603032.48603094_tile_1 1 chr18 48602998 48603168 + TGTCATCGACAGATGCAGCAGCAGGCGGCTACTGCACAAGCTGCAGCAGCTGCCCAGGCAGCAGCCGTGGCAGGAAACATCCCTGGCCCAGGATCAGTAGGTGGAATAGCTCCA Homo sapiens hg19 +SMAD4_15.chr18.48604668.48604754_tile_1 SMAD4_15.chr18.48604668.48604754_tile_1 1 chr18 48604638 48604808 + CGTCGCTTATGCATACTCAGGATGAGTTTTGTGAAAGGCTGGGGACCGGATTACCCAAGACAGAGCATCAAAGAAACACCTTGCTGGATTGAAATTCACTTACACCGGGCCCTCCAGC Homo sapiens hg19 +STK11_1.chr19.1207021.1207092_tile_1 STK11_1.chr19.1207021.1207092_tile_1 1 chr19 1206993 1207169 + CCAGCCGCGCCGCAAGCGGGCCAAGCTCATCGGCAAGTACCTGATGGGGGACCTGCTGGGGGAAGGCTCTTACGGCAAGGTGAAGGAGGTGCTGGACTCGGAGACGCTGTGCAGGAGGGCCGT Homo sapiens hg19 +STK11_4.chr19.1220487.1220502_tile_1 STK11_4.chr19.1220487.1220502_tile_1 1 chr19 1220459 1220638 + CCGACCTGGGCGTGGCCGAGGTAGGCACGTGCTAGGGGGGGCCCTGGGGCGCCCCCTCCCGGGCACTCCCTGAGGGCTGCACGGCACCGCCACAGGCACTGCACCCGTTCGCGGCGGACGACACCTGCCG Homo sapiens hg19 +STK11_8.chr19.1221264.1221319_tile_1 STK11_8.chr19.1221264.1221319_tile_1 1 chr19 1221232 1221407 - CCCGCCTCCCTGGGGCTGCGGGCAGAGGGATGAGGCTCCCACCTTTCAGCAGGTCAGAGAGCGGGGGGCCACAGTCGCCCGGGATGGCGTAGCTCCCCTTCCCGATGTTCTCAAACAACTTG Homo sapiens hg19 +STK11_12.chr19.1223059.1223125_tile_1 STK11_12.chr19.1223059.1223125_tile_1 1 chr19 1223035 1223221 + GGCGCAGCATGACTGTGGTGCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACATCATCTACACTCAGGACTTCACGGTGCCCGGTGAGTCTGGCGGGGGCCCCTGCCC Homo sapiens hg19 +JAK3_1.chr19.17945696.17945696_tile_1 JAK3_1.chr19.17945696.17945696_tile_1 1 chr19 17945666 17945840 + GGTGACGCCACTAAACACTTCCCAGACCGTGGCGCCGAAGCCCCACTTGTCAGCTTCCAAGCTAAGTGTCTGCGCCTCCCGGAGACACTCGGGGGCCACCCAGGGGATCCTGTCGGTGAGCAC Homo sapiens hg19 +JAK3_2.chr19.17948009.17948009_tile_1 JAK3_2.chr19.17948009.17948009_tile_1 1 chr19 17947981 17948169 + CGCTGCTTCCAGGAATGACTGGGGAAGGTGGGAAGGGAGAGAAGATGCGTGGGTTTCTTCCACTCCAATAATCCCAAATTTTGTGCTCACAGACCTGCCTTAGGGGAACACCTGGCCACAGGTCACCTTTGGCCCTGG Homo sapiens hg19 +SRC.chr20.36031762.36031762_tile_1 SRC.chr20.36031762.36031762_tile_1 1 chr20 36031734 36031923 + CCAGCCCGGGGAGAACCTCTAGGCACAGGCGGGCCCAGACCGGCTTCTCGGCTTGGATCCTGGGCTGGGTGGCCCCTGTCTCGGGGCTTGCCCCACTCTGCCTGCCTGCTGTTGGTCCTCTCTCTGTGGGGCTGA Homo sapiens hg19 +GNAS1.chr20.57484420.57484421_tile_1 GNAS1.chr20.57484420.57484421_tile_1 1 chr20 57484390 57484560 + TGCCGTGTCCTGACTTCTGGAATCTTTGAGACCAAGTTCCAGGTGGACAAAGTCAACTTCCAGTAAGCCAACTGTTACCTTTTTATATAACAGAGATCATGGTTTCTTGACATTCAC Homo sapiens hg19 +SMARCB1_1.chr22.24133967.24133990_tile_1 SMARCB1_1.chr22.24133967.24133990_tile_1 1 chr22 24133939 24134126 + TCCGAGGTTCTCTGTACAAGAGATACCCCTCACTCTGGAGGCGACTAGCCACTGTGGAAGAGAGGAAGAAAATAGTTGCATCGTCACATGGTAAAAAAACAAAACCTAACACTAAGGGTGCGTCTTCACGAGGGTT Homo sapiens hg19 +SMARCB1_3.chr22.24143240.24143240_tile_1 SMARCB1_3.chr22.24143240.24143240_tile_1 1 chr22 24143210 24143383 + GGGCCGAGACAAGAAGAGAACCTTCCCCCTTTGGTGTGGATGCATCGCTGCACTCACCCTCCGTGCTGATTCCGCCTTAGTTCTCCAGCACGTTTCAGTTCCTTCCTCCCCAGAAAAACACT Homo sapiens hg19 +SMARCB1_4.chr22.24145582.24145582_tile_1 SMARCB1_4.chr22.24145582.24145582_tile_1 1 chr22 24145552 24145726 + GCTGCGAGACGCCTTCACCTGGAACATGAATGGTACAAGGCAGTCGGGCTTGGCTGGGCCTGGCCCCAACCCCTGTGTGTTACGTGGGAACAGTCCCGTTTCCTGCCAGCTGCCTGTCAGGC Homo sapiens hg19 +SMARCB1_5_6.chr22.24176352.24176357_tile_1 SMARCB1_5_6.chr22.24176352.24176357_tile_1 1 chr22 24176324 24176495 + CGGCCCCGGCCTGGTAACCAGCCCATCAGCACACGGCTCCCACGGAGCATCTCAGAAGATTGGGCCGCCTCTCCTCCATCTTCTGGCAAGGACAGAGGCGAGGGGACAGCCCAGCGCCA Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_1 GNA11_4.chr19.3114942.3115070_tile_1 1 chr19 3114824 3115004 - GTAGCCCAAGGTGGCGATGCGGTCAACGTCGGTCAGGTAGCTGCAACACAGCGGTGGGTGCTCAGGCCGGCTGCCGGGGGTGGGGGGGCAGGACAGGGACACAGCACCCAAACCAGCGGGAGGACGGAAAGCCACC Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_2 GNA11_4.chr19.3114942.3115070_tile_2 1 chr19 3114958 3115133 + CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCATCATCGAGTACCCTTTCGACCTGGAGAACATCATCTTCCGGTACCGCCCGGGCCACAGCAGGCGGGGAGGGGGCACTGAGA Homo sapiens hg19 +GNA11_5.chr19.3118922.3119051_tile_1 GNA11_5.chr19.3118922.3119051_tile_1 1 chr19 3118802 3118989 - CACTTCCTCCGCTCCGACCGCTGGCCCCCCACATCCACCATCCTGAAAGGACACAGCGCCAGGACTCAGCCACCTGGCGCCCCAAGGCCCAATCTGCAATCCCAGGACGGCTCCCACCCAAGCCCCTCCTGCCACACC Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_6.chr19.3119204.3119357_tile_2 1 chr19 3119208 3119395 - CCGCAGCCCGGCGCACCATCGAACTCGGGGAAGTAGTCCACCAGGTGCGAGTACAGGATCTTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGAGGATGACGGAGGAGTTCTGGAACCAGGGGTAGGTGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_7.chr19.3120987.3121177_tile_1 1 chr19 3120865 3121035 + GGGCCTTACTCGCTCATCCCCTGGGAGTGACAAAGGGGCCCACGAGTCCCTTGCCCTGGGCCGGGCTGGGGCACAGCCTCACCCTCTGCCCTCCCCCAGGTCCCCAGCGGGACGCCCAGGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 1 chr19 3120985 3121170 - CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTCCGTGTCGGTGGCACACGTGAAGTGTGAGTAGATGATCTTGTCGCTGTCGGGGTTCAGGTCCACGAACATCTTCAGGATGAACTCCCGCGCCGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_3 GNA11_7.chr19.3120987.3121177_tile_3 1 chr19 3121121 3121304 + GCAGCTCAACCTCAAGGAGTACAACCTGGTCTGAGCGCCCAGGCCCAGGGAGACGGGATGGAGACACGGGGCAGGACCTTCCTTCCACGGAGCCTGCGGCTGCCGGGCGGGTGGCGCTGCCGAGTCCGGGCCGGGGC Homo sapiens hg19 +GNAQ_4.chr9.80412436.80412564_tile_1 GNAQ_4.chr9.80412436.80412564_tile_1 1 chr9 80412406 80412592 + TACCTGAAAATGACACTTTGTAAGTCAAAGGGGTATTCGATGATCCCTGTGGTGGGGACTCGAACTCTAAGCACATCTTGTTGCGTAGGCAGGTAGGCAGGGTCAGCTACGCGGTCCAAGTCATTAAGATAGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_5.chr9.80409379.80409508_tile_1 1 chr9 80409249 80409421 + AAAGAAGTAAGTTCACTCCATTCCCCACACCCTACTTTCTATCATTTACTTGTATCAGATAATAAAATGATAATCCATTGCCTGTCTAAAGAACACTTACCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 1 chr9 80409335 80409510 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCAAGTTCTCGTGGAGTCAGACAATGAGGTAAGTGTTCTTTA Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_3 GNAQ_5.chr9.80409379.80409508_tile_3 1 chr9 80409459 80409639 + TTTGGCCCCCTACATCGACCATTCTGCAAGGTTAACAATACTCATATTAATAACATATAAAGTAAAACTAAAAAGTCAACATAAATATAGCACTACTTACAAACTTAGGGAAAATATTCTCTTGAAT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_6.chr9.80343430.80343583_tile_1 1 chr9 80343306 80343476 + GGGCAGCAATGGTGCACTGTAGTGCGTTAACTCCCACACTGGGGTTTGGAGACAAAACCTATTCACAGCTACTGAGCTGTGGTATGAGTGCTGACTTACCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_2 GNAQ_6.chr9.80343430.80343583_tile_2 1 chr9 80343392 80343561 - GGTTCCAGAACTCCTCGGTTATTCTGTTCTTAAACAAGAAAGATCTTCTAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGTAAGTCAGCAC Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_3 GNAQ_6.chr9.80343430.80343583_tile_3 1 chr9 80343504 80343689 + CAGGGGTATGTGATAATTGTTCTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTGGAAAAAAAAAAAAAATCAGAAAAAACAAGGAGTGAATTACATGATTACTTAATTTGTGAATTGTGTTTATTTT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 1 chr9 80336110 80336280 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCAGGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAATTAGACCAGATTGTACT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_7.chr9.80336240.80336429_tile_2 1 chr9 80336204 80336374 - CTACTCCCACTTCACGTGCGCCACAGACACCGAGAATATCCGCTTTGTCTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGAGTACAATCTGGTCTAATTGTGCCTCC Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_3 GNAQ_7.chr9.80336240.80336429_tile_3 1 chr9 80336320 80336495 + GATAATTTTGTCACTGTCTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCTTTCGGCCAAGAGACAAGAGGGACACTTTGTTACCTA Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 2 chr22 17052964 17053133 + ATCCTCTCTCTGAAATCACTGCGCAGGAGAAAGATTTTCTATGGACCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGACTTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 2 chr22 17055413 17055585 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTGTCAAACAGGAGAAGAAGGATGAAACACAAAAGTTGTGTGACTCTAGTCTGTGTTTGAGACTCTT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN3.chr10.89685307.89685307_tile_1 2 chr9 33675957 33676480 - ATACACAATCTTTGTGCTGAAAGACATTATGACACCGCCAAATCTAATTACAGAGTTGCGCAATATCCTTTTGAAGACCATAACCCACCACAGCTAGAACTTATCAAACCCTTTTGTGAAGATCTTGACCAATGGCTAAGTGAAGATGACAATCATGTTGCAGCAATTCACTGTAAAGCTGGAAAGGGACGAACTGGTATAATGATTTATGCATATTTATTACATCGGGGCAAATTTTTAAAGGCACAAGAGGCCCTAGATTTCTATGGGGAAGTAAGGACCAGAGACAAAAAGGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTACTATAGCTACCTGGTAAAGAATCATGTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 2 chr9 33675629 33675815 - CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATTGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAGTATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 2 chr7 65970150 65970483 + CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTTCGTGTCGGTGGCGTACGTGAAGTGGGAGTCGATGATCTTGTCGCTGTCGGGGTTCATGTCCACTAACATCTTCAGGATGAACTCCCGCGCCGCCTGGGCGTCCTGCTGGGGCCCTTCGAACTCGGGGAAGTAGTCCACCATGTGTGAGTACAGGATATTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGGTGATGACGGGGGAGTTCTGGAACCAGGGGTAGTCGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_4.chr19.3114942.3115070_tile_2 2 chr7 65970285 65970719 - CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCGTCTTTCGACCTGGAGAACATCATCTTCAGGATGGCGGATGTTGGGGGACAGCGGTCGGCGCAGAGGAAGTGGATCCACTGCTTTGAGAACCTGACGTCCATCCCGTTTCTCGTCGCCCTCAGTGAATACGACCAAGTCCTGGTGGAGTCGGACAACGAGAACCGGATGGAGGAGAGCAAAGCCCTGTTCCGGACCATCATCGACTACCCCTGGTTCCAGAACTCCCCCGTCATCACCTTCCTCAACAAGAAGGACCTGCTGGAGGACAATATCCTGTACTCACACATGGTGGACTACTTCCCCGAGTTCGAAGGGCCCCAGCAGGACGCCCAGGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 2 chr2 132181238 132181750 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCATGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAACTAGACCAGATTGTAATCCTTCAGGTTCAACTGGAGGATGGTGTCCTTGACGGCAGCAAACACAAAGCGGATATTCTCGGTGTCTGTGGCGCATGTGAAGTGGGAGTAGATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGTAGTCGACTAGATGGGAATACATGATTTTCTCCTCTGGAAGATCTTTCTTGTTTAACAACAGAATAACCGAGGAGTTCTGGAACCAGGGATACGTGATAATTGTACTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_7.chr9.80336240.80336429_tile_3 2 chr2 132181448 132181600 + GATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 2 chr2 132181332 132181839 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCGAGTTCTCGTGGAGTCAGACAATGAGAACCGAATGGAGGAAAGCAAGGCTCTCTTTAGTACAATTATCACGTATCCCTGGTTCCAGAACTCCTCGGTTATTCTGTTGTTAAACAAGAAAGATCTTCCAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGACCCCAGAGAGATGCCCAGGCAGCCCGAGAATTCATTCTGAAGATGTTCGTGGACCTGAACCCAGTGACCAAATTATCTACTCCCACTTCACATGCGCCACAGACACCGAGAATATCCGCTTTGTGTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGATTACAATCTGGTCTAGTTGTGCCTCC Homo sapiens hg19
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/TruSeq_Custom_Amplicon_Control_Manifest_ACP1.txt Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,695 @@ +[Header] +Customer Name Illumina +Product Type 15025138 +Date Manufactured +Lot +DesignStudio ID TSCA_Control +Target Plexity 341 + +[Probes] +Target Region Name Target Region ID Target ID Species Build ID Chromosome Start Position End Position Submitted Target Region Strand ULSO Sequence ULSO Genomic Hits DLSO Sequence DLSO Genomic Hits Probe Strand Designer Design Score Expected Amplifed Region Size SNP Masking Labels +snp_rs10138962 snp_rs10138962 snp_rs10138962 Homo sapiens hg19 chr14 104995819 104995868 + AAGCCAAGAACCCTCTCAGGCT 282 TGCGCACCTGTGGTCCCAGCTACTCA 1200 + ILLUMINA 5.13E-61 191 FALSE ACP1 +snp_rs1149580 snp_rs1149580 snp_rs1149580 Homo sapiens hg19 chr11 76549431 76549489 + GGATCAATGAACAGGTTATACAGGCTG 32 ACTGGGGACAAAGGGATAAACTAGACC 68 + ILLUMINA 0.817486141 200 FALSE ACP1 +snp_rs10988298 snp_rs10988298 snp_rs10988298 Homo sapiens hg19 chr9 132042416 132042471 + GAGGCTGAGATGGGAGGATCACTTGAA 1200 ATTGTGCACCCTCCATACAAATGTATG 75 + ILLUMINA 2.84E-58 197 FALSE ACP1 +snp_rs10086550 snp_rs10086550 snp_rs10086550 Homo sapiens hg19 chr8 143362946 143363004 + GTGTGACTACAGTGGGAAGAGGACAT 51 CATAGAGGAAGGGCTGTGGCCCA 73 + ILLUMINA 0.38673505 200 FALSE ACP1 +snp_rs10409978 snp_rs10409978 snp_rs10409978 Homo sapiens hg19 chr19 57796594 57796646 + TGTCTTACTTAGAAAGGGTTGGCTACG 50 TTATGGGTCTGCTCCTGTCACTGTCTT 115 + ILLUMINA 0.584760563 194 FALSE ACP1 +snp_rs1060493 snp_rs1060493 snp_rs1060493 Homo sapiens hg19 chr15 31516370 31516476 + AAACCCTCTGCTGGGACCGCCAA 23 TGAGGAGCCGTGGGGCTCACGTTTCA 12 + ILLUMINA 0.070951385 248 FALSE ACP1 +snp_rs12777222 snp_rs12777222 snp_rs12777222 Homo sapiens hg19 chr10 35387873 35387930 + TAGTGAGTTGAGATTGCATCATTGCAC 1163 GAACAAATGGACTAAAAGACGTAGTTCC 47 + ILLUMINA 1.21E-54 199 FALSE ACP1 +snp_rs12563211 snp_rs12563211 snp_rs12563211 Homo sapiens hg19 chr1 34486119 34486219 + TCAGGCAGCAACAACGCCCTGAGCAA 19 AAATTGTGCATGACCTTTAGGTCCTGG 47 + ILLUMINA 0.272884262 242 FALSE ACP1 +snp_rs10843013 snp_rs10843013 snp_rs10843013 Homo sapiens hg19 chr12 28025101 28025174 + ACTAATCCTACCCTTAAGGCTTTCTTT 41 ATCACAGCTCCATATATGCCTTGTGTG 47 + ILLUMINA 0.646311699 215 FALSE ACP1 +snp_rs12678837 snp_rs12678837 snp_rs12678837 Homo sapiens hg19 chr8 22950305 22950356 + GCAGTCCAGCTCTGATGGAGCTGTCA 53 TGCATCCTCATCAGTGGGCCCAGGTT 46 + ILLUMINA 0.608241088 193 FALSE ACP1 +snp_rs10954737 snp_rs10954737 snp_rs10954737 Homo sapiens hg19 chr7 83532935 83533038 + GAGGCAGCTTGTAAGTTATAAGAAATC 35 AAAACTGTTTTGAAGGGCTCAAGCCC 66 + ILLUMINA 0.265474762 245 FALSE ACP1 +snp_rs11100509 snp_rs11100509 snp_rs11100509 Homo sapiens hg19 chr4 164478785 164478875 + CACATTCTAGAACAGTTCCCATTTTTC 105 AAATCTTCATGTTGAATACTTTTTCACTG 261 + ILLUMINA 0.002100139 232 FALSE ACP1 +snp_rs12636227 snp_rs12636227 snp_rs12636227 Homo sapiens hg19 chr3 65065386 65065482 + CATTTGTGGAAGCAAGGCATCCTTCT 53 AAAACCACAGGACTTAGGGCAAAATGG 61 + ILLUMINA 0.398397766 238 FALSE ACP1 +snp_rs10038337 snp_rs10038337 snp_rs10038337 Homo sapiens hg19 chr5 11512340 11512425 + CAACACAGTGTTTGCTTTAATGCTCTG 165 ATCTAGGCAGTTAGGATGTCCATTAAC 49 + ILLUMINA 0.091055737 227 FALSE ACP1 +snp_rs10509415 snp_rs10509415 snp_rs10509415 Homo sapiens hg19 chr10 82472980 82473063 + AATAGTGGGGAAATCATCTTGCCTCAG 59 TCTATGGATTTATAGAGGAGTAGAAGAGG 166 + ILLUMINA 0.114550875 225 FALSE ACP1 +snp_rs10757399 snp_rs10757399 snp_rs10757399 Homo sapiens hg19 chr9 23186370 23186421 + GCCATCGTACAGCTAAATTTGTAAGTGG 28 TGGGAGTTTTGAACATATTTTAGGCAA 240 + ILLUMINA 0.01822009 193 FALSE ACP1 +snp_rs10919337 snp_rs10919337 snp_rs10919337 Homo sapiens hg19 chr1 170216910 170216970 + GAAGCATTTAATGAAATAAAGCAGAGAAG 533 TTTAAAGGAAGCTGCCCAGAACTGC 91 + ILLUMINA 3.17E-11 202 FALSE ACP1 +snp_rs11205541 snp_rs11205541 snp_rs11205541 Homo sapiens hg19 chr1 49254315 49254404 + GTGAAACACAGTGTTCTCAATCATAAA 68 TTTACTATTGAACTATTTGGTGAGCGC 56 + ILLUMINA 0.366528454 231 FALSE ACP1 +snp_rs10819072 snp_rs10819072 snp_rs10819072 Homo sapiens hg19 chr9 101361505 101361553 + TCCAACCTAGGGGCTTCAAACTCAGTT 38 GGAAGGTTCTGTAGACAAGCAGAACA 52 + ILLUMINA 0.905035471 190 FALSE ACP1 +snp_rs1078814 snp_rs1078814 snp_rs1078814 Homo sapiens hg19 chr3 193732947 193733001 + TTTATGCCGATTTTACTGGCCTCGTTG 17 GATAGCTCCCATGGATGGTGAGTGAAA 76 + ILLUMINA 0.746851007 196 FALSE ACP1 +snp_rs10487657 snp_rs10487657 snp_rs10487657 Homo sapiens hg19 chr7 82713031 82713144 + TGGTAAATGAGTCTGTTTCCTATTAGTG 74 ACATTTAATTCTCATTTGGCATTTGTAAG 210 + ILLUMINA 0.009085148 255 FALSE ACP1 +snp_rs10930331 snp_rs10930331 snp_rs10930331 Homo sapiens hg19 chr2 151750556 151750607 + GTAGTATGACTTAAGTGAGAGAGGAAG 54 CTGCATTATTAGCTATACAGCAAACAG 69 + ILLUMINA 0.755023344 193 FALSE ACP1 +snp_rs11075329 snp_rs11075329 snp_rs11075329 Homo sapiens hg19 chr16 17123751 17123840 + CTCAGTGGTTTGGCATAATGGAAATTC 56 AAGAAGGAGCTGGCATTCAAGTCTTG 100 + ILLUMINA 0.363982947 231 FALSE ACP1 +snp_rs10050438 snp_rs10050438 snp_rs10050438 Homo sapiens hg19 chr5 10139056 10139128 + TAGGAGGATCTGCCTGACCCAAATGA 43 AGGTGATCCGGCACCCGCAAATTCAGA 36 + ILLUMINA 0.590150376 214 FALSE ACP1 +snp_rs10425564 snp_rs10425564 snp_rs10425564 Homo sapiens hg19 chr19 57312898 57312973 + GTGCGGAAATAGAGATGTTTGCTGTAC 43 AAAATACCTCTGCTCTCAAAAGGGCA 84 + ILLUMINA 0.502413289 217 FALSE ACP1 +snp_rs11266838 snp_rs11266838 snp_rs11266838 Homo sapiens hg19 chr7 126792754 126792832 + AAGGTCAGCCTAGTGTCCTTAGGTGA 27 TTTCAGACATGTTTCATAGGACTACAG 51 + ILLUMINA 0.449172653 220 FALSE ACP1 +snp_rs10870311 snp_rs10870311 snp_rs10870311 Homo sapiens hg19 chr10 134290435 134290493 + ATTAATCAGCCCAACCTTTGCATCTGC 49 TTGCAGGACTCATGGTGCAGGGT 45 + ILLUMINA 0.503025892 200 FALSE ACP1 +snp_rs10993058 snp_rs10993058 snp_rs10993058 Homo sapiens hg19 chr9 96873061 96873137 + TAACCTGGCAAAGCTGCCCGTCAAAGT 52 AGGAAGTACATGATTTCTTGCCACTGT 76 + ILLUMINA 0.580524574 218 FALSE ACP1 +snp_rs10972175 snp_rs10972175 snp_rs10972175 Homo sapiens hg19 chr9 34625323 34625384 + GCTCTGACATTCCTGGAAAGGAATTTC 99 GACCCTGGACACAGAACCAAGGCATT 92 + ILLUMINA 0.510432046 203 FALSE ACP1 +snp_rs11582151 snp_rs11582151 snp_rs11582151 Homo sapiens hg19 chr1 37796519 37796576 + GCAAGATGGGTCACCAGCAGCTCTACT 60 AGTAGATTAGCCAAGGCACCCACTCAA 30 + ILLUMINA 0.745283701 199 FALSE ACP1 +snp_rs11085825 snp_rs11085825 snp_rs11085825 Homo sapiens hg19 chr19 13007357 13007445 + CTTTGTCAGGCAGGCTCCGTGCT 47 TCAGCCTCCTGGCTCTGAGCATCGAA 71 + ILLUMINA 0.187309361 230 FALSE ACP1 +snp_rs10246620 snp_rs10246620 snp_rs10246620 Homo sapiens hg19 chr7 43424032 43424089 + AGCCCCAGGAACACCTCTGGAGGGAAT 74 AAAAATACGTCTTTGCCTAAAACTTAAAC 94 + ILLUMINA 0.32864177 199 FALSE ACP1 +snp_rs11045044 snp_rs11045044 snp_rs11045044 Homo sapiens hg19 chr12 20257796 20257887 + TGAAAACCCATCCATTGACCCATTTATC 77 CACTCTCATTCGTATACTTTAGACTTGTG 39 + ILLUMINA 0.314654098 233 FALSE ACP1 +snp_rs10189240 snp_rs10189240 snp_rs10189240 Homo sapiens hg19 chr2 144484408 144484483 + ACCTAACCAAGTATCTGTACCTCCACA 37 ATAAATCTCAGCTTGGGATCCACAGAC 82 + ILLUMINA 0.583256128 217 FALSE ACP1 +snp_rs11008285 snp_rs11008285 snp_rs11008285 Homo sapiens hg19 chr10 31130903 31130970 + ACTCCAGCCTGGATGACAGAGCAAGA 1200 TTCTCCCAAGTCTGGCCAAAAGCCTAA 67 + ILLUMINA 2.40E-58 209 FALSE ACP1 +snp_rs11139732 snp_rs11139732 snp_rs11139732 Homo sapiens hg19 chr9 85365424 85365500 + TCTGATGGAGATCTTATTCTCCCAGAG 54 AATCTGGAGTCCATTTTGCCCATGCA 44 + ILLUMINA 0.55328873 218 FALSE ACP1 +snp_rs10736719 snp_rs10736719 snp_rs10736719 Homo sapiens hg19 chr11 61999654 61999714 + CTTAGAAGCCCAAATTAAGTTCAGAAAC 70 CTCTGAATGAGGATTTGGTTCATAGGG 44 + ILLUMINA 0.669444255 202 FALSE ACP1 +snp_rs10891556 snp_rs10891556 snp_rs10891556 Homo sapiens hg19 chr11 113352679 113352753 + TGTTCCACACTGCAAAACAATGCTGC 57 ATCAATGAGGTTTGGAAAGGGTGGCA 84 + ILLUMINA 0.510725191 216 FALSE ACP1 +snp_rs10741165 snp_rs10741165 snp_rs10741165 Homo sapiens hg19 chr10 130610943 130611010 + TGAAATTCAACAATTTCCTTCGAAAGC 110 ATCCTGAGAATAATAGTAAGAGCGGCC 43 + ILLUMINA 0.412482229 209 FALSE ACP1 +snp_rs1055273 snp_rs1055273 snp_rs1055273 Homo sapiens hg19 chr16 58028857 58028938 + AAGAATTAGCAGTTGGGACGGTTGTAG 27 TCAGGGCCCTTGGTGTGCCCACTGATTA 50 + ILLUMINA 0.469236873 223 FALSE ACP1 +snp_rs10740396 snp_rs10740396 snp_rs10740396 Homo sapiens hg19 chr10 74019951 74020035 + GATCCTGTTCCATGTGGCAAGAGCTT 55 AAGAGGCAAATAGGTATGTAGGTCAGC 53 + ILLUMINA 0.545209534 226 FALSE ACP1 +snp_rs10112900 snp_rs10112900 snp_rs10112900 Homo sapiens hg19 chr8 19646421 19646483 + GATGACTGTATTTGGAAGGTAGTTCAG 53 TAATCTCCCTGAAAACGGACCATTACA 47 + ILLUMINA 0.75040328 204 FALSE ACP1 +snp_rs10422772 snp_rs10422772 snp_rs10422772 Homo sapiens hg19 chr19 9723318 9723425 + AACTCTTCACAAAACCCCACTGCCT 71 TTATTATTATGCAGGGTGGTTTGAGAC 66 + ILLUMINA 0.202458701 249 FALSE ACP1 +snp_rs11002468 snp_rs11002468 snp_rs11002468 Homo sapiens hg19 chr10 80011963 80012029 + TCTCCAAGCATGGCTCCCATCTGGTTA 57 TGTGCCCATAGGCACCTCCTGGGAAT 59 + ILLUMINA 0.642689469 208 FALSE ACP1 +snp_rs11044070 snp_rs11044070 snp_rs11044070 Homo sapiens hg19 chr12 18546143 18546219 + CATGGTAACTCCCTTTAAATATCAGAGG 61 ATAGATGGAGAACAGCCTTCAATGTGG 67 + ILLUMINA 0.613806499 218 FALSE ACP1 +snp_rs10139797 snp_rs10139797 snp_rs10139797 Homo sapiens hg19 chr14 101708517 101708578 + AGATCCTGACCATGGAAGAATCAGAGG 59 GATGACCCAGTGAATGCGGGGCACA 27 + ILLUMINA 0.570836291 203 FALSE ACP1 +snp_rs10825371 snp_rs10825371 snp_rs10825371 Homo sapiens hg19 chr10 56435269 56435346 + AATTCTAAGGCCTTTTCATGTTGTTTT 120 ACTTCCTCCCCCAAGTATAGGTCAAA 38 + ILLUMINA 0.216134472 219 FALSE ACP1 +snp_rs11017755 snp_rs11017755 snp_rs11017755 Homo sapiens hg19 chr10 132944089 132944152 + CCTTGTAGCCAGGCATCTCTGCCTCT 54 GTTCCTCTCTGTTTCTTGGCGAAACA 54 + ILLUMINA 0.62682178 205 FALSE ACP1 +snp_rs11134290 snp_rs11134290 snp_rs11134290 Homo sapiens hg19 chr5 8202447 8202503 + ATGATGATACTCAGCCCAAGGGAGCT 39 CAAATCCCATTAGGGGCTTTGGACAT 42 + ILLUMINA 0.78115378 198 FALSE ACP1 +snp_rs10803015 snp_rs10803015 snp_rs10803015 Homo sapiens hg19 chr1 242243096 242243148 + CTGACCTCTGGTGATCCACCTGCCTA 1200 GGCAATGAGAGTTGTCCTCTCTGTGT 65 + ILLUMINA 2.63E-58 194 FALSE ACP1 +snp_rs1038074 snp_rs1038074 snp_rs1038074 Homo sapiens hg19 chr5 150358860 150358935 + AAGCGCGCAGTTATGTTTCTATAGAAA 58 GATATGAATGTTACTATATGTGCCACTAC 61 + ILLUMINA 0.485826376 217 FALSE ACP1 +snp_rs10207380 snp_rs10207380 snp_rs10207380 Homo sapiens hg19 chr2 241860797 241860881 + CATTGTTGCTGGCACCCCTGGGA 23 CACAGAAATGCTGCCGACAGATTAGT 28 + ILLUMINA 0.159512362 226 FALSE ACP1 +snp_rs10235210 snp_rs10235210 snp_rs10235210 Homo sapiens hg19 chr7 116003359 116003415 + ACTCTTTATGGGCAAAAATTTATTCTTTC 196 ATATGCTCTTCACAGGAGTTTCCACTC 66 + ILLUMINA 0.062074325 198 FALSE ACP1 +snp_rs10185490 snp_rs10185490 snp_rs10185490 Homo sapiens hg19 chr2 71166760 71166812 + GGAGGTAGGGGCGGCAGTGTACAAACAA 44 ATCCCTCTAGGGTCCCAGTCTGTAGTA 39 + ILLUMINA 0.731156187 194 FALSE ACP1 +snp_rs10109406 snp_rs10109406 snp_rs10109406 Homo sapiens hg19 chr8 72632603 72632656 + GCACTGGCTATATCTCCACTCCTTTCT 35 TACAGATGCCCCCATGGTGGGATCTTA 31 + ILLUMINA 0.833771305 195 FALSE ACP1 +snp_rs10095650 snp_rs10095650 snp_rs10095650 Homo sapiens hg19 chr8 82918286 82918381 + GAATCCATATTAAATGACAGTATCCTGTC 89 TTCTCCTGAGAGGTGACTGTGATATCG 56 + ILLUMINA 0.299972573 237 FALSE ACP1 +snp_rs10840020 snp_rs10840020 snp_rs10840020 Homo sapiens hg19 chr11 8339791 8339873 + AATGGCCTACAGTTGCCAAATTTTGT 50 AAACCTCATTCCCAGAGGGTCAAGCAT 63 + ILLUMINA 0.502325149 224 FALSE ACP1 +snp_rs10502584 snp_rs10502584 snp_rs10502584 Homo sapiens hg19 chr18 29797390 29797460 + GAAAAAGTCCTCATAACAGTCCAGTCA 43 TGTTTTAGTATCAGATTAGGAGGAATTCC 69 + ILLUMINA 0.547938278 212 FALSE ACP1 +snp_rs10106093 snp_rs10106093 snp_rs10106093 Homo sapiens hg19 chr8 29355343 29355403 + GGAGGAGAGACAGCATCTCCTCTGT 68 GAGAATTAAGCTCTGTGGTCAGACTCT 60 + ILLUMINA 0.681295961 202 FALSE ACP1 +snp_rs10832136 snp_rs10832136 snp_rs10832136 Homo sapiens hg19 chr11 13925649 13925709 + TTAATGTGACTACTAGAGTGGCATACGC 44 TTGTCGTCTTTGGTAGTGGGCATGGAA 60 + ILLUMINA 0.81035586 202 FALSE ACP1 +snp_rs1028530 snp_rs1028530 snp_rs1028530 Homo sapiens hg19 chr14 27441076 27441125 + TCATTGCAATAGAATATTAATAGGCGATG 140 TGTGCACGATGGCACCAATGAATA 43 + ILLUMINA 0.211021279 191 FALSE ACP1 +snp_rs10936922 snp_rs10936922 snp_rs10936922 Homo sapiens hg19 chr3 176675194 176675287 + GGGACTCTTCCAGATGCATTCTGAGTT 60 TAATTGTTGTTTTCCTAAGACGGAGTC 162 + ILLUMINA 0.104925708 235 FALSE ACP1 +snp_rs10184938 snp_rs10184938 snp_rs10184938 Homo sapiens hg19 chr2 9912919 9912986 + CTGTTCCCACAAGACTCGGGTGGTT 20 TCCATCTTTCAAAGACAGGCCTTAGAG 71 + ILLUMINA 0.553442177 209 FALSE ACP1 +snp_rs1028850 snp_rs1028850 snp_rs1028850 Homo sapiens hg19 chr13 40941401 40941454 + GGAATCTTAATCAGAACCTCAAAGCAC 53 GAGAATGGAAACAACCCACTCTATCCT 38 + ILLUMINA 0.842123958 195 FALSE ACP1 +snp_rs10913469 snp_rs10913469 snp_rs10913469 Homo sapiens hg19 chr1 177913436 177913498 + GAAAGGGAGAGCTGTCTGGAGAGAT 68 AAGAAATCCTACACCCTCCCACGCTTA 36 + ILLUMINA 0.683245768 204 FALSE ACP1 +snp_rs10490198 snp_rs10490198 snp_rs10490198 Homo sapiens hg19 chr2 67121590 67121670 + CCTGTCCTCCTCAAGTTAAGACAACCA 56 ATTGCTGCTCATGGTTACATGGTGAAC 62 + ILLUMINA 0.522152761 222 FALSE ACP1 +snp_rs1147960 snp_rs1147960 snp_rs1147960 Homo sapiens hg19 chr10 44971382 44971462 + CTGTGTCTAACATAGTTGTAACATGTC 31 ATGAATGGACAGAGCCATGTGACCA 87 + ILLUMINA 0.340999248 222 FALSE ACP1 +snp_rs10489168 snp_rs10489168 snp_rs10489168 Homo sapiens hg19 chr1 44727899 44727972 + GAAGTGTGACAAGGACAATAACCCCCA 39 ACTCCCTCTCTGGAAATCCAGCAGTT 76 + ILLUMINA 0.575405881 215 FALSE ACP1 +snp_rs11241298 snp_rs11241298 snp_rs11241298 Homo sapiens hg19 chr5 114282959 114283018 + TGCATCCACAACACATGAATTGAGGAC 61 AAAGAGAAGGGATGGGGATCGAGAAA 59 + ILLUMINA 0.818091155 201 FALSE ACP1 +snp_rs10935172 snp_rs10935172 snp_rs10935172 Homo sapiens hg19 chr3 135275607 135275671 + CTCCCACAGAAGCAGCATGCAGTCA 72 AGACTCACAGACAAGACTGTGAAGCT 60 + ILLUMINA 0.596164301 206 FALSE ACP1 +snp_rs10746385 snp_rs10746385 snp_rs10746385 Homo sapiens hg19 chr1 219706324 219706397 + GACAGAATCAGACCTATAAGGTTTCTC 48 TACAGTATGCCATCAAGCCCCCTTCAT 34 + ILLUMINA 0.567502432 215 FALSE ACP1 +snp_rs10834253 snp_rs10834253 snp_rs10834253 Homo sapiens hg19 chr11 24001879 24001968 + GCTCAATGCACTGATTTAAGTCATAAG 52 AGGAAAGTAGCAAATTATCCTCACACA 79 + ILLUMINA 0.391011516 231 FALSE ACP1 +snp_rs10068395 snp_rs10068395 snp_rs10068395 Homo sapiens hg19 chr5 178252283 178252356 + CGTCTAGTGGCTCACATGAATATTTCTG 60 TCCTCTCGGGTTCCTCCCCAGATATTA 63 + ILLUMINA 0.625549047 215 FALSE ACP1 +snp_rs10482536 snp_rs10482536 snp_rs10482536 Homo sapiens hg19 chrX 123884103 123884173 + AACAGTAGACCAAGATGGGGAGAGGTA 53 CCAAATGAAATAAGTGACCTACAAAGT 95 + ILLUMINA 0.453117563 212 FALSE ACP1 +snp_rs10512096 snp_rs10512096 snp_rs10512096 Homo sapiens hg19 chr9 82730243 82730336 + CCGATAAGAACTTTTGTGCCTCCTTC 40 ACATCATATTAGGTTCTGATTACAGATGC 72 + ILLUMINA 0.292524473 235 FALSE ACP1 +snp_rs10765017 snp_rs10765017 snp_rs10765017 Homo sapiens hg19 chr10 129168799 129168867 + TCTGGCAAGTGCAGGCTGATTTTATAC 52 TATGGTTAGCTGTGGCAGTGAGTGGTA 61 + ILLUMINA 0.795159865 210 FALSE ACP1 +snp_rs1049564 snp_rs1049564 snp_rs1049564 Homo sapiens hg19 chr14 20940526 20940576 + TTTCTCCCCCAGATACACCTATGAAGA 51 CTTTCCCCGAAGTACAGGTACTGGCAA 35 + ILLUMINA 0.881619662 192 FALSE ACP1 +snp_rs11094448 snp_rs11094448 snp_rs11094448 Homo sapiens hg19 chrX 147217312 147217367 + TGTGCCATGTCCTCTTAACATATAGCT 58 TCCAACCTTCTCTATGCAGTACATAGC 48 + ILLUMINA 0.854080172 197 FALSE ACP1 +snp_rs10852042 snp_rs10852042 snp_rs10852042 Homo sapiens hg19 chr15 96563051 96563103 + ACTCAACTACATAAACACCTTGTTCCC 42 CTACACCAAGTAAAATGGGTACATTTC 124 + ILLUMINA 0.457792624 194 FALSE ACP1 +snp_rs10492367 snp_rs10492367 snp_rs10492367 Homo sapiens hg19 chr12 28014882 28014943 + TCATCTTTTCGGCTCTTCTTGTCTCTG 38 GAACATGGTTTCATCAGTTTGAGCTAC 80 + ILLUMINA 0.738003928 203 FALSE ACP1 +snp_rs10519420 snp_rs10519420 snp_rs10519420 Homo sapiens hg19 chr4 138313081 138313150 + CATCATGTGAACCACTGCCTGTCGTTT 51 AGGAAAGAGTTAGACAAGGTGAATGCA 69 + ILLUMINA 0.73924162 211 FALSE ACP1 +snp_rs10278557 snp_rs10278557 snp_rs10278557 Homo sapiens hg19 chr7 15698951 15699007 + TTATTTTAAAATATGAAAGGTGTGGAAACC 819 TCAAAGTATCTGTAATGTCTAAACCCAG 94 + ILLUMINA 6.32E-27 198 FALSE ACP1 +snp_rs11017144 snp_rs11017144 snp_rs11017144 Homo sapiens hg19 chr10 132012880 132012933 + AAGGTCTGGGCATGGGAGGGCCCATTTT 73 ACTAGGATGTATTTCAGCATGTCTCGC 66 + ILLUMINA 0.664913089 195 FALSE ACP1 +snp_rs12651141 snp_rs12651141 snp_rs12651141 Homo sapiens hg19 chr4 89287627 89287677 + AACTAAGCATATTAGGGAGTGTGTTCT 39 TGTTCTTCTACTTGCCTCTGGAGGAT 67 + ILLUMINA 0.761725294 192 FALSE ACP1 +snp_rs1040247 snp_rs1040247 snp_rs1040247 Homo sapiens hg19 chr8 139533282 139533337 + GGCGGGGATTTGGGTCATTTATTGTT 48 CCTTAGCATGACAACCAAAGCAGCTA 59 + ILLUMINA 0.831417646 197 FALSE ACP1 +snp_rs10103493 snp_rs10103493 snp_rs10103493 Homo sapiens hg19 chr8 97352457 97352513 + CCACGCCTGCCGGAGCATCTATGACAA 14 TCACCCTTTGTGTCTTCCTGCCGCTTT 59 + ILLUMINA 0.578108916 198 FALSE ACP1 +snp_rs10180924 snp_rs10180924 snp_rs10180924 Homo sapiens hg19 chr2 86021832 86021893 + CAGCTCAGTGTTGGTGCCATCTGTCA 56 TTCCCTGTCAGCACCTCCCACGGAGA 53 + ILLUMINA 0.552464345 203 FALSE ACP1 +snp_rs10061008 snp_rs10061008 snp_rs10061008 Homo sapiens hg19 chr5 141744430 141744481 + TGCACGTTTCACAGTGAATGAAGGAAC 59 TCCTCAGCCTTCCTTCCTCGATGCTT 73 + ILLUMINA 0.79197988 193 FALSE ACP1 +snp_rs12570664 snp_rs12570664 snp_rs12570664 Homo sapiens hg19 chr10 1816215 1816270 + GCAAGAATTGAGTTGCTGCAGACTCA 108 ACTACTCCTGGCACTTAAATCTCAGAC 68 + ILLUMINA 0.617083905 197 FALSE ACP1 +snp_rs11017185 snp_rs11017185 snp_rs11017185 Homo sapiens hg19 chr10 132096075 132096165 + TCCTCTAATGCCGCTGGGTTAGG 184 AAAACCACAAACAGGAATCTCCTTGGG 63 + ILLUMINA 0.041126589 232 FALSE ACP1 +snp_rs10252308 snp_rs10252308 snp_rs10252308 Homo sapiens hg19 chr7 148501622 148501670 + GAGGTTGGAAACAGTATCACAGCAAC 57 TGCTGTGACCTAAGGGAACAAGGGAA 83 + ILLUMINA 0.806848985 190 FALSE ACP1 +snp_rs10490542 snp_rs10490542 snp_rs10490542 Homo sapiens hg19 chr2 207587227 207587313 + AGTCTGGGGTATGAGAACGAACTAA 34 CAGCTTTGAAAAGTTAGTATGACATCC 93 + ILLUMINA 0.331894043 228 FALSE ACP1 +snp_rs10776798 snp_rs10776798 snp_rs10776798 Homo sapiens hg19 chr1 115862165 115862222 + TACTGCAAAACCCTCGCCTCTGGGAT 25 AGTATGAACTCTGACCCCTACTCACCT 53 + ILLUMINA 0.719405389 199 FALSE ACP1 +snp_rs10894631 snp_rs10894631 snp_rs10894631 Homo sapiens hg19 chr11 132829598 132829646 + CATCCTAGTGGTTCACAGCGTTTCCAT 25 CCTGCTAACATAGCAGCCTGAGGA 55 + ILLUMINA 0.644587764 190 FALSE ACP1 +snp_rs10505173 snp_rs10505173 snp_rs10505173 Homo sapiens hg19 chr8 113486133 113486202 + TTCAGATTAGGAGCCATCCTTCTTGC 82 TTTTGCAGGAAGGACAGAGTACAATTT 101 + ILLUMINA 0.449201677 211 FALSE ACP1 +snp_rs10016530 snp_rs10016530 snp_rs10016530 Homo sapiens hg19 chr4 183824878 183824969 + TCTGAGGGAAGCCTCCACACCCA 54 CCTCAGCCTCCGGACCTAAGAAATAGA 103 + ILLUMINA 0.166741199 233 FALSE ACP1 +snp_rs11125183 snp_rs11125183 snp_rs11125183 Homo sapiens hg19 chr2 49013567 49013628 + CTCCTTTGAAGTAGCTTATCATGAGTC 47 ATCAAACCTCTTAGTGATGGCATACCC 37 + ILLUMINA 0.799737951 203 FALSE ACP1 +snp_rs10113311 snp_rs10113311 snp_rs10113311 Homo sapiens hg19 chr8 61888372 61888437 + CCCCTCTTCCTGCATTGTCTTCTT 135 CAGGAGCCAAGAGCTAAGTGAAGAGTA 80 + ILLUMINA 0.238729124 207 FALSE ACP1 +snp_rs10516939 snp_rs10516939 snp_rs10516939 Homo sapiens hg19 chr4 94574620 94574670 + CTCTTGAACTCTGAAACCCGAGAATGC 46 TCTCCAGCCTTGACGTCCCTGAAGAA 98 + ILLUMINA 0.674947194 192 FALSE ACP1 +snp_rs10790866 snp_rs10790866 snp_rs10790866 Homo sapiens hg19 chr11 127063152 127063229 + GAAGCTGCTTCCCAGAGTAAAAATGTG 68 AAGGGGGAGAGGCGTGTCACCTCCTTAT 44 + ILLUMINA 0.549780598 219 FALSE ACP1 +snp_rs1029864 snp_rs1029864 snp_rs1029864 Homo sapiens hg19 chr2 107784306 107784374 + TGTTATTGTATGGATCTGTTTCTTTTACC 141 TTATCTCAATCTAAACTGAGCAGACGG 36 + ILLUMINA 0.221138512 210 FALSE ACP1 +snp_rs10869715 snp_rs10869715 snp_rs10869715 Homo sapiens hg19 chr9 78780394 78780456 + AGAATGCTGTGGCCTTGATACATTCAC 45 ATAGGGCTGTGGGGCACCATTTCAATA 50 + ILLUMINA 0.854109314 204 FALSE ACP1 +snp_rs10248924 snp_rs10248924 snp_rs10248924 Homo sapiens hg19 chr7 138831626 138831699 + ATGTTACCAGGTAATAGTAAAGAGAGTAG 51 GAAGACAAAGAACCTAAGGGAAATAGG 105 + ILLUMINA 0.334366493 215 FALSE ACP1 +snp_rs10836419 snp_rs10836419 snp_rs10836419 Homo sapiens hg19 chr11 35580595 35580696 + AGCTAGCCTCCTTAAGAAGAGTAAAAG 50 AATGAATTGGCAATCAGAATCAACACC 75 + ILLUMINA 0.295688457 243 FALSE ACP1 +snp_rs10484150 snp_rs10484150 snp_rs10484150 Homo sapiens hg19 chr14 83637845 83637921 + GTGTAGGGCATGTTGAGAAGAAAACAC 67 AAAGATGTAGGATATACTGGATCCCGG 31 + ILLUMINA 0.6384027 218 FALSE ACP1 +snp_rs12719046 snp_rs12719046 snp_rs12719046 Homo sapiens hg19 chr7 51334392 51334472 + AAAGTGAGAAACGGCTTTTCTGGCTG 52 ATTGAGATAACCCAATTCAGGGTTGGG 55 + ILLUMINA 0.579925547 222 FALSE ACP1 +snp_rs1152562 snp_rs1152562 snp_rs1152562 Homo sapiens hg19 chr14 56879046 56879117 + CACTCTGCCATTAGAGAGAAGCAACT 70 ACAAGAAGACGGGTGGGTACTGCTCA 27 + ILLUMINA 0.499059095 213 FALSE ACP1 +snp_rs12679346 snp_rs12679346 snp_rs12679346 Homo sapiens hg19 chr8 34068371 34068443 + AATCAGGTACAGAGAGTATTGCAGAGT 49 ATGGCAACTGTAAGATTGATATGTGCG 34 + ILLUMINA 0.66746334 214 FALSE ACP1 +snp_rs11095604 snp_rs11095604 snp_rs11095604 Homo sapiens hg19 chrX 13143811 13143869 + CCACTGGCACATCTTCCTTGTTTTCA 65 GTCAAGAAGGAACACCCCATTATTCTC 53 + ILLUMINA 0.813724664 200 FALSE ACP1 +snp_rs10059981 snp_rs10059981 snp_rs10059981 Homo sapiens hg19 chr5 3619439 3619487 + CCATCACTGCACATGACAGGTGCTCA 70 TGTTGTCTCTCTAGCTTGGAGGACCAA 62 + ILLUMINA 0.782154177 190 FALSE ACP1 +snp_rs11070073 snp_rs11070073 snp_rs11070073 Homo sapiens hg19 chr13 94692842 94692897 + AATGCCTTCTGCTTAGCCCATTAAAGG 42 TGAAAGGCTGAGCCTATAGGCTGCATT 31 + ILLUMINA 0.843852663 197 FALSE ACP1 +snp_rs1144171 snp_rs1144171 snp_rs1144171 Homo sapiens hg19 chr6 91698172 91698250 + CAGGCCATATGCTGCCAAAGGAAACAA 51 TCTTTTCAGGCTATCCCATTTTCTGGC 82 + ILLUMINA 0.616778652 220 FALSE ACP1 +snp_rs1049269 snp_rs1049269 snp_rs1049269 Homo sapiens hg19 chr10 73819921 73819985 + GTCACAAATCAAGGAGCTGAGGAAGGA 68 AAACAGGCAAGGCTGGACCCCTGCAAT 60 + ILLUMINA 0.63914031 206 FALSE ACP1 +snp_rs10263803 snp_rs10263803 snp_rs10263803 Homo sapiens hg19 chr7 20437741 20437792 + ACATTAAAGGTAGCTGGATCCTTTGGA 54 TTAAGGATTGCAGCAAGCTTGACTGAC 43 + ILLUMINA 0.862933678 193 FALSE ACP1 +snp_rs11121704 snp_rs11121704 snp_rs11121704 Homo sapiens hg19 chr1 11293865 11293936 + TCTCAGTGATTGTTCATCCAGATTAAC 48 AACTCTTACCTCTTGTAAGGACAGCAC 76 + ILLUMINA 0.627370892 213 FALSE ACP1 +snp_rs10471977 snp_rs10471977 snp_rs10471977 Homo sapiens hg19 chr5 55750304 55750352 + CAGCGTTCAGTTCTCCTTAATTACAGG 50 AAGTCTTGACACCGCTCGGCAAGATCT 12 + ILLUMINA 0.767369442 190 FALSE ACP1 +snp_rs1005790 snp_rs1005790 snp_rs1005790 Homo sapiens hg19 chr5 160174868 160174920 + CACAGCGCTGTCATAGCTGTCTTTCAT 33 ATGAAGAGGTATCTGGGTCCAGCTGA 52 + ILLUMINA 0.829704017 194 FALSE ACP1 +snp_rs10863725 snp_rs10863725 snp_rs10863725 Homo sapiens hg19 chr1 208950718 208950838 + TCAGACTTCTTGCCACCAGAACTGT 162 GGAAGAGAAAGAGTCCATATAACATTGG 93 + ILLUMINA 0.033824951 262 FALSE ACP1 +snp_rs10930259 snp_rs10930259 snp_rs10930259 Homo sapiens hg19 chr2 167842556 167842611 + ACTGATGGAACTAGGAAGCTATAACCC 34 AAACTGATGAGGTTCTTTTGTGGCAC 76 + ILLUMINA 0.789566247 197 FALSE ACP1 +snp_rs10813743 snp_rs10813743 snp_rs10813743 Homo sapiens hg19 chr9 32109969 32110042 + TTTGCTCTGTCCAAGGGCCACAGCATTTT 72 AGAGATGAGCATGACTTGTGAGGTTAG 44 + ILLUMINA 0.54080386 215 FALSE ACP1 +snp_rs10906498 snp_rs10906498 snp_rs10906498 Homo sapiens hg19 chr10 13859315 13859378 + AGGAGAGGAGCTCTCAGTCAGTGCTTT 68 TCAAAACAGCACTTAACGTGTTGCAGG 33 + ILLUMINA 0.716514314 205 FALSE ACP1 +snp_rs10195834 snp_rs10195834 snp_rs10195834 Homo sapiens hg19 chr2 66826978 66827029 + ACCCTCTCCTTGCTCTTTTCCT 148 GGGAAAGCCTGTAAAGCTCTGAGGTTA 65 + ILLUMINA 0.159820735 193 FALSE ACP1 +snp_rs10248887 snp_rs10248887 snp_rs10248887 Homo sapiens hg19 chr7 23711688 23711734 + GAAGGTAAGTTTATAGGCACACTGGAG 32 TTCTCATGAAGAACTGCTGGGGCTAT 52 + ILLUMINA 0.859839636 188 FALSE ACP1 +snp_rs10135821 snp_rs10135821 snp_rs10135821 Homo sapiens hg19 chr14 97199808 97199866 + GTTTCTAGACTTGCCTCTTCATCCAGC 63 TTTGCTCACATTTCAGAGCTTCCGTTC 60 + ILLUMINA 0.839261548 200 FALSE ACP1 +snp_rs10999042 snp_rs10999042 snp_rs10999042 Homo sapiens hg19 chr10 71707334 71707381 + AGCCTGGGGCCTGATCCTCACATGGAA 63 AGATCCATTGCTACCTTGTCCTTGC 38 + ILLUMINA 0.642754309 189 FALSE ACP1 +snp_rs10036347 snp_rs10036347 snp_rs10036347 Homo sapiens hg19 chr5 56694562 56694640 + TAACGTGGCATTGTCATTCAACTTATT 40 ATTAAAAAGCAGTTGGTGATGTGAGAC 84 + ILLUMINA 0.4353583 220 FALSE ACP1 +snp_rs10189159 snp_rs10189159 snp_rs10189159 Homo sapiens hg19 chr2 50714476 50714545 + CAGGTCTTTCTGACGTCAAAGACTGT 88 TAAGGAGCACTGGAAGTACCCTCTAGT 31 + ILLUMINA 0.608621013 211 FALSE ACP1 +snp_rs10491907 snp_rs10491907 snp_rs10491907 Homo sapiens hg19 chr9 9963859 9963931 + TGAAGGGTACCATGCACTAACTCAATG 23 GCATTAATATATATGAATGGCACATCAGAG 198 + ILLUMINA 0.049106968 214 FALSE ACP1 +snp_rs10737814 snp_rs10737814 snp_rs10737814 Homo sapiens hg19 chr1 237469221 237469276 + TTCTTCAACCTGGTTGATGGACTCATG 49 AATGTTGGCAATACATGAAAAATTATGTC 285 + ILLUMINA 0.002100647 197 FALSE ACP1 +snp_rs10503087 snp_rs10503087 snp_rs10503087 Homo sapiens hg19 chr18 61476361 61476445 + AGTGATCCGAATGGAAAGGGAAGTGT 21 TGTGATGAGTGAGGGCAGATGAGCTAT 72 + ILLUMINA 0.484485528 226 FALSE ACP1 +snp_rs10094564 snp_rs10094564 snp_rs10094564 Homo sapiens hg19 chr8 673456 673552 + TCCACTTAATAGACTTACAAACAGAAAAG 120 TGCTCTCTCAGTGAACAGCAGCTCTA 84 + ILLUMINA 0.160482166 238 FALSE ACP1 +snp_rs11662907 snp_rs11662907 snp_rs11662907 Homo sapiens hg19 chr18 21455480 21455528 + AGGAAACAAGACCAACCCAAGGAGA 68 CTGATTGTGGCATGATTGTCTAAATCTC 69 + ILLUMINA 0.697121256 190 FALSE ACP1 +snp_rs10093381 snp_rs10093381 snp_rs10093381 Homo sapiens hg19 chr8 87628292 87628377 + CAGGGACAGATAGCAGCAGTGAAGGAA 60 CTTTTTATTAACATACTTGGATAGCACATG 95 + ILLUMINA 0.190601841 227 FALSE ACP1 +snp_rs10741808 snp_rs10741808 snp_rs10741808 Homo sapiens hg19 chr11 20020803 20020858 + TGCCTGGCATAAATCAACCCTGCTGTT 41 TGCTTTGGGAAAATGTGGGGTTT 113 + ILLUMINA 0.354015863 197 FALSE ACP1 +snp_rs11563212 snp_rs11563212 snp_rs11563212 Homo sapiens hg19 chr2 234869276 234869363 + CCATTCTCCTGTTTAGAGGTTTGAACTG 59 CTTTCTCCTTAGTCTGCTGACCTTCA 41 + ILLUMINA 0.34051809 229 FALSE ACP1 +snp_rs10514496 snp_rs10514496 snp_rs10514496 Homo sapiens hg19 chr16 80456324 80456376 + GTTTGAGAAATGCGATTTTCTGAGTCC 43 TCATGTTTCTGGTGGCATGCTCGGTT 25 + ILLUMINA 0.816692977 194 FALSE ACP1 +snp_rs11633318 snp_rs11633318 snp_rs11633318 Homo sapiens hg19 chr15 77602616 77602693 + GTTTAAACTTATGGCCAAATCTGGATG 40 TTCTCTGCAGGTTTCATATCAAAGCAC 82 + ILLUMINA 0.441984635 219 FALSE ACP1 +snp_rs10509550 snp_rs10509550 snp_rs10509550 Homo sapiens hg19 chr10 90219207 90219273 + CAAGACCAAATCCACTACTTTTATTGG 54 ATTTTAGAGTCAACAGAGCCCCAGGA 89 + ILLUMINA 0.596984845 208 FALSE ACP1 +snp_rs10758 snp_rs10758 snp_rs10758 Homo sapiens hg19 chr2 113409907 113409988 + GGCGTACGCATAGTCTGCATGTTGTAT 9 TATCAGTCACTGGTACAGTTAGTCTTG 50 + ILLUMINA 0.43987156 223 FALSE ACP1 +snp_rs10281519 snp_rs10281519 snp_rs10281519 Homo sapiens hg19 chr7 90909948 90909993 + CCTTCCCAGGGAATTCACTAATCA 53 CTGGGAAATGTGAGTAAGACAGGACT 81 + ILLUMINA 0.642655414 187 FALSE ACP1 +snp_rs10860784 snp_rs10860784 snp_rs10860784 Homo sapiens hg19 chr12 102172954 102173002 + AACTGCTCTCTAGTCACCTCTAATCAC 39 AACTAGAGCCTCACAAATTCTGAGACA 76 + ILLUMINA 0.833925354 190 FALSE ACP1 +snp_rs11077405 snp_rs11077405 snp_rs11077405 Homo sapiens hg19 chr17 76969792 76969858 + ATTTTAGAACTCCGGGGGTCCTCGA 22 TGAAGTAACTGTGACCTTTCAACCAGG 55 + ILLUMINA 0.631855495 208 FALSE ACP1 +snp_rs10449246 snp_rs10449246 snp_rs10449246 Homo sapiens hg19 chr1 224936216 224936267 + GGAGCGCTAATGCATAATTTTGTGAGG 32 ATGGCTGTATCTGAGAATATTGGATGA 87 + ILLUMINA 0.708845715 193 FALSE ACP1 +snp_rs10185855 snp_rs10185855 snp_rs10185855 Homo sapiens hg19 chr2 101642181 101642232 + AAGTCTTACGCAGAACATGAAAGGAAG 40 GCTTACGCACCAAGTCTGTATTTATAC 84 + ILLUMINA 0.736144802 193 FALSE ACP1 +snp_rs10184153 snp_rs10184153 snp_rs10184153 Homo sapiens hg19 chr2 182220086 182220159 + GTTTTCTGAGACCAGATTATTTTCCTGG 108 GTCAAAAACTAATCGTGTATATGTCTGC 35 + ILLUMINA 0.402172069 215 FALSE ACP1 +snp_rs10771328 snp_rs10771328 snp_rs10771328 Homo sapiens hg19 chr12 27425285 27425341 + AGAATTAGCACAGCGTTGGAATGACC 28 AGGAAGGACTGGGAAAGTAGCTCTTT 80 + ILLUMINA 0.724169864 198 FALSE ACP1 +snp_rs11563675 snp_rs11563675 snp_rs11563675 Homo sapiens hg19 chr7 126873844 126873897 + CCAGAGGGAGCCTTGAAGCGTCTTAGA 43 CAGCCTGGTGTTCCTTATGTATTCAAG 96 + ILLUMINA 0.670020123 195 FALSE ACP1 +snp_rs10148795 snp_rs10148795 snp_rs10148795 Homo sapiens hg19 chr14 33845222 33845303 + GCATCACTCTGACCCTGGCATTTATT 59 ACCGTTATTTCCCTATATTGTACTGCC 54 + ILLUMINA 0.564029693 223 FALSE ACP1 +snp_rs10516506 snp_rs10516506 snp_rs10516506 Homo sapiens hg19 chr4 104595153 104595243 + CCAAATGTGTACAACTCCATTCAATTTC 121 GAGGCAGAACACTTGGAAGCTTTAGT 61 + ILLUMINA 0.251340571 232 FALSE ACP1 +snp_rs10178199 snp_rs10178199 snp_rs10178199 Homo sapiens hg19 chr2 127756865 127756948 + GGGAGCCCCTCCTGGAAAATATGAAA 52 GTTGGCAGGCAACCTGGGATCCAGGTA 52 + ILLUMINA 0.440003964 225 FALSE ACP1 +snp_rs10516603 snp_rs10516603 snp_rs10516603 Homo sapiens hg19 chr4 115467380 115467430 + TTTTGTCACTAGTCTTCTTCGGATAAG 51 ATACTTTGACACCGCCCTTTCATTTTT 69 + ILLUMINA 0.702227708 192 FALSE ACP1 +snp_rs10088698 snp_rs10088698 snp_rs10088698 Homo sapiens hg19 chr8 48654691 48654751 + ACGCACCCCTCATGCTGTTAAAGCTT 52 TACCTGCTCACATTCTCCTCAACAGA 97 + ILLUMINA 0.589067948 202 FALSE ACP1 +snp_rs10103826 snp_rs10103826 snp_rs10103826 Homo sapiens hg19 chr8 135495979 135496032 + AGCAGCATAGATAGCTCGATAGAAACC 40 TCCCCTTGAGACCCCATGTCTTCCTT 64 + ILLUMINA 0.817672011 195 FALSE ACP1 +snp_rs1042606 snp_rs1042606 snp_rs1042606 Homo sapiens hg19 chr10 112270593 112270642 + AAAGAAGTTGCTGGACCAGGAGAAAAG 62 TTTGTAGGGACATGATCAGCATCCTG 46 + ILLUMINA 0.870011729 191 FALSE ACP1 +snp_rs10497276 snp_rs10497276 snp_rs10497276 Homo sapiens hg19 chr2 166856914 166856971 + TCAAAACATTTAGAAATAACCCCCTATTC 278 GAATTTTGAGTCCTGTGGGCCTAAAAG 47 + ILLUMINA 0.003394502 199 FALSE ACP1 +snp_rs10753764 snp_rs10753764 snp_rs10753764 Homo sapiens hg19 chr1 167760634 167760737 + CCTACACTGAGAACAATCCTGTGCCAA 45 TGTTTGAAAGATTATATGGCTTACCCA 98 + ILLUMINA 0.204817817 245 FALSE ACP1 +snp_rs1002745 snp_rs1002745 snp_rs1002745 Homo sapiens hg19 chr10 82656204 82656270 + TCCAGCAAAGCCCCACGGCATTATAAA 32 CAGGGAAATTGGAGCAGAAGCTTGGT 79 + ILLUMINA 0.613980515 208 FALSE ACP1 +snp_rs10073948 snp_rs10073948 snp_rs10073948 Homo sapiens hg19 chr5 82134537 82134591 + CTGCAATACCTCAACTGAGAAGGGCTTA 39 TGACAACAAAGGACAGGGGGTGTTGAA 53 + ILLUMINA 0.854008791 196 FALSE ACP1 +snp_rs10830004 snp_rs10830004 snp_rs10830004 Homo sapiens hg19 chr10 133212128 133212221 + GACCTTGTGCTGTGCATGTTTTCCTT 66 CTAAATACACTTCAGAAGAGATGGGCA 109 + ILLUMINA 0.296586818 235 FALSE ACP1 +snp_rs10128762 snp_rs10128762 snp_rs10128762 Homo sapiens hg19 chr12 74681809 74681869 + TCCACAGGAGGTATTGAAGCTCGTTA 37 AAATCAAGGCACATCTCTAGTTATTTTC 125 + ILLUMINA 0.347800351 202 FALSE ACP1 +snp_rs10109209 snp_rs10109209 snp_rs10109209 Homo sapiens hg19 chr8 5528860 5528911 + AGCGTGGTAATGTGTGGCACAGGTGAT 25 TGTCCTAGAGCAATGAAAGACGCTGT 32 + ILLUMINA 0.771242335 193 FALSE ACP1 +snp_rs1026580 snp_rs1026580 snp_rs1026580 Homo sapiens hg19 chr10 13981069 13981144 + TAGAATTCCCAGAATAGCACCATCCTC 51 AATTGCCTGGGATTAATCAATGTAGGG 41 + ILLUMINA 0.722675516 217 FALSE ACP1 +snp_rs10505299 snp_rs10505299 snp_rs10505299 Homo sapiens hg19 chr8 118426643 118426707 + CCACTTTCATATTAACCCCCACAAAAT 42 CAAGCAATGTATTGCTCCCTCTGTTG 54 + ILLUMINA 0.647721082 206 FALSE ACP1 +snp_rs10919336 snp_rs10919336 snp_rs10919336 Homo sapiens hg19 chr1 170216721 170216792 + CTCCCCCTGAAGCAAATCCTAAACCAA 68 AAGTTAGAAGCATTTAATGAAATAAAGCAG 610 + ILLUMINA 8.64E-15 213 FALSE ACP1 +snp_rs10505532 snp_rs10505532 snp_rs10505532 Homo sapiens hg19 chr8 130021864 130021933 + GACTCCTGATACACAGAAATTTGAGTT 79 GTTCTAACAACACCTAATCTGTTTCTC 91 + ILLUMINA 0.46771952 211 FALSE ACP1 +snp_rs10518287 snp_rs10518287 snp_rs10518287 Homo sapiens hg19 chr19 35399305 35399389 + GATGTGCTCCACCATGTAACGACATA 42 AAAAGTCCCTGTATTCCTGTCTCCCA 91 + ILLUMINA 0.44819409 226 FALSE ACP1 +snp_rs10955157 snp_rs10955157 snp_rs10955157 Homo sapiens hg19 chr8 99227053 99227147 + TCTAATATGGAAGATGAACTCATCCCT 80 GTTAACAGAAATATCCCTCTGGGCCCA 69 + ILLUMINA 0.358330774 236 FALSE ACP1 +snp_rs10487324 snp_rs10487324 snp_rs10487324 Homo sapiens hg19 chr7 110036520 110036568 + GATTAGGGGCCATGTTTCCTGGAATAG 41 ACTGTTCTGGGTCATTTAGGTCAGAC 54 + ILLUMINA 0.910875574 190 FALSE ACP1 +snp_rs10519096 snp_rs10519096 snp_rs10519096 Homo sapiens hg19 chr15 61289830 61289923 + GCTGCTTCTCAAATAGTGTGTTTTAAA 100 TTTTCTCCCATCTGGACCTTGAAGT 61 + ILLUMINA 0.211654611 235 FALSE ACP1 +snp_rs10968281 snp_rs10968281 snp_rs10968281 Homo sapiens hg19 chr9 28013206 28013269 + CACTGGGTCTCTAGTAACAATCAGGAT 54 GAAGGGTCTTATGATCCAGACGATTGT 23 + ILLUMINA 0.755247179 205 FALSE ACP1 +snp_rs11060670 snp_rs11060670 snp_rs11060670 Homo sapiens hg19 chr12 130515637 130515690 + TCTCCCATCTTGTGCCCCTCCTCAGAT 77 CATCACCGGGAGTCCTGAGAGCTCAT 37 + ILLUMINA 0.645938591 195 FALSE ACP1 +snp_rs10859402 snp_rs10859402 snp_rs10859402 Homo sapiens hg19 chr12 93409765 93409825 + TGAGGTTGTTCATGCAAAGGGATCCA 45 TGCAGGGAGGGAATTTTCATGCAATC 68 + ILLUMINA 0.749309572 202 FALSE ACP1 +snp_rs1108958 snp_rs1108958 snp_rs1108958 Homo sapiens hg19 chr13 51822103 51822156 + ATGTTCAACCAAACCGAAAGAAGCCAG 35 TGATCTGAAAGTAACTGGCCCATCCT 38 + ILLUMINA 0.827366875 195 FALSE ACP1 +snp_rs10869756 snp_rs10869756 snp_rs10869756 Homo sapiens hg19 chr9 78959243 78959314 + GTAAACCAATCCAGGCAGAGCTGCTCA 82 AAGAATTAGCCTTCCAAACAAACTGCA 101 + ILLUMINA 0.430023894 213 FALSE ACP1 +snp_rs10502370 snp_rs10502370 snp_rs10502370 Homo sapiens hg19 chr18 8454421 8454471 + GATCACATCTCTCTGGACATACCCTCA 47 ACTCTGTGATTGACAAATCTTTCACCT 71 + ILLUMINA 0.784698937 192 FALSE ACP1 +snp_rs10000030 snp_rs10000030 snp_rs10000030 Homo sapiens hg19 chr4 103374075 103374128 + TGATGTCTTCCTTCTTTTTAGGCAAAA 218 ACCAATATCTATGAATCTGTATAGCTTGG 112 + ILLUMINA 0.022909171 195 FALSE ACP1 +snp_rs10746432 snp_rs10746432 snp_rs10746432 Homo sapiens hg19 chr1 210837610 210837664 + GCCTCATAGGCTTATTAAGATTAAAACTC 69 CTGAACATGGTTAAACTAAGTGCTGTC 50 + ILLUMINA 0.622318136 196 FALSE ACP1 +snp_rs10438441 snp_rs10438441 snp_rs10438441 Homo sapiens hg19 chr15 92862529 92862587 + AGCCTCTCAACTTCCCACCGAGCATGT 43 AGCTCTCCTCCCAGTATCCCCCATATA 63 + ILLUMINA 0.721013335 200 FALSE ACP1 +snp_rs1110240 snp_rs1110240 snp_rs1110240 Homo sapiens hg19 chr1 21324849 21324927 + AATACAAGGCATGTCAAGGCAAACAGC 46 TTCCTCAGCTAAATCATAGAGTACTTG 58 + ILLUMINA 0.513382127 220 FALSE ACP1 +snp_rs10110604 snp_rs10110604 snp_rs10110604 Homo sapiens hg19 chr8 16502996 16503053 + GCTGCACAGTTGTCTTAGTTTTCTCC 51 TTGGCAAGGGTCAATACACATTGGTTC 43 + ILLUMINA 0.843584667 199 FALSE ACP1 +snp_rs10502432 snp_rs10502432 snp_rs10502432 Homo sapiens hg19 chr18 19827394 19827445 + GTGCTCAGGGTTCTGGAGTTTTGACAA 48 TTTCTGTCAAGCTGGACATGATTCTGC 56 + ILLUMINA 0.917357342 193 FALSE ACP1 +snp_rs10874743 snp_rs10874743 snp_rs10874743 Homo sapiens hg19 chr1 91952023 91952090 + GAAACTGTGACAGGCAAACTTGTTAGC 74 CTTCAACCTGTGAAGTGTTCCTCTAGC 48 + ILLUMINA 0.701461162 209 FALSE ACP1 +snp_rs10090419 snp_rs10090419 snp_rs10090419 Homo sapiens hg19 chr8 124028550 124028599 + GCTAAGAGAACTTAAACCCAAGCCTAC 59 TCCGCTTAAACCCTTCTTGGCAGCAA 57 + ILLUMINA 0.876469624 191 FALSE ACP1 +snp_rs10496687 snp_rs10496687 snp_rs10496687 Homo sapiens hg19 chr2 133269176 133269237 + GTGTGAGTAGGGTTCACAAATCAAAAA 30 ACACTGACTTAATATGTACTACGTGCC 50 + ILLUMINA 0.710425199 203 FALSE ACP1 +snp_rs10790037 snp_rs10790037 snp_rs10790037 Homo sapiens hg19 chr11 114665080 114665137 + TCTCATTCTAGATGAAGCACCCTTCCC 54 TGTGAATGTGTACCTACCACACCAG 50 + ILLUMINA 0.760277944 199 FALSE ACP1 +snp_rs10895457 snp_rs10895457 snp_rs10895457 Homo sapiens hg19 chr11 103416570 103416625 + GAGGTCAATGCAATACAGAAGTGTAGC 70 GCTGGTTGTCATGACATTAATGCTACC 40 + ILLUMINA 0.838645904 197 FALSE ACP1 +snp_rs12604608 snp_rs12604608 snp_rs12604608 Homo sapiens hg19 chr18 42405998 42406053 + AAAGAGTGACTAGTACCTTGATGTTTC 39 GAGTTCAAAGGAAAGTTCTAGTGTAATG 98 + ILLUMINA 0.521149416 197 FALSE ACP1 +snp_rs11171681 snp_rs11171681 snp_rs11171681 Homo sapiens hg19 chr12 56193146 56193212 + TGTTCAAAGTTTAGGACTCAACGGCTC 35 CAAGAGAGAACAGAGTGCTACTTCAGA 72 + ILLUMINA 0.753497256 208 FALSE ACP1 +snp_rs10961505 snp_rs10961505 snp_rs10961505 Homo sapiens hg19 chr9 14410504 14410576 + AGGGCAGAGTAAACTACTATGCATAAGG 49 AACAAAGAGGTTGAAGGTTATGAGCAG 113 + ILLUMINA 0.472851967 214 FALSE ACP1 +snp_rs10497933 snp_rs10497933 snp_rs10497933 Homo sapiens hg19 chr2 212141596 212141648 + GCCTGCCTTCAAGTGTTTGAAAGCTT 72 CTTGAAGAGAAGACCATTGATCTGACA 44 + ILLUMINA 0.815850902 194 FALSE ACP1 +snp_rs12587583 snp_rs12587583 snp_rs12587583 Homo sapiens hg19 chr14 69510363 69510412 + GAAGAAAGTGACTTGGCCCATGCCT 51 AGAGCATGAGGGGAAGAGGTTTCTT 81 + ILLUMINA 0.655533052 191 FALSE ACP1 +snp_rs10966009 snp_rs10966009 snp_rs10966009 Homo sapiens hg19 chr9 23651348 23651413 + TGATGCACAGTCCTGAGTCCTACGAAT 37 GGGATGCAGTGGTGGCAAGAAGTAA 95 + ILLUMINA 0.531626857 207 FALSE ACP1 +snp_rs1160246 snp_rs1160246 snp_rs1160246 Homo sapiens hg19 chr9 119993006 119993061 + AGCAACCCATAGTAAGTGAACCAAAGAG 42 AGAGAAGGCTGTGGACTGAAAACAA 116 + ILLUMINA 0.496012169 197 FALSE ACP1 +snp_rs11096672 snp_rs11096672 snp_rs11096672 Homo sapiens hg19 chr2 20743635 20743702 + AGGGGATTGCTCCAAACTTTGCTAAC 37 CAGCGTTCCCTCTCACAGGAGCTATTA 55 + ILLUMINA 0.707692541 209 FALSE ACP1 +snp_rs10926264 snp_rs10926264 snp_rs10926264 Homo sapiens hg19 chr1 235779057 235779105 + ATGAACATCACATAGACATAGCCATTA 61 AAGGTCGTGGTGGGCTCACTCTCTGT 35 + ILLUMINA 0.585085977 190 FALSE ACP1 +snp_rs10050018 snp_rs10050018 snp_rs10050018 Homo sapiens hg19 chr4 183349539 183349586 + GTCAACAATTGTTCACTCAAGGAAGTG 39 AGGATCTGATCAATTTGATGAGTCTTT 81 + ILLUMINA 0.654680237 189 FALSE ACP1 +snp_rs10243669 snp_rs10243669 snp_rs10243669 Homo sapiens hg19 chr7 45915829 45915895 + CATCAGGGTGAGGCCATGTTGAATCT 49 CAGAAAAATCTGATGTGGCAGGTGCT 72 + ILLUMINA 0.639578438 208 FALSE ACP1 +snp_rs10767843 snp_rs10767843 snp_rs10767843 Homo sapiens hg19 chr11 30436295 30436376 + CCTCAATTCAGTTACTTTCGCTATTTT 66 TGTCCTCTCCAGCGACAGGCAAAAAT 76 + ILLUMINA 0.397654228 223 FALSE ACP1 +snp_rs1040173 snp_rs1040173 snp_rs1040173 Homo sapiens hg19 chr2 146120432 146120479 + GGACAAAGGGAGTATGGAACATTTGAG 38 AGGGGAATACAACATGATTTGGATGC 76 + ILLUMINA 0.799758636 189 FALSE ACP1 +snp_rs10490012 snp_rs10490012 snp_rs10490012 Homo sapiens hg19 chr2 234843415 234843500 + CAGCACTTCAAGAAGATCACTATCAGC 48 GTAAATGAAAATGTGACCTCCTGCCA 116 + ILLUMINA 0.217168479 227 FALSE ACP1 +snp_rs10500844 snp_rs10500844 snp_rs10500844 Homo sapiens hg19 chr11 19250076 19250155 + TCATGGAATAAATTCACTTAACCCCAC 84 AAAATAGCTTGTATTAAGAGCAGGGGC 75 + ILLUMINA 0.449062088 221 FALSE ACP1 +snp_rs10143478 snp_rs10143478 snp_rs10143478 Homo sapiens hg19 chr14 33442533 33442626 + GTGGGGTAGTATGGGGTTTTTGTCTCT 46 CAGAATTTTGTTAGTAAGTTTGGAATTGC 114 + ILLUMINA 0.185383354 235 FALSE ACP1 +snp_rs10493230 snp_rs10493230 snp_rs10493230 Homo sapiens hg19 chr1 58050024 58050109 + GTGAATCTGTTGTGATTCTGCAGGCT 58 AATCTTTGGTCCTAGACATAGTCCCTG 49 + ILLUMINA 0.374515269 227 FALSE ACP1 +snp_rs10489562 snp_rs10489562 snp_rs10489562 Homo sapiens hg19 chr1 96058458 96058528 + AAACCTAACTCTCTCAGTTCTGTGCTC 57 TGACGTGCAGTTCAGCAGCAGAATCT 83 + ILLUMINA 0.645112798 212 FALSE ACP1 +snp_rs109894 snp_rs109894 snp_rs109894 Homo sapiens hg19 chr5 79067989 79068064 + GAAACCAATGACAGTTCCATTTGTAGG 52 AATAGAACAATACAAGGGGTTCTTTGC 60 + ILLUMINA 0.572781688 217 FALSE ACP1 +snp_rs10914880 snp_rs10914880 snp_rs10914880 Homo sapiens hg19 chr1 34620692 34620739 + CCTGCCTGGATCCATGCATATTTGAA 57 GACTGAGGGTAGGATTAATTCAAATGT 88 + ILLUMINA 0.683500629 189 FALSE ACP1 +snp_rs11662069 snp_rs11662069 snp_rs11662069 Homo sapiens hg19 chr18 29829266 29829314 + GTATTTTTGTGTCCCCCTGAGTGG 55 AGCCAAGGTTAGAGAGAGATTTACACA 118 + ILLUMINA 0.422195942 190 FALSE ACP1 +snp_rs10996274 snp_rs10996274 snp_rs10996274 Homo sapiens hg19 chr10 66957067 66957133 + TCAAAACTGTGCATGTTGTGTAAGCC 73 GGAAATATATCCTCATCAGTCAGGACAG 72 + ILLUMINA 0.600973946 208 FALSE ACP1 +snp_rs10849968 snp_rs10849968 snp_rs10849968 Homo sapiens hg19 chr12 109694239 109694289 + CCAATTTGGGGAATGATTTCTGCAGTG 93 ACAGACACTGGCACTCTGAATTCCAT 58 + ILLUMINA 0.729389354 192 FALSE ACP1 +snp_rs10496397 snp_rs10496397 snp_rs10496397 Homo sapiens hg19 chr2 106184359 106184411 + ACATTTAGTTATAAGTCAGCTGCGTTT 39 AATGTTTTTAAAGCACTGCGTCCCCTC 53 + ILLUMINA 0.714652589 194 FALSE ACP1 +snp_rs10744116 snp_rs10744116 snp_rs10744116 Homo sapiens hg19 chr12 16476792 16476847 + GTTCCTCCTCTATCTTGTGAACTGG 74 GTGATCTTGGCAATAACTTGGAAGATT 70 + ILLUMINA 0.62372819 197 FALSE ACP1 +snp_rs10521575 snp_rs10521575 snp_rs10521575 Homo sapiens hg19 chrX 116625965 116626021 + ACAAGGCATCCAAATTATTTCATTGTG 160 CTAAGCGCAGTAAACCCAGGATGGAAT 46 + ILLUMINA 0.21337901 198 FALSE ACP1 +snp_rs11104117 snp_rs11104117 snp_rs11104117 Homo sapiens hg19 chr12 87224946 87225021 + TGGAAACCCATGAAGAGTATACCTTTT 50 CTGGGAGGAACAATACTATGTAGAGGG 34 + ILLUMINA 0.538917148 217 FALSE ACP1 +snp_rs1060912 snp_rs1060912 snp_rs1060912 Homo sapiens hg19 chr6 52389629 52389694 + TTTTTCTTCCATAGGGAGCGAGAATGG 79 TGAAAGTATTATGCCTACTTCCAACAG 76 + ILLUMINA 0.603099147 207 FALSE ACP1 +snp_rs10865643 snp_rs10865643 snp_rs10865643 Homo sapiens hg19 chr3 69099644 69099733 + GCAAATGAACAACCAAGATTATGTCTG 48 TAGTAATTCTAATTAACTGGGGCACAT 55 + ILLUMINA 0.375170888 231 FALSE ACP1 +snp_rs10153199 snp_rs10153199 snp_rs10153199 Homo sapiens hg19 chr16 860595 860640 + GGTGTGGGACAGGTCTGGGTGACTT 63 CTCGGATCTATGGAGGGTTTGCCTTT 42 + ILLUMINA 0.648977912 187 FALSE ACP1 +snp_rs1002897 snp_rs1002897 snp_rs1002897 Homo sapiens hg19 chr2 66464244 66464324 + GAGGGAGACTCCATCTCAAAAAGAAAA 1200 AGCCGCCAAATCTATATACAAACCAGG 61 + ILLUMINA 2.03E-58 222 FALSE ACP1 +snp_rs11113551 snp_rs11113551 snp_rs11113551 Homo sapiens hg19 chr12 108248223 108248301 + ACCTACTCTGCTCAGAATTGTGTTGTC 57 TTTTTCTGGGCTTGTACAAAACGTGT 48 + ILLUMINA 0.558065379 220 FALSE ACP1 +snp_rs1030356 snp_rs1030356 snp_rs1030356 Homo sapiens hg19 chr4 141826698 141826749 + GAAATGTATAAAGGGGAACTTGTTCGG 76 AAGGCACCTCCCAATCCCAGGCCTGT 106 + ILLUMINA 0.440930708 193 FALSE ACP1 +snp_rs11048057 snp_rs11048057 snp_rs11048057 Homo sapiens hg19 chr12 25623883 25623957 + GCCTAATACCCGGCTTAAGAAACAAAAC 39 GAAGAACATGAATCAGTTTGAGCTGAT 74 + ILLUMINA 0.58109513 216 FALSE ACP1 +snp_rs1156232 snp_rs1156232 snp_rs1156232 Homo sapiens hg19 chr4 126433134 126433190 + GGTGATTTCTCACAGGAGAAGTTACGT 53 AAAAAGGCAAGGCATGTTCTACCAT 46 + ILLUMINA 0.726193821 198 FALSE ACP1 +snp_rs11074037 snp_rs11074037 snp_rs11074037 Homo sapiens hg19 chr15 92604379 92604427 + AATGACGTGCCTTATACGTGTTCGGT 7 GGTGTTTAGAGGCTGACTGGCTCAT 73 + ILLUMINA 0.622865094 190 FALSE ACP1 +snp_rs10257276 snp_rs10257276 snp_rs10257276 Homo sapiens hg19 chr7 136370731 136370780 + TAAGAGCCTCACTCATTGATTTCACCC 53 AAATTATCTGGGTTACAGTCTCGGCTC 28 + ILLUMINA 0.86350649 191 FALSE ACP1 +snp_rs12588458 snp_rs12588458 snp_rs12588458 Homo sapiens hg19 chr14 67830774 67830841 + GGTTGGGTGGATCAAAGGGAATAATTG 50 AAAAGAATTATGAGAGGAGGATGCATT 84 + ILLUMINA 0.544372964 209 FALSE ACP1 +snp_rs10077711 snp_rs10077711 snp_rs10077711 Homo sapiens hg19 chr5 179587663 179587725 + AGGAAAATTGGCTCCGAATCTCAGTAG 31 AGCTTGAGAACGTCCCTGTAAAACCA 50 + ILLUMINA 0.813499927 204 FALSE ACP1 +snp_rs10279558 snp_rs10279558 snp_rs10279558 Homo sapiens hg19 chr7 114862850 114862916 + AGACAGAGAAAGAGCCTGGGCCAAAAA 219 TGGTAAGTCAAGTTAGTTTATCTGCAA 100 + ILLUMINA 0.025960892 208 FALSE ACP1 +snp_rs10508853 snp_rs10508853 snp_rs10508853 Homo sapiens hg19 chr10 37069301 37069370 + TTGCTAATAGCTGCCTTGAGTACTATG 45 AAAACTAAGGGACAGAATAGCTTCAGT 67 + ILLUMINA 0.56321583 211 FALSE ACP1 +snp_rs10793421 snp_rs10793421 snp_rs10793421 Homo sapiens hg19 chr7 54704926 54704977 + ACCCAGCTCAGGTGAACAGTTTTTCA 58 GTCTATTACCTTTTTGAGGGGGTGACA 65 + ILLUMINA 0.880437355 193 FALSE ACP1 +snp_rs10432009 snp_rs10432009 snp_rs10432009 Homo sapiens hg19 chr17 13091362 13091427 + GAGCTTCTAAGCATACTTTCAAAGGCA 43 ATTTCTAAGCCACAGACTAAAAGATTATG 149 + ILLUMINA 0.198212105 207 FALSE ACP1 +snp_rs11002643 snp_rs11002643 snp_rs11002643 Homo sapiens hg19 chr10 80478423 80478469 + TCTTTTGTTGTATGTGTAGACATGGG 126 TGTCAAGGAGCCAGCCAGGAGGAGT 135 + ILLUMINA 0.164523918 188 FALSE ACP1 +snp_rs10519010 snp_rs10519010 snp_rs10519010 Homo sapiens hg19 chr15 60551836 60551899 + CTAATCTGCACAAGTCTAGAAAAAGAGG 50 AACCTTCGAACCTGTGACATAATCTCC 43 + ILLUMINA 0.786450461 205 FALSE ACP1 +snp_rs11576172 snp_rs11576172 snp_rs11576172 Homo sapiens hg19 chr1 217324574 217324632 + TGGGTAGGTAATAGAGCCAAGTATATAG 43 AAGTTTCTGAAGCACCATATCCTGGAC 58 + ILLUMINA 0.765165215 200 FALSE ACP1 +snp_rs11133601 snp_rs11133601 snp_rs11133601 Homo sapiens hg19 chr5 10104487 10104579 + GTTCTTATAGCTTACCATTTTTACCACC 92 GATTTAAAGTGTCTCCTTGAGGCATGT 63 + ILLUMINA 0.276053492 234 FALSE ACP1 +snp_rs10215963 snp_rs10215963 snp_rs10215963 Homo sapiens hg19 chr7 26583700 26583771 + AAACATGGAGGCAAGTCAAGAAGCCA 66 AAGGCAGAGCATGCAGCTGTGATTTT 89 + ILLUMINA 0.512636745 213 FALSE ACP1 +snp_rs11265625 snp_rs11265625 snp_rs11265625 Homo sapiens hg19 chr1 153642830 153642884 + ATCATCTTAGGTTGGCTACTTTCATCC 39 ACACTTAATAACCCATAATCCTGGGCC 42 + ILLUMINA 0.833189513 196 FALSE ACP1 +snp_rs10489391 snp_rs10489391 snp_rs10489391 Homo sapiens hg19 chr1 210458767 210458832 + CGCCTTCCCAGGTAGAATTTCCTGTTT 64 GAGAACCAAGCAGCTAAGCTTGTCCTA 32 + ILLUMINA 0.766603308 207 FALSE ACP1 +snp_rs11024021 snp_rs11024021 snp_rs11024021 Homo sapiens hg19 chr11 16735412 16735495 + TTCCACTCCTGCAGAACTCAAATCAG 71 GCTAGAAAATATAACCTCCATCATGAACC 77 + ILLUMINA 0.315235357 225 FALSE ACP1 +snp_rs1034826 snp_rs1034826 snp_rs1034826 Homo sapiens hg19 chr7 108083526 108083592 + CACGGAAAGAACATATTCACCAGGAG 50 TGTCACAGTTCATTAAATGCCATACAC 86 + ILLUMINA 0.547197949 208 FALSE ACP1 +snp_rs10901226 snp_rs10901226 snp_rs10901226 Homo sapiens hg19 chr9 133483134 133483189 + GCCCCTGATCTAACTGCTGGTTTTCAT 40 TTGAACCTGATTTCCTCTCAGTGATGC 82 + ILLUMINA 0.793738181 197 FALSE ACP1 +snp_rs10997716 snp_rs10997716 snp_rs10997716 Homo sapiens hg19 chr10 53235938 53236016 + AGGTGGGTTGCATAACTCTTTGCTTTC 40 CACTGTGAAGGTGACAATAGATCCTAG 61 + ILLUMINA 0.603111114 220 FALSE ACP1 +snp_rs10739688 snp_rs10739688 snp_rs10739688 Homo sapiens hg19 chr9 129772417 129772480 + CACCGTGCTGAAGGGCTGTGAGAGTA 44 CTCTTTGTCCTTCCTCATCGCTTTCT 68 + ILLUMINA 0.58712508 205 FALSE ACP1 +snp_rs10903900 snp_rs10903900 snp_rs10903900 Homo sapiens hg19 chr10 2990174 2990231 + ATGCACAGGCCTCTAATTCAGTGCCTA 51 CTTAGTGGGCAGCAGACTTCCTAAGATA 53 + ILLUMINA 0.846296245 199 FALSE ACP1 +snp_rs10192459 snp_rs10192459 snp_rs10192459 Homo sapiens hg19 chr2 152517899 152517957 + CCTTTCAAGGAGGTTGAGCTCCACAAA 32 TTTCTCATTTTGATCCACCAGTGCTGC 54 + ILLUMINA 0.818877583 200 FALSE ACP1 +snp_rs10860066 snp_rs10860066 snp_rs10860066 Homo sapiens hg19 chr12 97073187 97073274 + ATTGGCAAGATCTAAAGTTATTTGCAT 89 CTCTTACCTTGGCTTGGTGCAGCATTT 32 + ILLUMINA 0.276871149 229 FALSE ACP1 +snp_rs10184780 snp_rs10184780 snp_rs10184780 Homo sapiens hg19 chr2 20054313 20054360 + GACATCAGGAAGAAGGGCAAGCCAA 65 AATGAGGAAACATTGCAGAGACGAACC 63 + ILLUMINA 0.757362025 189 FALSE ACP1 +snp_rs11152428 snp_rs11152428 snp_rs11152428 Homo sapiens hg19 chr18 61994612 61994684 + ATGTGTTTCCTGGGCCACTATTGCCTT 76 CAGTGTCTACCATCCGTGTAGAATCTAC 29 + ILLUMINA 0.592283456 214 FALSE ACP1 +snp_rs10925402 snp_rs10925402 snp_rs10925402 Homo sapiens hg19 chr1 237559370 237559419 + ATGGGAATCTGCATACAAATGCTATTG 70 TTGTTATCTGCCAGCAATTAGGGGC 34 + ILLUMINA 0.682003484 191 FALSE ACP1 +snp_rs10111409 snp_rs10111409 snp_rs10111409 Homo sapiens hg19 chr8 133118395 133118452 + GATAACTGTACAGTCTTTCTGTGTAGG 51 AAATGTTGCAGGAAGGGAACATCCTC 71 + ILLUMINA 0.776424516 199 FALSE ACP1 +snp_rs1011539 snp_rs1011539 snp_rs1011539 Homo sapiens hg19 chr7 14294504 14294567 + ATAGAACCCATCTGAGATTTTTCCTCT 56 CAGTAGAAGTTGGAGGAAGTCCCACAT 53 + ILLUMINA 0.706305186 205 FALSE ACP1 +snp_rs11084990 snp_rs11084990 snp_rs11084990 Homo sapiens hg19 chr19 3009141 3009191 + CTCTGCCTGTCACACTACAGATGAGA 60 CCCTCCCAGGACAAATCTGGTCCACT 53 + ILLUMINA 0.727336284 192 FALSE ACP1 +snp_rs10122609 snp_rs10122609 snp_rs10122609 Homo sapiens hg19 chr9 9283465 9283525 + CCCATCTACAAATGAACCCTTTACAGG 41 GTGTTCCTCAAAGCTATCTGCTTAGT 59 + ILLUMINA 0.766564094 202 FALSE ACP1 +snp_rs10208207 snp_rs10208207 snp_rs10208207 Homo sapiens hg19 chr2 169074864 169074941 + TAGACAAGTAACTTGTAAAGAACCACA 57 GTATTTGCGTCAACTGCTCTCCCACTT 36 + ILLUMINA 0.42061045 219 FALSE ACP1 +snp_rs10954365 snp_rs10954365 snp_rs10954365 Homo sapiens hg19 chr7 131855080 131855137 + GCACACAGCACCAAAAAGGTAGGTTT 50 GGTATGAAAAGCTGATGCACATCCCA 50 + ILLUMINA 0.828650396 199 FALSE ACP1 +snp_rs11118109 snp_rs11118109 snp_rs11118109 Homo sapiens hg19 chr1 218632844 218632891 + ATAGAATCATTAAACCACATCAATAACCC 94 TGACTTTCTGAAGAGCCACGGGGT 25 + ILLUMINA 0.36085074 189 FALSE ACP1 +snp_rs10168253 snp_rs10168253 snp_rs10168253 Homo sapiens hg19 chr2 180659495 180659545 + CCAACATCCACTTGTCCATAACTTTAGG 40 CAGAGAGAGGTTATGGGTGGAGATACA 56 + ILLUMINA 0.86511403 192 FALSE ACP1 +snp_rs11118515 snp_rs11118515 snp_rs11118515 Homo sapiens hg19 chr1 220473942 220474020 + CAGCACAATAACAGCAAGCTCTGTGT 53 AGCAGAGGAAAACCAAAGCTACGTG 73 + ILLUMINA 0.427139255 220 FALSE ACP1 +snp_rs10133359 snp_rs10133359 snp_rs10133359 Homo sapiens hg19 chr14 26719062 26719120 + AATTCAGCTACCTTAAAATGGCAAAAA 108 TCAGAGTAGTGTTTCATGTCTGAGTCC 70 + ILLUMINA 0.428648445 200 FALSE ACP1 +snp_rs1038024 snp_rs1038024 snp_rs1038024 Homo sapiens hg19 chr17 25725521 25725573 + AGAGACACCTGCCCTGGATGAGGGAAA 74 ATGTCCTCAGAGATGGTCAGCCCTCTA 62 + ILLUMINA 0.717145517 194 FALSE ACP1 +snp_rs11144978 snp_rs11144978 snp_rs11144978 Homo sapiens hg19 chr9 79225247 79225297 + GATCCACAGTGCCCCAACACAGCTTTT 50 CCTACCCTTACCCAAATGAGTGTGTT 48 + ILLUMINA 0.866855188 192 FALSE ACP1 +snp_rs10932037 snp_rs10932037 snp_rs10932037 Homo sapiens hg19 chr2 204825261 204825327 + TAGGAAACATTGCCCGGAATTGAAAGC 20 TAGCCTGAAAGCTGCAGTTACTATAGG 70 + ILLUMINA 0.699317955 208 FALSE ACP1 +snp_rs11114607 snp_rs11114607 snp_rs11114607 Homo sapiens hg19 chr12 81157358 81157422 + AAAATGTGCCAATGAGTAAACTGAGTC 89 AATTCCAGGGAGTAGACGGTAAATTGG 26 + ILLUMINA 0.55385638 206 FALSE ACP1 +snp_rs10058793 snp_rs10058793 snp_rs10058793 Homo sapiens hg19 chr5 4739730 4739790 + GTCTGAATAATTTTAACCAGTACAAATGTG 145 CTTACATCATCAGCTGAGGAGATTTCC 103 + ILLUMINA 0.150583045 202 FALSE ACP1 +snp_rs11017093 snp_rs11017093 snp_rs11017093 Homo sapiens hg19 chr10 131926021 131926095 + TAACATGTGGAGGGCTTTTCCTCTCT 50 GCATCGGTTTGTGTGAATTCTCAGCT 70 + ILLUMINA 0.598415367 216 FALSE ACP1 +snp_rs1015077 snp_rs1015077 snp_rs1015077 Homo sapiens hg19 chr6 167526427 167526503 + AGAGAATTCTTGATGCTGCAATGCATC 56 CTTCTCTAATTAAACATCTGAACCCTCTG 94 + ILLUMINA 0.373943811 218 FALSE ACP1 +snp_rs12785223 snp_rs12785223 snp_rs12785223 Homo sapiens hg19 chr10 104843932 104843991 + AGGGACCCTCTGTGATCCATTCCTAAA 66 CTTACACTTGTTCTGTGGATGGAGACA 90 + ILLUMINA 0.690399979 201 FALSE ACP1 +snp_rs10745558 snp_rs10745558 snp_rs10745558 Homo sapiens hg19 chr12 91910096 91910153 + GAGTTTAATTACCTATCCAAGGTCACCC 90 CCACCTATTTAATTCCTGTGTGTAGCT 75 + ILLUMINA 0.650857282 199 FALSE ACP1 +snp_rs10499441 snp_rs10499441 snp_rs10499441 Homo sapiens hg19 chr7 14505603 14505683 + GCTGGTGTACACAATTATTGAGACTTTC 50 GGTTAAATAAGGCAGGAGTTGTCAGTG 67 + ILLUMINA 0.569239643 222 FALSE ACP1 +snp_rs11137287 snp_rs11137287 snp_rs11137287 Homo sapiens hg19 chr9 140382627 140382694 + CTCCTCATCCTGAGCTTCGGCCTGAA 42 TGCAGCTTTTCCTTGGGAATCCCTTT 82 + ILLUMINA 0.492813933 209 FALSE ACP1 +snp_rs10489858 snp_rs10489858 snp_rs10489858 Homo sapiens hg19 chr1 19947170 19947225 + GCTGGTCTGAACTGTTGATTCTTACTTC 47 TTAGCAATGGAGTCGGCATCATTCTTG 30 + ILLUMINA 0.843030306 197 FALSE ACP1 +snp_rs10519980 snp_rs10519980 snp_rs10519980 Homo sapiens hg19 chr4 149634927 149634994 + GGAAACTGAGAACAAGGGAGGTAAAAA 124 AAGAACGGAAACATGATGGGCAGTAAG 48 + ILLUMINA 0.403291967 209 FALSE ACP1 +snp_rs10489924 snp_rs10489924 snp_rs10489924 Homo sapiens hg19 chr1 99458893 99458959 + GCATGTTCTCTTTCACACTGGATTCAC 76 GGAAATAAAGATCTCTTTGTGAAAGACC 137 + ILLUMINA 0.284522685 208 FALSE ACP1 +snp_rs11081675 snp_rs11081675 snp_rs11081675 Homo sapiens hg19 chr18 28580599 28580647 + ATTCTCTTCTCTAACACCGAACTTGT 75 CTCTTCACTTTCAAACCCTTCTTATTC 107 + ILLUMINA 0.490922718 190 FALSE ACP1 +snp_rs10183112 snp_rs10183112 snp_rs10183112 Homo sapiens hg19 chr2 38445683 38445747 + ATGTTTAGGAGGAGTCAGGGACAAATC 61 GAGAGGCTTTGCAGTTTGAGCTGTTA 73 + ILLUMINA 0.716638475 206 FALSE ACP1 +snp_rs10817727 snp_rs10817727 snp_rs10817727 Homo sapiens hg19 chr9 117979331 117979385 + ATCAGAAGCGTGAAACGGACTAATACG 35 CTGCTTGTGTAGTTAGCCTATTTCACA 54 + ILLUMINA 0.8541048 196 FALSE ACP1 +snp_rs10440685 snp_rs10440685 snp_rs10440685 Homo sapiens hg19 chr5 77182996 77183058 + ACCTAGACAATAGTGGCATACAAAGAA 44 GTCGCTATCAACTCAGATTTTCGAGTTG 34 + ILLUMINA 0.695041264 204 FALSE ACP1 +snp_rs10486239 snp_rs10486239 snp_rs10486239 Homo sapiens hg19 chr7 8584147 8584215 + ACATAGATCACAGATTCTTGAAAGACTC 66 TTTGATTTTACGGCTTTTGTATTTGTATG 180 + ILLUMINA 0.070576858 210 FALSE ACP1 +snp_rs10505770 snp_rs10505770 snp_rs10505770 Homo sapiens hg19 chr12 13025970 13026035 + TGAAAGGATCTGCTCTAATCTCTTCGC 52 ACTTCTGTGTTCAATGCATTGCTCCTC 73 + ILLUMINA 0.761045033 207 FALSE ACP1 +snp_rs10223664 snp_rs10223664 snp_rs10223664 Homo sapiens hg19 chr6 98677619 98677666 + CCTCTGAGGCCTAATGAGTTTGATATG 44 GGCAAAGTATGACCTGGACTGAAAGT 47 + ILLUMINA 0.884733962 189 FALSE ACP1 +snp_rs10490026 snp_rs10490026 snp_rs10490026 Homo sapiens hg19 chr2 210733351 210733419 + GCCTCACTTTCATAAAGGAAGTATTCA 109 CTGTAACCCATGCAGAGAACACCTCATA 54 + ILLUMINA 0.478788627 210 FALSE ACP1 +snp_rs10514527 snp_rs10514527 snp_rs10514527 Homo sapiens hg19 chr16 82137560 82137626 + TGATTCATTGCTGGACACAACATCACC 53 ACAAAAAGCACACACTTCCATGTTGA 91 + ILLUMINA 0.573918816 208 FALSE ACP1 +snp_rs10744146 snp_rs10744146 snp_rs10744146 Homo sapiens hg19 chr12 17212795 17212852 + GTTGTTTCTAAGGGTACTTCACTGAGG 36 TGCAAGGTCGTGAACAAGGGTGAGATT 40 + ILLUMINA 0.864419706 199 FALSE ACP1 +snp_rs10845745 snp_rs10845745 snp_rs10845745 Homo sapiens hg19 chr12 13466271 13466320 + TGAATTCTCAACACTAGAAGGAGAGCC 48 CAGGGCAAAGCTGTTTTTGACACAAC 77 + ILLUMINA 0.846311749 191 FALSE ACP1 +snp_rs1032886 snp_rs1032886 snp_rs1032886 Homo sapiens hg19 chr12 44528973 44529031 + CTCCAACAATCACTGGGTTATTTTCTC 47 CAGGCACTGAGTGATAATCCAAGATGG 47 + ILLUMINA 0.863052801 200 FALSE ACP1 +snp_rs10487449 snp_rs10487449 snp_rs10487449 Homo sapiens hg19 chr7 126071986 126072057 + ATCTGGTCTTGTGATGTGCATGGGTA 47 GAAATGCTGACATCAACAACCAAATCG 76 + ILLUMINA 0.573763678 213 FALSE ACP1 +snp_rs10813205 snp_rs10813205 snp_rs10813205 Homo sapiens hg19 chr9 29943550 29943631 + AGAACAGTGATGTGGTTATATCTAAATTG 71 GGAGGTTGGGGGCAGTTAAAACTCTTT 50 + ILLUMINA 0.408130054 223 FALSE ACP1 +snp_rs1003346 snp_rs1003346 snp_rs1003346 Homo sapiens hg19 chr9 111815247 111815310 + TTAGATTGGTAGTCTCCAACAACAAAA 32 CACAATAGCAAGGCCCATGAAACTCT 47 + ILLUMINA 0.650790299 205 FALSE ACP1 +snp_rs11185125 snp_rs11185125 snp_rs11185125 Homo sapiens hg19 chr1 108061566 108061615 + GCCATCTTTCTGGCATGATCTCCCATTA 54 TTCTCCAGTTAAGTCCTACAGATTTTT 86 + ILLUMINA 0.624482576 191 FALSE ACP1 +snp_rs11073674 snp_rs11073674 snp_rs11073674 Homo sapiens hg19 chr15 87361895 87361952 + AGAGAACTAATATGGGAGCATATCACC 43 GTAATTTTGGAACCAGACACCAATGGG 60 + ILLUMINA 0.823405187 199 FALSE ACP1 +snp_rs10187631 snp_rs10187631 snp_rs10187631 Homo sapiens hg19 chr2 120343750 120343817 + GATGGGGTGAGGGCTCAGAAGGTAT 79 CCCAGCACTGCACAGGATGTAGAATTA 64 + ILLUMINA 0.550731548 209 FALSE ACP1 +snp_rs11125812 snp_rs11125812 snp_rs11125812 Homo sapiens hg19 chr2 59989528 59989602 + CAGGGTAATAAGAAAACCCATTGCAGA 68 CAGTTTTTGACTTTGATTTCCGAGTCC 66 + ILLUMINA 0.654042033 216 FALSE ACP1 +snp_rs10837327 snp_rs10837327 snp_rs10837327 Homo sapiens hg19 chr11 40082709 40082775 + ACTGAAAGAGATAGAATCCTTGCCT 72 AAGCATGCTCTGAATTCTTCTTAGGT 87 + ILLUMINA 0.477712155 208 FALSE ACP1 +snp_rs10937470 snp_rs10937470 snp_rs10937470 Homo sapiens hg19 chr3 191000726 191000784 + GAATTTAATTAATTCAAAGCTGGCAAATG 167 CCCAAAAGACTTTGGATGTATCCACTC 59 + ILLUMINA 0.128492085 200 FALSE ACP1 +snp_rs10510060 snp_rs10510060 snp_rs10510060 Homo sapiens hg19 chr10 121863392 121863443 + TCTTAGTTGCTGTGAGGCTCTAGACA 48 GCTCCTCCCAGCTTGAAGTAGCATGAA 55 + ILLUMINA 0.841175985 193 FALSE ACP1 +snp_rs10871565 snp_rs10871565 snp_rs10871565 Homo sapiens hg19 chr18 75698271 75698320 + AACTTTCTATCTGTCTGCCAATTACCT 76 ATTTCCCCTCACGAAAATTAACATCAG 59 + ILLUMINA 0.678949414 191 FALSE ACP1 +snp_rs10950049 snp_rs10950049 snp_rs10950049 Homo sapiens hg19 chr7 66230777 66230827 + CGACTTAGTCCCATTTCCAAAACTCG 56 TGCTAGGCAGACTTCCCAAACTATGT 51 + ILLUMINA 0.853960602 192 FALSE ACP1 +snp_rs10816943 snp_rs10816943 snp_rs10816943 Homo sapiens hg19 chr9 112983736 112983790 + TTTCGGCATTTAATTTGGCCCTTTCTG 48 TGGGTTCTCTGGATAGAGACAGACCT 72 + ILLUMINA 0.816934363 196 FALSE ACP1 +snp_rs10512393 snp_rs10512393 snp_rs10512393 Homo sapiens hg19 chr9 112153077 112153128 + TTTTGGCTTATATGTACAGAGGAGGTT 72 CAGAACAAGTCTGGTCCCATCTTCTGT 52 + ILLUMINA 0.771009234 193 FALSE ACP1 +snp_rs10511942 snp_rs10511942 snp_rs10511942 Homo sapiens hg19 chr9 37702789 37702848 + GGTGGTGGGGAATTATTAGGAGGAGAA 42 TGTTTGGTTTATCTATTCCCTATCGGG 54 + ILLUMINA 0.832865527 201 FALSE ACP1 +snp_rs10240790 snp_rs10240790 snp_rs10240790 Homo sapiens hg19 chr7 89880864 89880915 + GGTTGTTGGCCAGAGTTATTTTGTCAC 54 CACACCTAGCACAATTCCTGAAACA 183 + ILLUMINA 0.140378825 193 FALSE ACP1 +snp_rs1147199 snp_rs1147199 snp_rs1147199 Homo sapiens hg19 chr9 87275809 87275872 + TATCAGCCTTTGGTTCCATGTGACCT 55 GTGAACATGCTTGTAGATTCTGTTCCT 62 + ILLUMINA 0.769709012 205 FALSE ACP1 +snp_rs1058326 snp_rs1058326 snp_rs1058326 Homo sapiens hg19 chr9 27446989 27447063 + GAGCATCCCATTTATTAAGGGGAAAAT 61 GAATCACTTTCCACACATGGGGGTGTA 42 + ILLUMINA 0.611393781 216 FALSE ACP1 +snp_rs10484820 snp_rs10484820 snp_rs10484820 Homo sapiens hg19 chr6 139858182 139858274 + CTTGATGGGCTTCTTCTGGGAAAACA 64 TGCTGGTCCAAGGTGCCTCTTGCTGTT 47 + ILLUMINA 0.344041341 234 FALSE ACP1 +snp_rs10829531 snp_rs10829531 snp_rs10829531 Homo sapiens hg19 chr10 130761863 130761919 + CAGGTCTCGAAAAGGAATTTGGGGGAA 75 GACCAGAAGGATGAAACCAAGCCAAT 73 + ILLUMINA 0.810076622 198 FALSE ACP1 +snp_rs10835211 snp_rs10835211 snp_rs10835211 Homo sapiens hg19 chr11 27701279 27701333 + GGCCAACTTTGCATGGTTAATCATTTAG 54 AGCTGAAAGTCAGAACCAGCTGTGTT 72 + ILLUMINA 0.755395475 196 FALSE ACP1 +snp_rs10160742 snp_rs10160742 snp_rs10160742 Homo sapiens hg19 chr11 115239304 115239365 + ACATGAGAGCCTTTGTAAGAACCTGAA 55 TGACTCTGAGACTAAAAACACTACTAC 70 + ILLUMINA 0.659815518 203 FALSE ACP1 +snp_rs10512461 snp_rs10512461 snp_rs10512461 Homo sapiens hg19 chr17 32475304 32475365 + TTTAGGAACTTGTGCAGTAGCTTCAGT 41 CCCAAACGGAGGCTGACATTATGGAAA 80 + ILLUMINA 0.70048694 203 FALSE ACP1 +snp_rs10869031 snp_rs10869031 snp_rs10869031 Homo sapiens hg19 chr9 74130207 74130257 + TTCCTTGAAGCCCTACAAGTGCAGCAT 48 GTTGGGCATCAGCATAGTCAATAGAGG 49 + ILLUMINA 0.894520192 192 FALSE ACP1 +snp_rs1055010 snp_rs1055010 snp_rs1055010 Homo sapiens hg19 chr7 29551021 29551096 + GTATCACATCTGGCTTTCAATTAGCTG 66 GACTTAAGAGGAAACTGTGGGCACTT 68 + ILLUMINA 0.555126879 217 FALSE ACP1 +snp_rs10930486 snp_rs10930486 snp_rs10930486 Homo sapiens hg19 chr2 172472487 172472552 + GTGCAATCTTGTCTATTTGAGTAATGG 57 GTTGGAGGAAGGGCATAACATAGAGGT 53 + ILLUMINA 0.660436714 207 FALSE ACP1 +snp_rs1052448 snp_rs1052448 snp_rs1052448 Homo sapiens hg19 chr9 18927931 18928009 + TAGCCGGTGATTAAATGTCATTTTCCC 58 GCTAACACTTCCAACTCCCTCTGGTT 60 + ILLUMINA 0.510605867 220 FALSE ACP1 +snp_rs10488735 snp_rs10488735 snp_rs10488735 Homo sapiens hg19 chr11 34438475 34438526 + TCTGACTTGGTGCAGATAGACTTCAAG 44 GCAAGTAAAGGGAACACATGTGGACA 75 + ILLUMINA 0.883724256 193 FALSE ACP1 +snp_rs10255854 snp_rs10255854 snp_rs10255854 Homo sapiens hg19 chr7 38959746 38959822 + GCATACCCAGAAGAACCCAAGAAAGA 54 CCCCCACCTTTACCCCAATGCCCACT 35 + ILLUMINA 0.46651904 218 FALSE ACP1 +snp_rs10961084 snp_rs10961084 snp_rs10961084 Homo sapiens hg19 chr9 13484950 13485006 + GGGGAAGAACACATTCTATACACTTGA 62 GACCAAACAGACTTAACTGCAGGCCT 53 + ILLUMINA 0.803983292 198 FALSE ACP1 +snp_rs10189774 snp_rs10189774 snp_rs10189774 Homo sapiens hg19 chr2 171375418 171375468 + CTTCAGGTTGAATTAAAGTTCAGTGGA 62 ACAGTTAATCCTAGCCACATCATCACA 60 + ILLUMINA 0.76321132 192 FALSE ACP1 +snp_rs10893306 snp_rs10893306 snp_rs10893306 Homo sapiens hg19 chr11 124813437 124813483 + TCCTACCAAAGAGGGAGGCTCAGAAAT 70 GGATCCCTGTCTAGGAGCTGAAATAT 72 + ILLUMINA 0.812343212 188 FALSE ACP1 +snp_rs1106944 snp_rs1106944 snp_rs1106944 Homo sapiens hg19 chr11 126008190 126008251 + GAACTCAGTTCACAGGAACACATATGA 67 GCCCTAACAAGTAAGTCCTCCTTGATC 37 + ILLUMINA 0.775830757 203 FALSE ACP1 +snp_rs1055352 snp_rs1055352 snp_rs1055352 Homo sapiens hg19 chr9 128910339 128910385 + AGAAAGCTAACTTAGAACCACTCCTTGG 42 CTTCGGGCACCTTGTTGGTTTGCA 24 + ILLUMINA 0.594162219 188 FALSE ACP1 +snp_rs10141526 snp_rs10141526 snp_rs10141526 Homo sapiens hg19 chr14 62303171 62303231 + GCAGTCCATTCACTTGAAAGGCATTTG 42 TTTCTACTCCACCTCCCATTGATTTGC 69 + ILLUMINA 0.803812655 202 FALSE ACP1 +snp_rs10094093 snp_rs10094093 snp_rs10094093 Homo sapiens hg19 chr8 4505832 4505882 + CTTTGCCCACTTTTTGATGGGGTTGT 1200 CTCAGCCATGAGTCTTGGGGCTCAGT 40 + ILLUMINA 2.67E-58 192 FALSE ACP1 +snp_rs11009888 snp_rs11009888 snp_rs11009888 Homo sapiens hg19 chr10 35008018 35008068 + GGAAACAGCCTAGAAACAATACACTCC 75 TAGTGCTCGAATCCTAACCTTCATGTC 39 + ILLUMINA 0.841622465 192 FALSE ACP1 +snp_rs11082351 snp_rs11082351 snp_rs11082351 Homo sapiens hg19 chr18 41484259 41484312 + ACTTTTGTCTACTTGACCCATCAAGAC 53 TCTGACTACATAGGCTTGTATGAAAAT 70 + ILLUMINA 0.682308703 195 FALSE ACP1 +snp_rs1113272 snp_rs1113272 snp_rs1113272 Homo sapiens hg19 chr4 165646689 165646762 + TTCCTTATGCATTGCAGGCTGGACAA 60 AAAACCCAAATTTCAGGAGCACATCAT 80 + ILLUMINA 0.570563977 215 FALSE ACP1 +snp_rs10250461 snp_rs10250461 snp_rs10250461 Homo sapiens hg19 chr7 22289272 22289337 + TGACTCTCCACCAAACAAAGCTTGGT 55 AGCTCATTCCCTAACTCTGCGGGTCATA 21 + ILLUMINA 0.676202224 207 FALSE ACP1 +snp_rs11143230 snp_rs11143230 snp_rs11143230 Homo sapiens hg19 chr9 74887624 74887687 + CACATACATGATTCAAACCACACAGCT 67 GAATCTCAGGTTTGGAAGGGCACTCTA 66 + ILLUMINA 0.709387958 205 FALSE ACP1 +snp_rs10520689 snp_rs10520689 snp_rs10520689 Homo sapiens hg19 chr15 90950279 90950338 + GGACTAATCAGAGGCTTCCTGAAATTG 61 AATCAGTGGGTGTTGGTTGTCCATTAG 44 + ILLUMINA 0.842056616 201 FALSE ACP1 +snp_rs11079784 snp_rs11079784 snp_rs11079784 Homo sapiens hg19 chr17 45702187 45702248 + GATTTTCCTGCACTCTGTCCATGTCT 50 TCCCTATCATAAGTCATACACCCATTT 25 + ILLUMINA 0.65022705 203 FALSE ACP1 +snp_rs11632663 snp_rs11632663 snp_rs11632663 Homo sapiens hg19 chr15 27564707 27564752 + TGTGATACGGCAGTTGAAGACATAGAG 18 GGCGTGGGCAGAGCACAAATGGGAT 45 + ILLUMINA 0.615586207 187 FALSE ACP1 +snp_rs10079889 snp_rs10079889 snp_rs10079889 Homo sapiens hg19 chr5 32975406 32975462 + CCCTCCTAACACTTTTCTGCTGCAGAA 59 GGCAGTACTTACAAAGTTAGACTTTGT 73 + ILLUMINA 0.745322966 198 FALSE ACP1 +snp_rs10504373 snp_rs10504373 snp_rs10504373 Homo sapiens hg19 chr8 65107845 65107907 + ATGACAGTTTGGTTTAAATAATATGCAAC 191 GGTTTCCTTTCTTAAGTCAGCATACAT 76 + ILLUMINA 0.056308824 204 FALSE ACP1 +snp_rs1160382 snp_rs1160382 snp_rs1160382 Homo sapiens hg19 chr7 149279913 149279967 + CTTTTGTCCTCAGGAATGTCAAACACC 81 ACTCTACTCACTGCAGCTCTCAAGGT 78 + ILLUMINA 0.708279308 196 FALSE ACP1 +snp_rs10887788 snp_rs10887788 snp_rs10887788 Homo sapiens hg19 chr10 89898673 89898732 + GAGAAGGTAAGTTTACAACAGAATGGA 50 CTAGCTCAGTGGTCCTTACACTTAAAC 68 + ILLUMINA 0.747188108 201 FALSE ACP1 +snp_rs10257539 snp_rs10257539 snp_rs10257539 Homo sapiens hg19 chr7 135439817 135439884 + GATCTCTTCTGCATTGGGTTCTCTGCT 59 CCCTCTTTGGTTGACTTCATTCATGG 83 + ILLUMINA 0.630070627 209 FALSE ACP1 +snp_rs11002633 snp_rs11002633 snp_rs11002633 Homo sapiens hg19 chr10 80447690 80447755 + GGTGCAGTCAGTAAAGCATGTGTGCTA 32 TGTGTGCATACATACAAGGGTGTGTG 67 + ILLUMINA 0.679364651 207 FALSE ACP1 +snp_rs1058932 snp_rs1058932 snp_rs1058932 Homo sapiens hg19 chr10 96796783 96796829 + TATTTGTGCAGTGACCTGAACAACTC 71 GGCTAGCATTCTTCAGACAGGGATGAA 74 + ILLUMINA 0.785343458 188 FALSE ACP1 +snp_rs11063356 snp_rs11063356 snp_rs11063356 Homo sapiens hg19 chr12 4938515 4938572 + AAAGCATGTCTGTACTTACCGTCTGAG 28 TTGCCAGGACCCCTTGAAATTTTG 68 + ILLUMINA 0.590490431 199 FALSE ACP1 +snp_rs1016726 snp_rs1016726 snp_rs1016726 Homo sapiens hg19 chr7 29356325 29356372 + GTTTTCAGGTAGAGTTGAATGTAGCT 57 GTCCAGATAATCTTGGTATAGTCTCCT 36 + ILLUMINA 0.777651511 189 FALSE ACP1 +snp_rs10875815 snp_rs10875815 snp_rs10875815 Homo sapiens hg19 chr12 48834246 48834297 + GACCATGATAATTTTAGTCCACATGCC 57 TACCATTTCTACAGCATTATTAGGGCC 59 + ILLUMINA 0.850910101 193 FALSE ACP1 +snp_rs10957982 snp_rs10957982 snp_rs10957982 Homo sapiens hg19 chr8 81455678 81455739 + GGTGTTTCTCCCAGCTGGTAAAGAGAA 57 GATTTTCAAAGAGGGCATCAGCATCAC 83 + ILLUMINA 0.785543235 203 FALSE ACP1 +snp_rs1258540 snp_rs1258540 snp_rs1258540 Homo sapiens hg19 chr7 63109190 63109244 + ATGTTCAAACAGAGTGGCCTGTTCAG 48 TGAGGATGTCAACTGAGGAGGGGCAT 53 + ILLUMINA 0.784289176 196 FALSE ACP1 +snp_rs10087078 snp_rs10087078 snp_rs10087078 Homo sapiens hg19 chr8 8930658 8930710 + GAACAAATGCATAATCCTTCATCTGGC 68 ACCACCACATAGTAGCATTAATCTGTC 63 + ILLUMINA 0.796318253 194 FALSE ACP1 +snp_rs1050190 snp_rs1050190 snp_rs1050190 Homo sapiens hg19 chr3 141644727 141644782 + CATGACATTGGGTTACATCATAACGTGC 60 GTGGTTTAATTGCCAAGTGTCTAAAGC 63 + ILLUMINA 0.801391454 197 FALSE ACP1 + +[Targets] +TargetA TargetB Target Number Chromosome Start Position End Position Probe Strand Sequence Species Build ID +snp_rs10138962 snp_rs10138962 1 chr14 104995748 104995938 - CCACCACATCCAGCCTCTACTAATGTCATTTGTAGCCTTTGTAGCACCCTTTCCCTCTCAAACTTGAGCACTTTTTAGAGCAAGAGTTTGCTATGGACAACTATGCTGGTGATGCAGGACAGGCAAGCCGCAAAGTGGGGCTC Homo sapiens hg19 +snp_rs1149580 snp_rs1149580 1 chr11 76549360 76549559 - GCCAAGCACAAAGCAGCCACCGGCAAAGCTTTTTTAAAGAGAAGAACAGACACATTGAGTTTGCACATTTGAAGCCAGGGCCAGAACTTATTTCCTGCCACCCTGATGGTAACAAAGATGCATTTTGCACTGTGCTGGGCTGTCAG Homo sapiens hg19 +snp_rs10988298 snp_rs10988298 1 chr9 132042345 132042541 - ACCTGGGATGTATAGATGAAATTTGTATAGGTGGTCGCAGTTATTACTATTATTATTATTATTTACAGACAGGATCTTGCTCTGTCACCCAAGCTGGAGGGCAGTGGCACCATCACAGCTCACTGCAGCCTCAACCTCCTGGG Homo sapiens hg19 +snp_rs10086550 snp_rs10086550 1 chr8 143362875 143363074 - GGGTTGCCCTTGGCTTCCCTAGAGAGGTCCTCACCATGAGGTCTAAAAGCTCTGGGTCCCCTTAACCCTGACCCTAACCCTGGGGTGACTGTGTCCAGTTCTGACTCCATGCGCTGTGGCCTCCTCTGCTTGTGGAGAGCCAGAGTCTCTC Homo sapiens hg19 +snp_rs10409978 snp_rs10409978 1 chr19 57796523 57796716 - AGGGAAGCCAGCACCAGACAACCAGTATTAGTGCCACAGGGGGGCCTGGCTGCAAATCCTGCCTTTGGGTTCTACAAAACATCCCATTTCCTGGTAACACATCCCTCTCCTTTGGCTGTGACCAAAAGCAAACTATATTT Homo sapiens hg19 +snp_rs1060493 snp_rs1060493 1 chr15 31516299 31516546 - GCCCTCTCCCAGAGCCGGTGGCCTGCGTGCCAGGTCCCCGACAAATGCTGGCTCCATGGCAGCTGCGATGACTTCCCTCGAGAAGTGCCAGTCCGCAGGGCAATCTCGAGGTCCTCGTGCGGGTGACCAGCTGCGGCACGGCCAGCACGGCACAGGGAGGGAGGGGCTGTGCTGACCCTCAGGTGTCTCGCGGGGGCCC Homo sapiens hg19 +snp_rs12777222 snp_rs12777222 1 chr10 35387802 35388000 - TTTCTGTGAATTAGCTTCCCTCCAGACTTACCACATTTGACTTGTTCGCTTTCTTTGTTCCTATCTTCTCAAATGAGATGGCCTATATTACTTATTTAATTTATTTATTTCGAGACAGAGTCTTGCTTTGTTGCCCAGGCTGGA Homo sapiens hg19 +snp_rs12563211 snp_rs12563211 1 chr1 34486048 34486289 - AAAAATCAGTCTGGTTCCAAAGCCCACACTCTCCACCGTGTTCCTGCTGAAAATAAGCCCTGCACAGTTCTCCAGGCCTGCCCCACTCGCCTACCCCTACCCCACAGCAGGAGAGGCCTGGGAGAGTCGGGTGGGCCAGCAGCATGACGCTGGGGCATCTCCTTGAGCCTGTGGTCCCCAGCCCTGGCC Homo sapiens hg19 +snp_rs10843013 snp_rs10843013 1 chr12 28025030 28025244 - TTCAAGTACTTCTGTGCTAGTTAAAACTGGTACTGCTCTATCCAACAACACTAAGTACAAAATCTTACCGCTTTTGTCAAAGTGAAAAATGTTTCCAGGAAAAAAGAAAAAAGCCTTTTAAGTTTGGATGAACCTTTATTTCTAATTATATGGCTTTCAAA Homo sapiens hg19 +snp_rs12678837 snp_rs12678837 1 chr8 22950234 22950426 - GGAAGGGTTGACGGAGAAAAAGTGAAGGTCCGCCCAGGGTTGGAGGAAGCCACAGGAGAGGGACCATAGGACTCCCCCAGAACCAGGACTTCCCCAGAAACCAGGGCCAGTTCACCACTCAGGGACCCACTGCCTCTTCCC Homo sapiens hg19 +snp_rs10954737 snp_rs10954737 1 chr7 83532864 83533108 - ATTTAAAGATCTCCCTCCCAATGGGAGATGCAGACATACCCATTTATTATCACAGGCATCCACAGTGTAGTTGTTCAACCAAACACACACACACACACGCACACACACATTTACATACACCCTTTCCAAGAGAAAAAATACTAATTTTTAAAGACAATGTAATTTTAATACAAAATGAAAAAGAAGCAAATA Homo sapiens hg19 +snp_rs11100509 snp_rs11100509 1 chr4 164478714 164478945 - ATAAATAATAATCATAATAGTAAATAAGTGGGAATGAAGGATATAGGCAAAAGAAAAGCAAGGCTAACCCATTTTTATTAGGTTTCCAAAGAGAGAGGAAAGAAAAACGACAGGCTATTAAAGAACTTTTAAATGAGTTCCTTTCATGTTCAGTTCTCACTCTTGAGCTTTAGGAA Homo sapiens hg19 +snp_rs12636227 snp_rs12636227 1 chr3 65065315 65065552 - TATTGCACAGTTTTATATAGTATGATGATTTTCAACAATGCCCGTATCGCTTTATAGCAGAACTGACTTTATGTTGAAGCACCCTGTGGCTGGCAACAGCAGGGAGCTATTACCACTCTTAGGTCTGAAGGAGGAGAGCAGAGAAGATGTCATGGGAATCCTGAGGGGGAGAGGGGCCCTGCAGG Homo sapiens hg19 +snp_rs10038337 snp_rs10038337 1 chr5 11512269 11512495 - TTAGGAGAATTCCAGCAGCAATGTGTAGAGACGGATTATAGAGAAGCAGGACTAACCGCACAATTTATAGGATTTGAGGACTGAACCAGTCATACAATTTGCAGGGTCTAGTTCAAAATGAATATTGTGGAGCCCTTTGTTCAAAAATATTAGGAATTTTAAGATGGCAACAG Homo sapiens hg19 +snp_rs10509415 snp_rs10509415 1 chr10 82472909 82473133 - TATGGAAAACATACCTATTTTTAGGTGATATCTTGTGTATTTTTTAAGTTGTTTTACGCACATTATAGAAACCCTTCCCATTTAACACCTTAAAAAATAACTGGGTTTGCAAAATTTCCTGATGAAATGTGTATAATTAAATGCACTTGTGAACACTGTGATTACGGTA Homo sapiens hg19 +snp_rs10757399 snp_rs10757399 1 chr9 23186299 23186491 - TTTATATGACAGGCAATAGACTGAAGTATTTAGGGGATTTTAGCTGTAACGTCTTAGACTGAGGAACCATGCAAAGGTAGCAGGTTCCTCCTGAATGAAGCAAGGAGGAGCTAAAGCCAGTTACAAAGGGTGAAAGTA Homo sapiens hg19 +snp_rs10919337 snp_rs10919337 1 chr1 170216839 170217040 - ACTGTAGTTTCTACAAGAGACTGGGTGAAGCACACTTTTCAATTTTCCAACACTCTTCAAATATGTGTTCCACCCACTAGACCCAAGCTCCTCAACTTTCTTGTTCATCTCTGAATCTCCTGCTCCTTTTCCACATTTTATTCTCATA Homo sapiens hg19 +snp_rs11205541 snp_rs11205541 1 chr1 49254244 49254474 - TAAATGAATGAACAAATAAGACAGTCTTAAAGGAGTTAAGAATCTTGCCTACATTTTCACAGTTAGTGTCCCAGAAGAATTAGGACATAAGGCAGGGCATCACAGAAAAATTCATGCAAGGAGACAAAAAGAGAACCCAGAAATGGAAACAGAAAGGCATAACATAGTTCATCCTTT Homo sapiens hg19 +snp_rs10819072 snp_rs10819072 1 chr9 101361434 101361623 - ATTCCAACAAAATGTGCTAGAAGCCCACATATAAAATCTCCAGAAGGGAACCCTTCTGGTTAAATGGTGGTGGGGACTCAGAGCCTTGCCCAGTAGGGTCATGCCATGTCAGTCTTTCTTCAAGAGGCCTCCTGAGG Homo sapiens hg19 +snp_rs1078814 snp_rs1078814 1 chr3 193732876 193733071 - TCAGGGATGGAGAAAGAGAATTCAGATCAGGTGAATCCCTGAGTGGTGAGCCTCAGCCACGGCTTCATCTTGACAGACATTTGCCCTCTAGAAACAGACTTAAGGTCAATCCCTTTGCCAAGAAGTCAAGAAACTGCCTTCT Homo sapiens hg19 +snp_rs10487657 snp_rs10487657 1 chr7 82712960 82713214 - ATTAGCTCCTTTAAAAGATATATCAAGAAAATACATCGCCACTGGAGGAATTTCAAGAATCTGTTCCAATAGTTGCAAATATGTTTGAGTGGGCAGGGTCATCACTAGTACTGTCTGAAGTCATGACAGCAACCTGAATTTCTGCTTTTTCTACATGTAGACTTAGGGATATACTTTTTACAATTTTTAAAACTTATT Homo sapiens hg19 +snp_rs10930331 snp_rs10930331 1 chr2 151750485 151750677 - CAAACTAACAGCCAGGTGCTGAAATTTTTATTTGCCTTAAAATATAAATACCAGTCTTTCTTGCTGTTGCCATTTTTCAAGAAACATACTCTATGACATATCCAATTTGGGGATGCATAATTTTCACCTGCAGGTATAT Homo sapiens hg19 +snp_rs11075329 snp_rs11075329 1 chr16 17123680 17123910 - TTATTGATGACATTTGTTGAATAAATGGCTCAAAACCCGAATTTACTCCAGTTAGCACTCAGTGCTATCATTTGTGCAATGTGGTATCAAAGTGAAGTCTCCTTTAGCCTAGGTTCCAAAGTGACTGATGAGAAAACTCCAAATAGTCAGTGTTAGAAATACAGTAAGAGTAAGAAAT Homo sapiens hg19 +snp_rs10050438 snp_rs10050438 1 chr5 10138985 10139198 - GCCCACAGACGTGGAAACTGGGACACAGTGATTTAAACTCCACCTGAGGATGTGATCCAGGAGAGTGTGGAGCAAGGAGGTCTTTCTGTCTAGTTTATGGCTTCCCTCGCTGAGTGGCGCTGCCTCTGCCCTTGGCCTTGCTGAGATTTTATAGCTGGCAC Homo sapiens hg19 +snp_rs10425564 snp_rs10425564 1 chr19 57312827 57313043 - TCTGTTTCACTGAGGAGAATATTAAAAGGGACTGGACGTCTGCCCAGTTGAGGTCATGGGTCTGAAACTATTCTGAATGAGGTTTTGAAACCCCTCAGGATCTTCCCTTAGTCCTTTAGAATGAGACTTTCCGTTATAAAGCTCTGAAGTTGTGAAGGGAAAAT Homo sapiens hg19 +snp_rs11266838 snp_rs11266838 1 chr7 126792683 126792902 - ATTATTTTTATTCATGGTTTTACCTTTTGGTAAATTCCTTTGGTGATCTTTAGATGGTTTTCTCCAAGTGTCATCAGATGCATCTCCAATTTAAAGAAATAATCTCTGTATCATAATACCTACACTCTTGTATAAAGAGAGCTCAAAACAAATTGGCAAAGGAAGAG Homo sapiens hg19 +snp_rs10870311 snp_rs10870311 1 chr10 134290364 134290563 - CTGCTCCTGTGACCGCTGCAGAGTGGGTAACAGGAGGGAGTTGATAGAAGCCCTCAACCCAAGTGCCCCCAGCTGATGAGCACCCCAGCGGCATCTCTGACCCGGGCCGGGAGCCCTGGCTTTCCAAGCACATCACAAGCTAGGCCACTG Homo sapiens hg19 +snp_rs10993058 snp_rs10993058 1 chr9 96872990 96873207 - CTAAGTGTGATATACTAGAGAACATCATAGGATAATAATAGAGCTGGTTCAGCCTTTTCCAGGACAGATGTGTGATATTTTCACTAAGTTATGGACAGCACAGTGTTCTCTTAATGCCATCATAAAATTTAGTGCTAAAGGGACCTCAAGGTCCCTGAGAAGGC Homo sapiens hg19 +snp_rs10972175 snp_rs10972175 1 chr9 34625252 34625454 - CTTCCTCCAGCCATGTCTTCCCTGTTTTCCCTTGATTCAGGCAGGGGACACCTCACGTGCTCTACAGCAGGAAGGACTAGGAATAGACTGAAGGAAGGACTTCCCAAGGGGTGGGCTGGGGACTATGTGAGTTGAGGCTGTGGAGGAGGA Homo sapiens hg19 +snp_rs11582151 snp_rs11582151 1 chr1 37796448 37796646 - CAAGGCCAGCTTCATGAAGACTACCTACATCCTCCGACAGAAACATAGCTGCACACATGGAGGCCGTATTTCTGGATCAGACCCTGCTGGTTTGAGCAGACGTGACAAGAGCAAGAACCCTGGCCGAATTTTTGTTGGTGGCTCC Homo sapiens hg19 +snp_rs11085825 snp_rs11085825 1 chr19 13007286 13007515 - CGGATGCCAGAAGATGCACTGTGAGTCAAATGACTGAGCTGGTTCAGGCCCATGTGTCCCGGGCAGAGCCGGGATGAGCGAGACGGTCACCAAATGGGGGCAGTTTTCAGCACGTCAGCGAGTCCGGCTGAGTAAGAATCACCACTGTGTGGGCTCCACAGGCACAGGGAGCCGCGTCCCC Homo sapiens hg19 +snp_rs10246620 snp_rs10246620 1 chr7 43423961 43424159 - TTCTTGCTAATGTAACATCTTTTTTCCTATGGACATGCCACATGGATACTTAGGAAAAGCTCTCTAAGGTCCAAGGGTGAGCTTGCTGCCAGCCCCAGGCACACCGCCATCTTGGGGCTCTGTCTTCCTGCAGCAGCTGCCAC Homo sapiens hg19 +snp_rs11045044 snp_rs11045044 1 chr12 20257725 20257957 - AATAGAGAATGGGAAATACATTGGTTGTTTGCACATTATCCTACACTATGGTTTCAATGGTTGTCTCCTCTGAAATTTATGTTGAAGCTTAATCCCCAGCCTGGCAGTATTGAGAGGTGGGCCTTTAGGAGGTGACTGGGTCATGAGGGATGGATTAATCCATTCATAGATTAATG Homo sapiens hg19 +snp_rs10189240 snp_rs10189240 1 chr2 144484337 144484553 - ATATCTATATAGTGACCAGCCTTTGTGCTATCCAGGTTTGCCTTTTGCTATTGGCTGCAGTTAAGGCCCTTTATCAATGACAGCAAACAAAGTAGGTGGTCTTCTACTTCTTTCTTGCAGCAGGAAAAAAATAGTGACATAATTTTTCACAGCCTGAAATAAT Homo sapiens hg19 +snp_rs11008285 snp_rs11008285 1 chr10 31130832 31131040 - GAGGTATTTTGTACCATATAAAAGATTGTAAAAAGCTTGAGTAGACAGATCTTAAGTGCCGAATTCAAGGATGGAAACTACTAGGAACCACAGAAGTTGGCATTTTTGCAGGAAATGCATTTTATTTTTATTTTATATATTTTTTTCGAGTTGGAG Homo sapiens hg19 +snp_rs11139732 snp_rs11139732 1 chr9 85365353 85365570 - TATCTTTGTTATAATAATAAAGGGAACAAACATGGGTAGCCTTTTTCTCTGGCACCTTACATTTCAGACCTCAGGGGGAATATAAACATATCCATGGATTATTTTTATAATCTCAAAGGGTCAGTTTTTCATCTTCAAAGAGTCAAATAGAATGAGAAAAGTTGT Homo sapiens hg19 +snp_rs10736719 snp_rs10736719 1 chr11 61999583 61999784 - AGGTGGACTTCATCAGTGACTCAACTCTGCAGCCAACAAAGGACCCAATGTTATGCTTGCACACAGCAGGTGTGCACTAAATACAAGATAAACATATTAATATGATTGGAGTTCATTTCAGTCTGTTTTGCTGGAGTCTAGATTCTA Homo sapiens hg19 +snp_rs10891556 snp_rs10891556 1 chr11 113352608 113352823 - TCATTTATTGATTCACTCACTGGGAGGGGCAAGTACCAGCAATGAGGCTGGAAAGAGGCAAGGATGGATGTGGTGTTAGCATGATTAGAATTTATCTCAAAGGCAACAGGAAAGGCTTTGAAGGGGAGTAAGTAGGATGACATCATCAGATTTATGTTTAAGAG Homo sapiens hg19 +snp_rs10741165 snp_rs10741165 1 chr10 130610872 130611080 - AATTAGGAAGGATGTAATTATGACATTACAAAAGTTAGGCCATATCTGTTAGGAATTTACACAGTGAGCTTTGAAGCCATGGAAACTCCTAAATGAAACTTCCTGTGTTACCTGTTTCTGAGGACACTGCAAAATGTCACCAAAGCCAGAACTAA Homo sapiens hg19 +snp_rs1055273 snp_rs1055273 1 chr16 58028786 58029008 - GGGGCAGGGAGATGCCACCATGCTTCTCTGTCACCGTAAGAAGGCTGACCAGCCACGCCCACCTCCTCTGTCTGACTGAGTTCCTTCCTGTGGCCACAGGGAGGGGCTGGTCCTTCCCCTCGGTGCTGGCTCTCTGTCACAATGCCTCAAAAGACATGGAACCCAGGC Homo sapiens hg19 +snp_rs10740396 snp_rs10740396 1 chr10 74019880 74020105 - TATCTTTTTATTATCACACATGGTTATTATGGGAACTTTTCTTCAGCACTTAGTGCAGCTGATGCGTTCGATGAGGGCTGCACAATAAGGTGTGTTGCCTCCCTCGCCAGGAAGTTTTTAAGAGTGTCTGGGCCAGGAAAGAAGGTCATCAGTAGGCCTGCAGCAGCTTCCCC Homo sapiens hg19 +snp_rs10112900 snp_rs10112900 1 chr8 19646350 19646553 - ATTACATTCTCGGTATATCTGCTTTCCTATTTAAAAATTTTCTTTCTGGAACAGGATTGGAAAATAATAGAAAACAGCTCACGCAGCTGCCTTAGTTACCAAGACAACAAAATGGAGAAATAACTGGCTGGTTGGCTTTTTTCTCTTTTT Homo sapiens hg19 +snp_rs10422772 snp_rs10422772 1 chr19 9723247 9723495 - AAAAACCCTACAGTTTTCTTTTTTTGAACAATTAGAGCCAGTGGCGTAGAATTCTGGCAAAAGGGCCCATCATTCAATCTGGAAGAAATCAAGAAGTCAGGGAATAAAAACAAGGAAGAAAAATTGTAAAAATTATAATTATCAAAGTAGGCTGACATGGTAGCTCATGGCTGTAATCCCAGCACTTTGGGAGGCTG Homo sapiens hg19 +snp_rs11002468 snp_rs11002468 1 chr10 80011892 80012099 - GAGCAGCAGGACCTCCAGCCCCGGGGCAGCTGACAGTCCCCGGAGCCCCACAGAGTCCCACTGTGACCCAACCCTCGCCCCAGCCCACCTGGACAGAAGTAGTGTGGGTGCCAATCAGTTGGCAAAGCACCTCTGCTGACCTTGGCCACCCAGGG Homo sapiens hg19 +snp_rs11044070 snp_rs11044070 1 chr12 18546072 18546289 - TTTCACAGTCCAGAATAAAACTGCACCACACTGATCATTAATAATTTTATTTGAGTGGGTGAAACAGAGGAAAATGTTGCTTATTTTATGAGTGTTATTAGCTTAAATAGAAACTGAAATATAAAACAATTAGAAATCACCAGGGTTAATTTAAAAACACAAA Homo sapiens hg19 +snp_rs10139797 snp_rs10139797 1 chr14 101708446 101708648 - TCAGATGCTTCTCCCCTTGTTTCTCCCATGACTGAGCAGCCACGCATCTGGACAGGTATCCAGAACACTCCCTCCCCTCCCTTCCCCTCCCCTCTCCTCTGTCTCTCCTTCTCTCCTTCTCCCTACAGGGTGACTGTGCATGTCGGCTGCC Homo sapiens hg19 +snp_rs10825371 snp_rs10825371 1 chr10 56435198 56435416 - GACTTGTCAGAGAAGTCTTACATGAGGAACAAATTCTTAGGTCGAAATATGAAAAAGGAGAAAATGCCTAGGCAGAAATAACTAGCTAAAAATAAAGTAAAATGAAATTTGGTTATGGTAATAAATAGAGAGAGTTAAAAATTAGATCAGATTGAAAAAAAAAAAA Homo sapiens hg19 +snp_rs11017755 snp_rs11017755 1 chr10 132944018 132944222 - TTTCAGCATTTTCACAAAGGATCTTTTCCGATTAGATCTAATACATATTTTATTAGCTGCTGCGTGGGGAAAGCCCTCCTCCCAGAGCATGTGGATTCAAACGGTCTTGACTCCACTGCAGACATTTGAGAGCAGGAGCTCCCTGCCAACTTG Homo sapiens hg19 +snp_rs11134290 snp_rs11134290 1 chr5 8202376 8202573 - AAAGAAAGGAAGCATTTTCCTTTGCTGGATGGAGACTGGACCCCTAGCACAGCCCAGGGACTGCTGTCCAGGTGTACATCTCAGGGAGGCCCTGGGAGGCCTGGCTGGGCTCGGGTCCTGTGTCTCACATGAACCTGCACCATGGC Homo sapiens hg19 +snp_rs10803015 snp_rs10803015 1 chr1 242243025 242243218 - CTGCCCTTGGCATACTACCATGCTCAAGTGACAGTTTTCAGTTTCTGGAAAGGGTGAAAAACAATTACATTATTTACCAGAAATCCCAAGGAGAGGCTGGGTGTACTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCC Homo sapiens hg19 +snp_rs1038074 snp_rs1038074 1 chr5 150358789 150359005 - TTGTGGGTTGTCCACATATCGTTTTCTAAGTTTGTTCTGACTAGTTCACTTATTAATATTTTAAAAGCCTTTGTGGTCCACAGTGAACATTTATTCTCTAATAAAAATGTATTTTCTGTAATATCCTCAAGAAATATTTAGGAATCACATCTGGAATATGT Homo sapiens hg19 +snp_rs10207380 snp_rs10207380 1 chr2 241860726 241860951 - GCTTCTATTCCCACTGGCCTGTTCCCAACATCTCCCCACCCTGTGCTAGGAAGATGCCTCCCCCAAGGCCTCCCCACAGCTGTAGGGGCTCCCAGGAAGAGTAGGCTGGCTGGCAGCTCACGGATGTGCTGGGGCCCCCATCAGGTGGGGTGGACCCCAGCTCCTGCCCTCAGGGGC Homo sapiens hg19 +snp_rs10235210 snp_rs10235210 1 chr7 116003288 116003485 - TCACATGTGTCATGTGGTGGTTTGTGGAAATCAATTGTTAAGATGACTGTTAGCTAATTTTCCAGGTGAATTCCTCTTCTTGCTCTACATATGAGATAATTTTAATGTAATAGACATGTTGAGGCATAGTAGGGGGTGGTTT Homo sapiens hg19 +snp_rs10185490 snp_rs10185490 1 chr2 71166689 71166882 - GTCTCTCCCGTCAGATGTCTTAGAGCTCTGCCTCTCCCCTGTTAAGCCAGCCTGATCTTTTCTTCTAGGCTGTTTGGTTTGGACACAGCCAAAATGGGGGCTGAGCAACAGAGGTGTCCTTGACTGCAAGCCGGTCCTT Homo sapiens hg19 +snp_rs10109406 snp_rs10109406 1 chr8 72632532 72632726 - GCCAGAACACCAGTGATTTTCTGCCATAAAGTTGAAAAGTACTGTTTGGCCCAATCAATGGTGAGATGAAAGTAATATATCAATGGTAATCATGTAAATGACTTACTTGATTACATAAATTATTCAGTTAACTGAATGGAG Homo sapiens hg19 +snp_rs10095650 snp_rs10095650 1 chr8 82918215 82918451 - AGGGAAGCCACATTTCACAGTTTAAAAGTTCACATGAAAAGCAAAAGTGCAACGAAACTACCCGGAGTCTATGAGGGAACATCGCCAGATTAATAATGTGTGAAATGTAGTCAAAACCCTGCTGCCCATAGCAGGTATTTCAGCTTTTCTTAGACTGTTAAGATAATTGGAAACTTTTAAA Homo sapiens hg19 +snp_rs10840020 snp_rs10840020 1 chr11 8339720 8339943 - TCAAGTGACCCACATTTTCCAGATAGTGTAATGTGTGGCCATTGAAGCACCAACAGTTTATCACTTAACCCTTTGGATGAAAATCATCCCCAGAAGTTTCTAGATCTCCCTTTACATAAAAAAAAACCTATACCTTTATTTCTTTTTATTAAAATAATAAATATGCATTAT Homo sapiens hg19 +snp_rs10502584 snp_rs10502584 1 chr18 29797319 29797530 - GTATCTCCAAGTTAGGAAAGGCCGATAGCACAGATAACAGAGAAAGTTTAGTTCTCAGTGTCCCATGCCCGCCACCCTCCAGATTCACATCTTGGCCAAGGGCTCCTCAGAACGTCAGTATCTTCATCTAGAAAATGGAGGCAGCTACACTTAAAA Homo sapiens hg19 +snp_rs10106093 snp_rs10106093 1 chr8 29355272 29355473 - TTTATGTTAAGTTGTTGCTGTTGCGTACAAACAAGAAATTCCTTCCCTAGCAGAGAAACATATTGCCACCCCTTCAAAAGATCAGAATGACTCTAACATGAGACACATCTTGCCAGGGCTGCTGGGGACTCACAGGGCAGGAAGAACAGG Homo sapiens hg19 +snp_rs10832136 snp_rs10832136 1 chr11 13925578 13925779 - TCAATAGTAGTACACGAGTGGCAAAACCTAAAGTCTGAAACCTGTACTATTTTATAATTATCTATCATCGGAGCTCATAATGCCCTGTGAAGGGATTTTGTTGGTATTTTAAAATTTCTTTACAATTAGACCTGACTGGCTCATTGG Homo sapiens hg19 +snp_rs1028530 snp_rs1028530 1 chr14 27441005 27441195 - TGGACTATAGGTCGGTAGTGGAAGTCAATTTCCAAATATTCACAGCTTCTCAGTGTTGCACCCAAGTTTTAAACAGTAGTGTTTAATCCAGCTTGAAGTCTGCAGTTACCAGAGAAGTACCTGAGCTTCTCCCACGTT Homo sapiens hg19 +snp_rs10936922 snp_rs10936922 1 chr3 176675123 176675357 - AAAAAAAGAAAAAAAGAAGAGAGAGGACGGGTCATGAGCAGGTGCATCCTGGGATGCCTCATTACTTTAGGAAAGGCCCTTATAGGCAGAGCTGAGAACAGGAAGAGAGGCCAGACCAGAGAGAGCTGAGATGTGTGGTGGGTGGTGGGCCTGGCTCTTTATGAACAACTCTTTGCTGAAA Homo sapiens hg19 +snp_rs10184938 snp_rs10184938 1 chr2 9912848 9913056 - AATGTCCATAAGTTGGGGGTCTACGGTGTGTCCGGTCTGGGGACAGAGATGGGACCCCCCAGAGACACCGAATGCAGGATTCTTTCGACATCTCCAAGAGGTGCTGCTGTAAGACCCCCGTGTGCCCGGGAGGAAAGAGAAGCTGGTGGACTTGGGG Homo sapiens hg19 +snp_rs1028850 snp_rs1028850 1 chr13 40941330 40941524 - TTAAGAGATGGGTTTGCAATAGAAAGCCCAGGATTGAAATTCACAAATTATTTACAAATGCTTTGAAATTACAGTGCCTATAACTTAACTTCTGTGTACATAAAAGTCACCTGGAGGACTTGCAAAAAGATGCTTGAACCT Homo sapiens hg19 +snp_rs10913469 snp_rs10913469 1 chr1 177913365 177913568 - TTTATGTCCCCTAAAGGTCTGTATTTTATAATATGAAGGCAAAACCTTGCAGAGGCCTCTCTGCTGGAGGCTCCTGCCTCACTGCTGATGTTTGAACGTCCTGCCTGCCGCCCCGGCCTGTGCCTCACTCCTGCTGTCAGCTCCTTCTCCCC Homo sapiens hg19 +snp_rs10490198 snp_rs10490198 1 chr2 67121519 67121740 - TTCAAAGAACATAGCAAAGGCTTTCAGCAATATGTAACGGTGGAATGAAAAAAGGAGCACATCTGACAATTCTAGAATTCTTATTGTCTCTCATACTAGTTCACTGATGCTCAACCACAGTCTATGTTGTCTCCCAAGGGACAATTTGGCAATGTTATAAGACATTTT Homo sapiens hg19 +snp_rs1147960 snp_rs1147960 1 chr10 44971311 44971532 - TCATCCAACATTCATCGAGCACCTATGGCATACTGTGCCAAGCATGGGTTGTCCAAAAGTAACTGATGCACTTCCTTTACATGAATGTGATTAAACACTATGTAACAACTAAAAGAGATGCAGAACGAACATTTAATGATTTGGAGAAGGAATATATTCTATAGGAAAAA Homo sapiens hg19 +snp_rs10489168 snp_rs10489168 1 chr1 44727828 44728042 - AATTGAATTCTCCTGCGAGAGCTCAGATGGGCATCCAGAAGGGGGCCTTGAACTGGGCCTCTGTGAAGGATGGGGACTGTGCTGTGGAGACAAGTGTAGGCTAGCATGGGGCAGAGAGGACAAGTGTCAGAGATCAGTTGGTTAGGGTGGGGCTGGGCCCAG Homo sapiens hg19 +snp_rs11241298 snp_rs11241298 1 chr5 114282888 114283088 - TATTTCTTGCTACGAAGCATCTGGGCACAGGAAGAGTCTATTTAACCTCCTGAAGTGGACTGGGGAATGAGTCTGGTCTAAACGGATGTTCTTTGTTGGCTTCTGTTGACCTCAGCTTTTCTTGCCTGGTTTCTGGGAATTGACTTCT Homo sapiens hg19 +snp_rs10935172 snp_rs10935172 1 chr3 135275536 135275741 - CTTCAGGGCCTTTGGGTGTGATTCATTGGCTTCTGGACATCTGAACTTATATGATGGAGGTCAGTGCTATCTGAGCATGTCTTTCTCTGCTTGTGACTTTGGGGCATTCTTGACCATTAAGCATATGCTCTGGGGCCGGGGCAGACCAGGCCTGC Homo sapiens hg19 +snp_rs10746385 snp_rs10746385 1 chr1 219706253 219706467 - CACCTTCTATGCATAAAAACCCATAGACCACAGGTCAGATTTCTTGAATGTGTTGTGTGAAGGCATGTGTGTGCTTTAGGATTTTATTATTTTAAACTTCTACTTAATTATAATGTCATATATTATTCTTTAAGCTTTATATTGCAGCTAATTTTAAAAAT Homo sapiens hg19 +snp_rs10834253 snp_rs10834253 1 chr11 24001808 24002038 - TCACTCACACCCCCTCTCTCTTAACCCCTTCTTAACCGTTTCCAAGTAGGCTTCTCTTGAGAAGGGGTCATTTTTGGTGTTACTTATGGTCTCAAGATGGCCACATTTGGTTGCAGAGTTAAATAGGGCAAGAATTCTTGTTCTTGAAAATACCTCCTGTTCAATGAGAATATAATT Homo sapiens hg19 +snp_rs10068395 snp_rs10068395 1 chr5 178252212 178252426 - CTCCCTGGCCTCTGTTGGACAATCTGATGAGATGGAGGATGAAGAAGGCTGAGCCTTGTGTCCTACAAAGATCCTGAGAGCCAGAATCACAGGTGGGTCAGCTCAGTGGGAAGGAGAAGGGATTCTGGAAGCCAGTCCTTCATGGGATGCTCTCCAATAA Homo sapiens hg19 +snp_rs10482536 snp_rs10482536 1 chrX 123884032 123884243 - GTTATAAAAAGTCTCTAATTTGATTCTGTCTTCCCCCCAGAAATGATTAGCCACTCGTTTTAATGGAATACCCACAGCCATAGTCTTCATGACAACAAGACTCTGTGTAAATGGTTTCAGTTGGAAGGTGGGAAGAGGCCTTAACATCTGTGTAGCCT Homo sapiens hg19 +snp_rs10512096 snp_rs10512096 1 chr9 82730172 82730406 - CTATAAAATAGTCAATAAATAGGCAACAGATAAATTAACAGATAAAGGCATGACTTTCTTTCCAGATGAACACATTCTTTAAAAGGTGCCAAGACATGAGCAAAGAGAAAAATTTTGTTTCCAGGCACAGAGTGGCATCTGACATGTAAATGATACAGACAACAAGTGCTACAGCAATTT Homo sapiens hg19 +snp_rs10765017 snp_rs10765017 1 chr10 129168728 129168937 - GGCTATTGGCACCTATTTGAAAGATCATGGAGAGAAGGATCCCAGTAGTAGCTAATCCAAAAGCCAATTATATTTGGTTTGGAACGCATAATTTTTGTTTTGGGTGAGATTTACTATTCTTACTCTAATGCATCTATAATTTTATACATCTGTAAT Homo sapiens hg19 +snp_rs1049564 snp_rs1049564 1 chr14 20940455 20940646 - TTGGGGATTTCACCGTAGTCAAAGATCTGGGCCTGAGTTAATTTATCAGTCAGACCTCCTAATCCAGAACCACAGATTATTGCAACTTGAGGTCGGTGCTTAGTGTGAGACAGAAGCCATTCTGCAGTGTTCTTATAA Homo sapiens hg19 +snp_rs11094448 snp_rs11094448 1 chrX 147217241 147217437 - TGATGTTTGGAGGACTGTATGTCATGTTCTGCTTCCAAACCATCTACTTTACTATTGTTGTGAAATACAGATCTCTCAGACAGGAAAAAAAAAAATTGATTTGACTCAAGTTTTGCCTACTGTTTCTGATGCCCAGGAGTTTT Homo sapiens hg19 +snp_rs10852042 snp_rs10852042 1 chr15 96562980 96563173 - TATATAAAGTAGATGGTGTAGTCGGGTGTGACTTTTAAGATTACAATGAGTTCTGAACAGGTCAGAAGGATGGTAGCAGGTAACAATTGGAATTTGCACTGAGGCACATGCTTGCCTGCAGTACTACCGTGAATATGTAT Homo sapiens hg19 +snp_rs10492367 snp_rs10492367 1 chr12 28014811 28015013 - TACTTATTATTAGACCCAGAGTGCTAGAGAGAAAGTGTGACAACCAACAGCTGTCCACAGCTGGCCTTTGAAAAACAGCTTCTTGAAATTAAATGCAGCAGCTGCAAGCGCCTGGCCAGCAGCATTCTGGGAAGTCACCTGTGTCAAGG Homo sapiens hg19 +snp_rs10519420 snp_rs10519420 1 chr4 138313010 138313220 - TTCTACTTCCGTTTTTACTGATTATACATCTAACTAAGCTTCAGTGAGGTCATAATTAAATGTAATGTTGTTTTTGGTTTAAAGGGAAATCTGCAATCACAGTAATGTGTGTTCATGGAACCTGAGTGTTATCACATGAACACAGACACCTGACCCA Homo sapiens hg19 +snp_rs10278557 snp_rs10278557 1 chr7 15698880 15699077 - CACATAGCAGACACAGATATAAAATTTTCATTTTATATGCACACACCCGACTGCAAAAGCATTTGTTTTTTTACTACCACTAATTCCTGTGCTTACATATAAATATATGAAAATTGGTTGCAAAAAAGATGCAACATTAT Homo sapiens hg19 +snp_rs11017144 snp_rs11017144 1 chr10 132012809 132013003 - CACTCCCTCTTGCACTCATAAAGCATGGCTCCCAAGGTGCACAGCACACCACCTTCAGGCCCCGGAGCACGCTCTGAAGGCAGCAGAGGCAGCGGCAGCAGGCCTGTATCTTAGGATTCACCAAGTACAACTCCCCCTGG Homo sapiens hg19 +snp_rs12651141 snp_rs12651141 1 chr4 89287556 89287747 - TCTAAGAGGAGGCAGGAGCGCTGCAAGTCTCCATTGTTCTTTTGCCTTTCTCTTCTTAGACTGTCTTCTCTTTAACTCCATTGTTCTGAGTTCAAAGCCCACACTCCGTGCTTTCAGCCCTTAAGACAAATAAAAAAAT Homo sapiens hg19 +snp_rs1040247 snp_rs1040247 1 chr8 139533211 139533407 - AGTGTGAACTGTATCATGCCCCAGAGCAATCACCTTCTTAATAATAACTAGCATTTATAATGCAATTGCAACATACAGAGTGCTTCTGTAACTCTCATGATTCTCCCAACTGTGCTGTGTGGAAGGACTTGTCAAGGGTTACACA Homo sapiens hg19 +snp_rs10103493 snp_rs10103493 1 chr8 97352386 97352583 - GTGTTGAGTGAATAGGTGTTTGTGAGATTATGTGTTTCTGTGGGTGGATATGTTTGCGATTTCAGGCATCCTATTCTCATGCACACTCCTCCACCGTCAGCATACTTAACGGACCACACCAAGAAAAACACAGCTCCGTTCACT Homo sapiens hg19 +snp_rs10180924 snp_rs10180924 1 chr2 86021761 86021963 - GGGCAGGGGCAGTTGTTCGGACAGCGTGTCCAGCTCCTTGTAGGAACAGGACCTGTGAGGCTGCCAAAAGGGGCCAGGGCCTCCCGGGCAACTGCTCCCCTCAAACCTGGCTCCTGTCCAGCCCTGTTCTCAAAACCAGGGAAGGCAGCCC Homo sapiens hg19 +snp_rs10061008 snp_rs10061008 1 chr5 141744359 141744551 - TGAAGGGCAAAGTCGAAATGCAAAAACACCGTAATTAACGTTTTGTTTAGAGGCGCTTTCAGAGATTTTGAACCTTAGTCTCAGAACCATTAGACACCCTTCAGCAAACCACAGGGCTGTCCACCAGGGTGTCAGCCCCA Homo sapiens hg19 +snp_rs12570664 snp_rs12570664 1 chr10 1816144 1816340 - CACTGCCCTGTTGTGTCCTCACTCATCCGGGAAGGAGGGAGAGGCATGAGCCAGGCCAGTTACAGCATAGAATAAAGCCCAGCTGCAGCCATACCTGCGGTCGGAATTACTTCCTCACAGACCATTAGCAGAGGTGAATATATA Homo sapiens hg19 +snp_rs11017185 snp_rs11017185 1 chr10 132096004 132096235 - TGTTGATGTAGTTGTTTCTTTTTGGGGAGGGAAGTCATTTTCCAGCTAATTTGTATAGAGTTTTGGACACAAGAATCTAGGACCAAGCCACACCAGTTCTCTCCTTAATCCACTACATTTACCTTCTGTCTTAGCCATGTTTCCAGAGTCTGTCTTGCCGAGACCAGCTCGGTCAGGGAGAC Homo sapiens hg19 +snp_rs10252308 snp_rs10252308 1 chr7 148501551 148501740 - ATACATACTCAGCCTGTGCATCTGGTCTTAGTGCACAGCCCAGCTCTGATTAAACCACAATGAATTTTTCTACAACCCAGGAGGTAAAATATTGATTTTATAAAATATGAGTTCAAGTTGTCAATAGATTAAACCTTT Homo sapiens hg19 +snp_rs10490542 snp_rs10490542 1 chr2 207587156 207587383 - ATTTTATTATGGGACATTCTAGAGTGAATCTGTGCCCACTTACCAGAATTGTTTTAAGTGTATCTTTTGGGACCTGAAAACTCAGATATTTCAGCTCTCCAGGTGTGCTCATGAAGTAAAACACCTATGCTTGGAGTTCAAACATTTTTTAAAGACATGTTAAATTGATTCCTATA Homo sapiens hg19 +snp_rs10776798 snp_rs10776798 1 chr1 115862094 115862292 - ATGTATGATTTTGTCAAGTTTTAAAAACAACTGATGCTACCACCCTTGTACCCGCACTACCATTCCACTTCTCCAAAGAAATTTGCCAAAAGAAAAGGTGAGTTTTGAGTTCTACTAAGTCTGTTAGGAAGCAAGGATGAGCAGCC Homo sapiens hg19 +snp_rs10894631 snp_rs10894631 1 chr11 132829527 132829716 - GTGTGTCCTGAAGTATTCTCTCTTTCCAATTTCCTTTCTGCCTTCCAGATTTAAGGTGCCACTTCTAAATCTGAGCCTGTGTATAGTAGTATTGTATTGTGTGTAGATCCTGATATTTTCCCGAAGTCAATGTAGGTAA Homo sapiens hg19 +snp_rs10505173 snp_rs10505173 1 chr8 113486062 113486272 - CTTCAAAGGAAATCAAACGATCAGCTTTAATACTGATGAAATATGAGTGGCAGTGACAACAGGCTTCCTACTAGCTGTCGGCAACAGGCTCAGCCCTACCCTCAGAAGGCGCCCTAAAAAACCTACAGTGTAGAAGAGCACACCAGACAGTGTGCTCT Homo sapiens hg19 +snp_rs10016530 snp_rs10016530 1 chr4 183824807 183825039 - CTGAAGAAGATGCTTGACTGGTAGGTTGTGGACAGTGTGTGAGGACATGGTAGGGAGGAAGCAGAGAAGACAGGCAGAACCAGGGGTCTCCAAGACCCCTGAGTGCATTGTTGCAGGAGCGGAGACGGAAGTTCTTGCCTCAGCTTTCAGGGCCCTGGGCTGTGGGCAGGCGGATGGGCACCC Homo sapiens hg19 +snp_rs11125183 snp_rs11125183 1 chr2 49013496 49013698 - GTCTTAGCAGGTGACTAAATGGCAGAATGGCAAAAAATTAGACAATATACTTCTTCCAAGAGCCCTCATGACCTGCCAGGACCTGCCATGTCTTGTATAAGTTGATATTAAGTGCTTAATTTCAGTATAACTATAAGCTAACAAAGAAT Homo sapiens hg19 +snp_rs10113311 snp_rs10113311 1 chr8 61888301 61888507 - GTGGCTTGTGGTATCTCCATCTTATGGTCCTCCTTGACCATTTAACTTTCACATCATTTAAGTTCTGCTGGGACATGGGTTCTTTACTCCAGCACAACTAGCTCCCTCTTAAGAACAATAATTATTTCTTAAATATTATAATTAATGTGAAAGAGG Homo sapiens hg19 +snp_rs10516939 snp_rs10516939 1 chr4 94574549 94574740 - TGCAAGTTAAGAGGGTTTGTGAATGTTGTGTTGGCAATTTTCACACATACAAAATAGCACACTTCTGGGAAGTGTTTAAATATAGGTATTATAGAATGTGCCTCAATCCATGTTCTTCTTAGAAGTGTGAATTAATTTA Homo sapiens hg19 +snp_rs10790866 snp_rs10790866 1 chr11 127063081 127063299 - CAAAGCAGAAATGAGTCAAATTAAGGAAATACGCAAGCATTCCAGAGCACAGCTATAACCATTATGCCTAACCTCCCTATCACACATTACAAATCTACTAAGTGCTGTCAATTAAAAAGGGTGTAGACTTTGGATATTGGGCATAAATAACAGGATGATAAGAA Homo sapiens hg19 +snp_rs1029864 snp_rs1029864 1 chr2 107784235 107784444 - TCTACCTCTATCTATCTGCCTTCCAAGGACACAAAGGAGCCACTCTGGAAGAAGAGAATATCATCCAGAGCCTCTGCAACTTATACAAATGGTCTAGCATTTAAGAAAATTGTCTTTGCGTGCTAAGAAACATGACAAGGAGATTAAAAAAAAA Homo sapiens hg19 +snp_rs10869715 snp_rs10869715 1 chr9 78780323 78780526 - CCCTGCAAGTGGTTTCCAAATAAATTACTTTGGATGAAGCCTGGTAGAAAAGATGACCATCAAGTGTAGTATATCCTTTTGAGGAATTAACTCAGGAAATAACTTACATAATTACTGTAAGCTTTATTTCCCTTCCTCTTAAAGAGTCTA Homo sapiens hg19 +snp_rs10248924 snp_rs10248924 1 chr7 138831555 138831769 - TACTTCATTTCTCCTGCAAAGAAACAATGGAAATAGCCTCTGGAGGCATAGCTTGACAACGACAATGGAAAGCCCTTAGGTTACAGTTAATACTATTTGACCCTTCCCCTTATCTTTTCTTTTTCTTTATATTTTCTCCCTTTCCTTTTCTTTTTCTGT Homo sapiens hg19 +snp_rs10836419 snp_rs10836419 1 chr11 35580524 35580766 - TACTGTTCTATTTGAATGATAAATGAAAGGGCCACACCATGCCGCTAAGGCTGGGAGACTTGGTGATACCAGACAACAGATATTTGATGAGAATTGAAGAATTGCCCTGATTCTTTATTTCATTATACTAACATAGATATAACCAGGGTTGAGCTTTCAAATAACAGATCTCTAGGTTTCTATATTCTT Homo sapiens hg19 +snp_rs10484150 snp_rs10484150 1 chr14 83637774 83637991 - CACTGTCATATTAACTTTACCATTGCCCAGTTTTGACAGATTCCAAAAGTACTTCATTCTTTCCTTCTTCCCTGCTGAATCTGCCATTTGAAGCTTTTCACTACAAAGACTTAATTTATTGTTCCTGTCTTATCTCTATTCTCCCCTTTGCAACTTCCTATTCT Homo sapiens hg19 +snp_rs12719046 snp_rs12719046 1 chr7 51334321 51334542 - AAAAATGTTAGGTTTCTTGGTCTAGGTGTCCATAGCACTCAAAAAACATGTGGAAAAAAACTGTGTGTGGGTGCTTGTGTCGTAGAGTCCTTTCCTTCCGTCCATTTGTGGGAAACAGGGACAGCCCTTGCATATGCCATGTTATTTGTGTAGAAGTACTTGCAAGCAG Homo sapiens hg19 +snp_rs1152562 snp_rs1152562 1 chr14 56878975 56879187 - CCAAGACAGCTCGGTTCTAGTGCCTGTTCCTCTTCATGCAGCTATTGATTTACATTTTATTTTGTTATTTTTGAAGACTTCAGCAAAATTAGCAATTGAGGTGGTGAAGTATTTTTCTCCTTTGAAGCATAACTCCTCCTTTTCTTCTATACTGAAAAAAA Homo sapiens hg19 +snp_rs12679346 snp_rs12679346 1 chr8 34068300 34068513 - ACAGATTATACTTAACCTTCACCTGGACGAGGAATGGGTCCATGACCCCTAGAATCTTCTCATGCCATGGTGGACATAACTCCTTCTCAATAATATATAAATTTGAAGGACTGAATTACCACTTTGATGACTTTAAAGAATGACTGTGACTTTCTAAATT Homo sapiens hg19 +snp_rs11095604 snp_rs11095604 1 chrX 13143740 13143939 - ATGTCTACCACGGATGGAAATTTGAAGGGCAAAACAGAAGTGATTGGAGTTCTGAGCTACAGTTGCTTATAAGCAAAAAAGCACATGTCTGTATTTTAAGATGACTGTGTTTCTCTTCCAATCAACTTTCTTCAAAGCATTAATCAC Homo sapiens hg19 +snp_rs10059981 snp_rs10059981 1 chr5 3619368 3619557 - GCCTTGGAGACATAAACTTGGCTTAACGTGGAACATTCCTTCTCTGATAGGGACACTCAACTCTGGAGTGCACTGATACCTGGAAGCCTCACAGTGAAGCAGCAAGGACATTCCTGAGACTGAGAAGCCCTCACTGC Homo sapiens hg19 +snp_rs11070073 snp_rs11070073 1 chr13 94692771 94692967 - TCTGGCCACATGCTGCAACCTGAAATCATCGTTCTCAGGCTTGACCTTTCCTCTCACTTTGTTCTGGCAGCTTTCCAAAGAGGGATAGGTGGTTTTAGGGCATTTTCTTGTGTTACAAATCAAATAATATTTCATGGCTTTCA Homo sapiens hg19 +snp_rs1144171 snp_rs1144171 1 chr6 91698101 91698320 - GAAAGAGACGCAGTGCTTGTCAAACCACGTGATCCCAATATGATTGTCAGCAGTGGAATTAAACTCCCCTCAAAACAAAAACAAAAAAACACTGAACTTGAAACCAGTTAAATTAGGTTATTTAAGTTATTTTAAAGTTTTTAAAAATTATTCTTGTGAAAATGAT Homo sapiens hg19 +snp_rs1049269 snp_rs1049269 1 chr10 73819850 73820055 - CCGAAGCCCCCACACTGCCTTTCGCCCTACTGAGACTGGTCCCCTCAAAAGGTAGACAAAACAGCAGCTCCCTGTGGAGCTGAAGGGCGGCCTCAAAGTGGCTTTTTGTTAGACAAGGTTAAGGTTTCCTCATGAGCAAGGTTGCAGATCGG Homo sapiens hg19 +snp_rs10263803 snp_rs10263803 1 chr7 20437670 20437862 - TACCAAAATAGGTCCTCTTACTGGGCAGAAAACCATTCATTCATTTATTCACCCATGTATACACTCATTCAATAAATATCTATTTAATGCCTATTGTGTGGCAGGCACACACTAATTTCTTTCATTACAATCTTCAAAT Homo sapiens hg19 +snp_rs11121704 snp_rs11121704 1 chr1 11293794 11294006 - AATGCTTCAGGCACATCATCGCAGATGTTTGGAAAGGAGAAGTAGGTAGATAGTAGCATAAAATAGCTCGCCCAAAATGAGGAAAAAATGAGCTTGAAAATCTGAAACAACCTTCAAATCTCAACACATTAGAGTCACGTGAAGTCCTTTATAATGTAT Homo sapiens hg19 +snp_rs10471977 snp_rs10471977 1 chr5 55750233 55750422 - CCCCGTGGCCCTATGTTTACCATGCATTCGATTCTCGGTGTGGTCCGGGCCTTTCTCACCTCATCCATTTCACCTACCAAGAAAGGAAATGACATTCATCCGGGCTGGGGCACTATTGCGCAACAAAACAAGCCAA Homo sapiens hg19 +snp_rs1005790 snp_rs1005790 1 chr5 160174797 160174990 - CCTGGGAGCCATCAGTCTGGCTAAGGGTCTATGGTGGACTTGAGGCAAACAGGGAGAAGGATGACAGAAATGTGCCAGAAGATGAATTAGAAGAGAAAGCAAAGGGAGGACAAAGATAAAAGCAAGCTATGAGAACAAAAA Homo sapiens hg19 +snp_rs10863725 snp_rs10863725 1 chr1 208950647 208950908 - ACTTATTCATTTATCAAATGTAAATACTAAATGTTTGGTGTATATCAGACCCCAGCTGTAGGATTGAGGATAGAATAAAGAACAAAAGAGAGAAAAGGTCTTTTTCCTCTTGGGGATTATATTTCACTAAAGGAGAGTGTATTAGTATGCCATGGTGGCTGTAACAAATTACAACAAATTAGTGGCTTAAAACAACAATTTGTTCTCTC Homo sapiens hg19 +snp_rs10930259 snp_rs10930259 1 chr2 167842485 167842681 - AAATGTATGAAGTGGCGCCCTTATTTCCAAACCTCCTCTGTCAGAGGTAGAGAATACCAATGCAGCTAGGCGGTCTTGCAAAGCACGGTACTCTCTCTGGTACAACCTGGTGCAACCATTTCCTTCTGCTGTTATAGGAAATAT Homo sapiens hg19 +snp_rs10813743 snp_rs10813743 1 chr9 32109898 32110112 - TCCCAGTGCTTGCATTGGAATGGATCCTCCATTTTCCTGGTTCCATATTGCAGATTTTCAGTTTCTCTATTTTAGCATCTGACTCAACCTACTCTACACTCTGCGTCTGTGTGAAGGAAGTTGCATTTTGAAGGGAGGACAGAGTGGCTGTTATTTTAA Homo sapiens hg19 +snp_rs10906498 snp_rs10906498 1 chr10 13859244 13859448 - TCATTCTAGTTAGTCGTGTCCTGCCTGGAAGAAGCAGGCCAGGAAGTAGTCAGGACCTGATCTGGAACCCTGTAATATGCTGGGAACGTGAACAGTTCCCACTGGAATCATCCAGTGTTCTCAAGAACTCAGATCTGGGTCCTGGAGCCAC Homo sapiens hg19 +snp_rs10195834 snp_rs10195834 1 chr2 66826907 66827099 - AATATATCAAGATATGCCCACAGGAAGCTAGGCATATATTTGGAAGCTGTAATTAGAATTACTTGGTTATATATAAGAGAAAAAAGCAAGCTAACAGTGGCAAACAGAAATAAAGAGAGAGGGAGGAAGGAAGGGGAGAGAGGA Homo sapiens hg19 +snp_rs10248887 snp_rs10248887 1 chr7 23711617 23711804 - TAAAAGAAGATGAACTTTGTGTCTATGGCCACAGTAGAAGTCTCAAACTGGTCCATCCGTGAGTTATTGGATGCCACTGATCTCTGGCCTTCTGAACCAGCTCCCTGGAACAGGAGGGTCTTTACTAAATAAGAG Homo sapiens hg19 +snp_rs10135821 snp_rs10135821 1 chr14 97199737 97199936 - GCTACATTACCTTTGATTACCTTCTGGGCCTGTGCTTTCTAATGCATGGCCTTAATATCTTGGTGGGCGCCATTCCTGTTTGGCTGAGAGACTCGGTCCCCAGCCGTCTTGGCCGGATGCCTCGGGCTGTGATGCCTGGTGGGAAG Homo sapiens hg19 +snp_rs10999042 snp_rs10999042 1 chr10 71707263 71707451 - AAAATGATCACGTAGGGGCCCACAATCAGGGCAACCTAGAAAGAGCTGGACACATGGATCTTGTTGCTGGATAGCAATGCTAAGCTGGTGGCTGCCATGGGATTCAGTCTCTCCTTGCTGTGTGGAAAAATACAGGC Homo sapiens hg19 +snp_rs10036347 snp_rs10036347 1 chr5 56694491 56694710 - TTCCTCCACATTATAAACTAAATGCCAAGTCGTGACAATACATTTCCTAATGGGAAAATAGAGACTTCACAGGCGCTAGAAAAGAACGAAGGACATGAGCTGTCTTTAAAAAGAGCAAATTGACTAATGGCTTAATAAATAGGCTTTCTCTACTGAGTGAAGCAAA Homo sapiens hg19 +snp_rs10189159 snp_rs10189159 1 chr2 50714405 50714615 - GGAACCACATTAGGTCAATCAGCGTCCCCCATTGACATCACATGAATGTGGTTTTCTGTGTCCATTCTTAAAAGTGGCCCCTTTTTGGCCTTTGCAATTAATTATTTTGGTTGTTCGTAAGGACAATACAAGAAGCATATAGCATTATAATTAATAAT Homo sapiens hg19 +snp_rs10491907 snp_rs10491907 1 chr9 9963788 9964001 - ATGAAAGAAATGCTCATAAAAATGGAAATGAGGCATAATTTTCCATGGAGCAAGTAGAATCATTTGTAAATAAGAACTTCACTTGGACTTAAAACGTTTGTGAATCCAAGTGTTTAGTTTCCAATGTTGATGAATCCTTTGACAGCTTTCTAATTAT Homo sapiens hg19 +snp_rs10737814 snp_rs10737814 1 chr1 237469150 237469346 - TCTGTAGGCTATGTTCAGAGTTTGCAGACTGAGTCCAAACCAACATCTTCTAGGCCCTCATAGTTTTATTGAAATACCTTTGTATCATATATTCCAAAATATGTATGTAAAGAAATGCATATTTTAAATAAAATTAACACC Homo sapiens hg19 +snp_rs10503087 snp_rs10503087 1 chr18 61476290 61476515 - TTTATTTCCCTGCTATGCCTGTGGAAATTGTGACCACTCCTTCTAGCCTAAGACTAAGACTCTTAGTCACACTGAAGAGTATTGTCTGAAGAGGCACAACCATGGGGTGGGAGAATGGTATAATGTAAAATAGATTGTTTTTAAAATATCTAGAAAGAATTTCTGCTCCATCC Homo sapiens hg19 +snp_rs10094564 snp_rs10094564 1 chr8 673385 673622 - GAATTTGGTATTTTCTCTAAACTGATGAAATAATGTGGTTTGTGTGTGTTTTGTGGTTTTAGTGGAAATGTTTTGAGAGATTTCTCTAATATGACAGGTGAAGGAGGCAGGGAGCAAGCACCTCCAAGCTGGCCATGGTGGAAATTTCTACTAATGATTATTTCTTGTTTGAAAATCTAATCA Homo sapiens hg19 +snp_rs11662907 snp_rs11662907 1 chr18 21455409 21455598 - TGGAGTCACTTTATTGCCACTCACTAGGCCATGGGCAACAGAGAAGCCAGGGGAGGGGAGCGTGCATGAGGTTCCCATACAGGACTGTTCACGAACATCTGGTCCACCCGAACACACAGAGGCTCAGCCTGAGGGAC Homo sapiens hg19 +snp_rs10093381 snp_rs10093381 1 chr8 87628221 87628447 - TCATATTTAGATTGGTTCAAATGTTTTTCTCTGAGAAAATCCAAGCCGTCAGCTGAAAGCTATCGATGTAAGTGCTTGTGTGTATTCCTGCCAAGAAAAGTGCTAATTGTTTGCTTATCTATGTTCAGGCTTGTCTCCTAGGTTGGTCTCACGTTTCCCATTGATCCGAC Homo sapiens hg19 +snp_rs10741808 snp_rs10741808 1 chr11 20020732 20020928 - ATAATAGACTGGGTTAAACCAGTCAGTCTCCCACAAGAGAAGTTCCTGAACATGAATAACCCGATTTTTTTGAAGGCAAGTTGGGCCATGGTTATCTCTCTTTGAGGACTGGCTGAGGACTGAGTGGGTGGGTTCACTGTGTGCCAC Homo sapiens hg19 +snp_rs11563212 snp_rs11563212 1 chr2 234869205 234869433 - AACAGAGACAGTACTAACAATACTATAAAAATATGGTAAGGAAAGCACTAGGCATTTTTCTTCCTCAGTAGCACTGTATTTCCAGCCACAGAGTAATAATATCTTCAACTTCTCTTTCAATCCTGTCTTGAGAATGAAGTTTATCTTTTTTCCGTTTTAACACAACAGAGGATTA Homo sapiens hg19 +snp_rs10514496 snp_rs10514496 1 chr16 80456253 80456446 - AGAGTGGCCGGAATAGCAGTAACCATCATGAGCTGGGAGACTGGACAGATGCCACATGACTCTGTGCACAGAAATGTTCTGAGAAACAGCCTGATCCAGAAAAGAGTGGTTTGAGACTGGCTTTTCAGAGACATTGGCAGT Homo sapiens hg19 +snp_rs11633318 snp_rs11633318 1 chr15 77602545 77602763 - AGCAGTTTACTTTGTTCAGAAAAGTTCTAAGTAATTTAAGTTCTGCTTAAACAGTGCTATGACCAAGCTAGGAACATAAGAGACTTGTAAAAGGAGTGACTCAGGGACCCCAGACTTAAACCTATTAGTTCAAACTTTTGTATGACTTCATGAACTCCTGAAAAA Homo sapiens hg19 +snp_rs10509550 snp_rs10509550 1 chr10 90219136 90219343 - TGATTAGCAAGCTCCCTGGATACATGGACTGTTTTAGTAGCGGAGGTACACTCAACCTTTCTGCAATGGTACAATACGAAACAGACAAAAAGAGCAAACTGCTTTGTATAGGCTTAGCATTAATGAATTTACTCTCTTTCTCAGCCCCAGTATTT Homo sapiens hg19 +snp_rs10758 snp_rs10758 1 chr2 113409836 113410058 - ACATCCTGAATAAAGATTGCAATACCCACATTCTAAGGTACCCAAAAGCCCTAATATAAACTTCAGCACACACCTGAGGATAGGCTATACTCTACGTTTGTAAGAGATGTCAAGAAATAGACTATGTTAGGATGTTGCTTACCTGACTTCATATCTTCAAAGACTAAAA Homo sapiens hg19 +snp_rs10281519 snp_rs10281519 1 chr7 90909877 90910063 - TTACCTGGATTAACTGATGCGAACAACAATGGTGCTTTGAAGCTCTTGGGTACAACAGTGGAAATGATCACATTTCTTGATTAATGAATGAATTCTTTCATAAGGATTTGTTTATGGAAATAAATAGAGTAATACCT Homo sapiens hg19 +snp_rs10860784 snp_rs10860784 1 chr12 102172883 102173072 - TTCCTGATTTTATAAAGAAATGTTCTTTGAGTTCTGCCACTGGGTTTAGCTTACCTGATTCTTACTTCCTCCTGTTGTATGTCATTTAACAATTTTGAGGGTGAAAGGATGAAGATGGAGTAGTGGTGGGGGAGCT Homo sapiens hg19 +snp_rs11077405 snp_rs11077405 1 chr17 76969721 76969928 - AAACTACTATATTTGTGGCGAAGAAAAACCTATGGGATTTCATTTTGAGTTAGGCTTTGAGAGGGGCTCAAAGAAGGGGAGAGGGTGCACCACACTGACCCCCGAGCCGGGAGCCTCCCATGACTTCTGCAGGCCTTCTCCCCGACAGGAAGCTGC Homo sapiens hg19 +snp_rs10449246 snp_rs10449246 1 chr1 224936145 224936337 - ATTTTAAGCATATTCTTAAAGCAGAAGAAAAGTCAACTCCTTCTGTGACTATAAAAGTAACAACCCCTCATATCGGTATTGCATTTTCTATACTGCAAATTGATTTCATGTAAATAAGCTTATTTAGTATTCACATCAT Homo sapiens hg19 +snp_rs10185855 snp_rs10185855 1 chr2 101642110 101642302 - TACTCCTGGAGCCATTGGGGCCTGAAACGGCGCCTTGTGTATTCCACAAACGCGTTCCTACTGCTAAGCAGTGAAATTCACCCAGTGTTGGTGGGTTATTGTGCTCTAGAGAGCATTTGGTCTCTTCAGTGTTATTTTG Homo sapiens hg19 +snp_rs10184153 snp_rs10184153 1 chr2 182220015 182220229 - TGAATCTCCATGAGAAGAACACTATAATGGCCACATCATAAAACAATGAATAGCTAAAATATATCAGGATTGCTTCTTAGGAATAAGTGCCTAAGAGCTTTGTGTACTTAATTTCAATTGTAATAATACTAATTGATAATTACTATTCTGCCCATTTTA Homo sapiens hg19 +snp_rs10771328 snp_rs10771328 1 chr12 27425214 27425411 - TGAGGGGAAATCAAAAGGAAAACAAAGCATAATATTTAAATCGCATGGCAAAGTTCTTAAACTTTTGCACTAATATACACACCCTAGCTAATTCATCAGCATAATACCATACAGCAGATCACCTCAGTACTATCTTTCCTATACAT Homo sapiens hg19 +snp_rs11563675 snp_rs11563675 1 chr7 126873773 126873967 - GCAAGGTGTAGGGGTCTAGGCATAGCATTGTGCACAGCCACTGTTATCTGTTTCTAGAATGAGGTCAGTCTCTGCTGTATTACTTCATTAGGCTCAGCAAGCTAATAGACATGTGTTCTCAATGTTGGCCATTAGTCTCCC Homo sapiens hg19 +snp_rs10148795 snp_rs10148795 1 chr14 33845151 33845373 - TTACAATCAACCTCTGTTTGATCCTGTGTGTCTGTTTTGAGAATGGAGATTTTGGTAAAACATGCATTCTTGAGATAATTTGAAGACCAGTGAGATAATTCTTGGCAAACCACAATAAGATTCTCCAGTGAAACCAATTCCGTAAGTATGAAACATTAATCTCAACAGAA Homo sapiens hg19 +snp_rs10516506 snp_rs10516506 1 chr4 104595082 104595313 - TTTTCAAGGCTAAAATGTTTCACTTCCTTTACCTATTAACTACTCTGCAATAAGTCTATTGCTCCTACCTGGGAGTTTCTTTCACTTTTATTCTTTCTAACTCCTCCACGTTTAAGCCACCGTTTGCCACTCCCTTTTCATCTAAAACCTCATTCTCTTATAAAAAATGAAATAAAAT Homo sapiens hg19 +snp_rs10178199 snp_rs10178199 1 chr2 127756794 127757018 - CCAGGCCTACCCACCACACCCCATCACTTCCCTCTGGCGTCCCTCTTGTTCGCTCTGTGTAAAACTCAATTTGCCTCTTGATGGATATGAATAATTAGAACCCTCCAGCATGAATAATTCTAGGCAAATTAATTTTCATGCCAATCAGGGAAAATTAATTGGCTTCATGATG Homo sapiens hg19 +snp_rs10516603 snp_rs10516603 1 chr4 115467309 115467500 - CAAATAAGATTCTATGGTGAAGGTGCGTGCATCAGAAAGACAATTTAAATGTGAGGTGGGGGACAATGGTATATGTAAACACTAGCGGGGCCAGATGAATTTAGTATTTTCGGATAACAGTGTCCGCTATGTATGTCT Homo sapiens hg19 +snp_rs10088698 snp_rs10088698 1 chr8 48654620 48654821 - TTTGGCAGGTGGGACACCCAACCCACAGAATCCAATTCTTGTTGTCAGTTCTGGCTACTTTACAATCTGGGGACTCAGCCTTTTAGATTCCAGAAGCTGAAGTGCACATAGAAATTGTTACCAATCACAGCAGGTTTCAATGACATGCAC Homo sapiens hg19 +snp_rs10103826 snp_rs10103826 1 chr8 135495908 135496102 - AGCTGCCTTTTAGCACGAAGAGAGCCCAGCAAAGTGCCGGTCCTGACAGTGATCTTGTCCAGACTCCAGAACACTGGAGACAGCGGAACAGCAGAACACGGTGCCTGATTCAGTGAATGATTTCTGCGTCCCAGGGGTTAAG Homo sapiens hg19 +snp_rs1042606 snp_rs1042606 1 chr10 112270522 112270712 - CCCTGTAGGGTTACTTTCCCAACTAGACGGTGATCAGCTTATGCCCCGAAGCAACAGAGACAGACATTGAAACTGCCAAAGTTCAAAAAATAAGGTGGAAATTGTGCTTCCTTCAAAATGAATTGGCTTCATAACTGC Homo sapiens hg19 +snp_rs10497276 snp_rs10497276 1 chr2 166856843 166857041 - ATGCCCCAGGACAAGTAACAAATTACTGTAAGTTGTTAGCCTGAGTATCCTTCATCCTGTGAGTGCCAAGTGTCTGCTGTACTATTGTTCACATTTCTTATTCATATTAACTTATTATCTTCAAGAATTTCAGAAAGAAAATA Homo sapiens hg19 +snp_rs10753764 snp_rs10753764 1 chr1 167760563 167760807 - ATGGGATTAAGATTAGTACAATTACTGTTAACTCACAGAAATAATAGAGAAAGAAATGCAAAGTGCCTGGCTCACACCAAGTATTTGGTAACTACTAGTTACTTCCATTCATGTCACCTGTCACCTCCACCCTGTGGCAAGCTCCTTGAGGAGCTTTGTCTTGTTTTGTTTCCTTATGCTTAGCACAGTGC Homo sapiens hg19 +snp_rs1002745 snp_rs1002745 1 chr10 82656133 82656340 - TTTTCTCAGTGGAGATGGTGTTTTATGACAGGGAACGGGTGAATTCCTCTCCTGCTCCACATTATAAAATCCTGGTCAAAATATCTATAATAAAATGCAAGACGAAAGGTGAGCAGTGAGGCTGACAGCTGGAAAGGGCCAAGAGTATATGCTTT Homo sapiens hg19 +snp_rs10073948 snp_rs10073948 1 chr5 82134466 82134661 - TCTGTCTTCTCAGCGTCCTTCTGATGTCCAGCTTTGTGTTTCCTGCTATGGACATTTCCTGAGATCACTTGAGCTTATGTTCCATCTCCGAGAGAAAGCTGATGAGAATTAGTCATCCATGAATGTGATTATGGGTGATAA Homo sapiens hg19 +snp_rs10830004 snp_rs10830004 1 chr10 133212057 133212291 - AAAGTAATCTCATGATTACTAGTTACCCTCTGATAGGTAATCGCTTTTTTAAATGGTTACAGTGCAGGCACTCAGAACTACTTTTTATAGCTGGGTGCCATGTATTTTTCTGGAAAGATGAACCGAGGAAATGATTTTCCAACTGTCATTGATATCTAAGGAAGACAGTGTGTCCACTGGGG Homo sapiens hg19 +snp_rs10128762 snp_rs10128762 1 chr12 74681738 74681939 - ACAAATAGCTTGTTTTTTAAAAGGACCTTTGTGAATGCATTTCTTATTAAGCCAAATGACATTATAAAATTACTTGCTAATGGATGCAGAGTTGCTGAAATGGTGAATGTTTGTCCCTATTAATAAAAACTGGAAGTAGAACGAAAAA Homo sapiens hg19 +snp_rs10109209 snp_rs10109209 1 chr8 5528789 5528981 - TACTAATGCCTCACCAGACTTTTGCAGTTCCTAACAAGTGGTCTTTCTGTTCTTGTTTTCACATAAATCTTCATGGTAGAACTTCAAACTTATTGCTCCCCGCTGTAAAATTACCCCTGCTTCTCACGCCCCAGCCCACG Homo sapiens hg19 +snp_rs1026580 snp_rs1026580 1 chr10 13980998 13981214 - TAGAATAATGTGAACCATACGGTTGGTACTGGCGTTGAATTCCCTGCAGCTGTTTCAATGGTCTTGCCTTACCGTGTAGCTGCCACTTCCTCTTAACCCTCGGGTTTCTCAATCTTGGTACTATTGACTTTTCAGACCAGATCATTCTCTGCTGGAGGGTGGG Homo sapiens hg19 +snp_rs10505299 snp_rs10505299 1 chr8 118426572 118426777 - TCTGGAATATAGAGTAGGGACCTAATGGGAGAGAAGACAGGAGAATTTGGAATGTCTTATGGGAGACATTGTTTTTGGATGGGGATCATGTAATATATTAACAAATAAGAAACAGCTAAAGGTTTTCTAGAAGATGACATGATCAAAAGTGTT Homo sapiens hg19 +snp_rs10919336 snp_rs10919336 1 chr1 170216650 170216862 - TTGCTTTTTTCTATTCCTCTTCTTCACTTCAGAGTTGGCCTAATCATGGCACAAATAAAGGAGTACTCTGTTCCACATCTTTTATGAAACTTTTGTTCCATTTACAAAATGGAGGTTATTAGTCCTGACTCTTGATTCTTAAGGCAGATAAGAATT Homo sapiens hg19 +snp_rs10505532 snp_rs10505532 1 chr8 130021793 130022003 - TAGTCGTTACTGATATGATACCCAGAGGGAAGATTCCTAAACAACCACCAATGAAGTCATTCAAAGTTAACTGAGTTATTCCCTTACCAAGAGTGTTTTGTATTGTTGCATTATGTAGCACCACAAACTTAGTGGCTTAAAACAATGCAAATTTATT Homo sapiens hg19 +snp_rs10518287 snp_rs10518287 1 chr19 35399234 35399459 - AAACACACATTTGCACCTGCAACAGATGTGCTACACCCAGTTGAACCCCAGGCACTCTGACTGAGGTCATAAGCTTTGTATTGAAGTCATCTGTCTCCAACCAGAGGTATGGCACTATCCTCTCTGATAGCAAATCAAGAGCACAGTGCTGGCATCTGGTGAAGACCTTCTTGC Homo sapiens hg19 +snp_rs10955157 snp_rs10955157 1 chr8 99226982 99227217 - AATTGGTGAAATGGACAGAAATTAGGACACCCAATGTTTTGATGGCTGTTTTAGGGAAGGCAAAGAGATACGAGTTTAATAGCTTTTGTAGCACTACTCAATTAAATCAAAGGTCTGGCAAATAAGTCCCATAAGAAACAGTTAAAATAATTGGTTTAATTTACCCGGAGAAGAAAAGACAA Homo sapiens hg19 +snp_rs10487324 snp_rs10487324 1 chr7 110036449 110036638 - ATCTTAAGTGGCGACTCTCAGGTTCATTTCACAATGAACTACATTTAGCATCCAGTCCAATGACATTTCTGAACTTTTTTCATATTGATCTTCAATTTTGGATCATACAGCAACAGTATAACTGGGTTTATTCCAGA Homo sapiens hg19 +snp_rs10519096 snp_rs10519096 1 chr15 61289759 61289993 - TGTGGGTTTCTGGTGACAAAATCACTTTTTAGAATCTTCTATTGTAGAGATGGGTAGATGGGACAGCAGCAACATAAATTTGAATTTTTTTTAAGCCATAACTATCATGTGGAAGATATACATGGGTGCTTTCTAAGAAGATAAATGTGAGTATTTGAGTATATCAGTAGACTATCTTAATTT Homo sapiens hg19 +snp_rs10968281 snp_rs10968281 1 chr9 28013135 28013339 - TAAGTCAGGCTTGGAGCAGGAGGAAAAGGTGAATAAGAGTGAAGAATTTAAAATACATATATAAAGGAGAAGAAAAAGAAATACAAAGACCAAAAGTGGAAGGCAGAAATAGGGAATTCTATGTGCCAAAATGTCTTTTATCATCCCTAAA Homo sapiens hg19 +snp_rs11060670 snp_rs11060670 1 chr12 130515566 130515760 - CCAGGGAGCCGTCCTGAGCAACAGCTGAAATCTCCTTCTGCAGCCTTCACATAGGAGAAAGCCGTCCTTGTGATGCTTCTGTTCGCCGTGGAAGGGATCTGAGTCTGCAGCAACCTCAAGTCTTGCCTCCCCAGAAAAAAGA Homo sapiens hg19 +snp_rs10859402 snp_rs10859402 1 chr12 93409694 93409895 - AGCAAAACAATAGCATCACTGCCATTCGTGCCTCAGCTTCATGGTGGGGCGGTAGGAGAATGTGTGTTTTGCCTGCTTTGTTGCAAGGAGGAAAGGGAGGGTTGCTCTGTCCTGGTTGAGGAGGCAAAGGTGGCATTCCTGTATTTTTGT Homo sapiens hg19 +snp_rs1108958 snp_rs1108958 1 chr13 51822032 51822226 - TATTCTCATTTGTATGCAGTTATCTGATAAGCGTGTGCCCCCATATAGACCTGAATCATGAAAATTCATCATGATGGCTAGGAACACAATCAGAATTCAGAGATAATTCTGGCCCTTTTCTTTGCTTGCCCTTTCTGCCTGC Homo sapiens hg19 +snp_rs10869756 snp_rs10869756 1 chr9 78959172 78959384 - TCATGTGCTGGAGTCAATTGTGAATGGGCACAGACTGGGAACCATGATATGGTAGAGTTTTTATGGAGTTGCTTTAGGGGCTTCCTGGGAATGGTGGGTGGTGAGGGGAGCATGGAGAGGCATCAGATGGGGTTCTGGGGTGGCTCCTCTGCTCCCACC Homo sapiens hg19 +snp_rs10502370 snp_rs10502370 1 chr18 8454350 8454541 - CATTGGAACCACCATCTTTGAAGAGTGTTTAAGTTCTGTGTAGAGGTGTTGGGGTCTTTTATGAAAAGCAGAGGCCTGGCCAGGAAGTCAGGACGACCACTACCCATGTCCTGAGAAGGTGACCCAAATTCACTCACA Homo sapiens hg19 +snp_rs10000030 snp_rs10000030 1 chr4 103374004 103374198 - ATCTTTTCTTAAGCCCGCTGTAGTTAAACCTGCATCATATTGAGCCAGATAGAATCTCATGAAACAGTCATATCAAACAATGAAACATATGGCTATATGCAATTCATAGTTTATTCTTATTTTTAGCAATATAGACTTT Homo sapiens hg19 +snp_rs10746432 snp_rs10746432 1 chr1 210837539 210837734 - ATCTGATAGGGGGAAATGATAAGGTGGCTTGGCAGCTGTATTTAAATCTTATTTACTCTAGTAGTTGCAGTCTGGAGATATCATGGAGTCATTCATCAAATGGCCCTAAGCCTGCAGACCTTCCTCCAGAGCTAAATTTA Homo sapiens hg19 +snp_rs10438441 snp_rs10438441 1 chr15 92862458 92862657 - AATCACAAACCCTGCCCTTCCAAATTTGCTAGCCACTTAGCCCTTGTTGGAATTACCGTACACATGGGGCAACAGTCACGCTGTGGTTCAGGGAGCCCTCCGAGCCCAGGGCTTTCCTTTCCCTTGGTGCCACAGTGGAGATGCTG Homo sapiens hg19 +snp_rs1110240 snp_rs1110240 1 chr1 21324778 21324997 - TTACATTTCTTTGTGCTTTATTCTTAGGTAACAATAGGTACATATACACAGTGCTTTGCTGTTGTCTATAGTAATTAAGAGATTTGACTTATTTACTCTTTTTTCTTATCAAGCCTATAAGAATACCACTTGGATTAATCATGTTAGAGACTGATGTTCTTTACTA Homo sapiens hg19 +snp_rs10110604 snp_rs10110604 1 chr8 16502925 16503123 - AAAGTAGAGACTGTTTTGGCTATGAAAATAGTCCTGGTCACAGCTCCCACCAAAAAATGAAAACTTAAAAATAATGATAATTTTAAAAGCTGGGATGTATTTTTTAGGGCCGAGGAAAGTTTCGCACTGAGTTACTTGAGATAATG Homo sapiens hg19 +snp_rs10502432 snp_rs10502432 1 chr18 19827323 19827515 - AGACAGAAATTGAGTTGGAGATCCCAAGGCCTTGACACTGCCTTCCTGTCAAGGGGTAAGAACTGTGGCGATGAGAGGGAGGGGAGAGAGAGGGGGCAGTGTGTGCCACCAGCTTCACCTGCCATGGTTGCCTCCAGCC Homo sapiens hg19 +snp_rs10874743 snp_rs10874743 1 chr1 91951952 91952160 - CAAGAATACTATCGAATCACTTCTGCACAAACTTAGTTGAGGTCTACAGGAAACAAGCAGCAGCAGCAGTGGCTGAAGTGAGAGGTCTGGCTGGTAGGATTGAAGTGGTGCACTGTCCAGAGCTGGGAAGGGTTTGAATTTTACCCTACTTGCAA Homo sapiens hg19 +snp_rs10090419 snp_rs10090419 1 chr8 124028479 124028669 - GGTATCAGATCATGCTCTCTGCCTTCAAGCAAAATTTTAAACATTAGGATCTGCTAAGTGGAATAGGTTTAAACACATTCTCAGTTTACTAATAAAAGAGTCAAAGATGGGAAATAGTTGGAAAATACTATTGAGAGT Homo sapiens hg19 +snp_rs10496687 snp_rs10496687 1 chr2 133269105 133269307 - TTGCTGTTATTTACCAAGACAGCAAATGGTCCTGCACCCTCACCTGGCTACTTTAGAAAAAATCACCTTCCGCAGCAAATATGACACTTCTCTGATTAGCCACACCACAAGCTTGTCCAAAGAGTCAGAGTTCTCCCTCAGCACTACAT Homo sapiens hg19 +snp_rs10790037 snp_rs10790037 1 chr11 114665009 114665207 - CCCAGTATACTGAGCACTCAGGACATGCCACAAGATGATCTGGAAGTGAAGGGGCACCTAATTCATCATGATTGGGCCAACTAAATGTCCCCAGAGGCCACACTAAGCTGAATCTTGAAAAATATTATTGCAATATGAACAAGCAGG Homo sapiens hg19 +snp_rs10895457 snp_rs10895457 1 chr11 103416499 103416695 - TGAGGGTTACCAAGTGTAGGGAAAGAAATTCATGATGGATTTCACCATTGCTCCCAGGATAGCTCCAGCCTGGAACCCAGCAGACTCACCATCAGGACAAGGAATGTGGCTTTCTGATTTAAAGATGAGAGCAACTAAATTTA Homo sapiens hg19 +snp_rs12604608 snp_rs12604608 1 chr18 42405927 42406123 - TATTGGCCTCTGTTGACCTTCCTTGAGAGACGACATGACATTTTCAATCACATTTAGTTACAAAAAGATTCATCTAATATTTATTGAGAACCTACTAAATTCCAGGTATTATGCAAGTCGTTTGCTTATGCATTTAACTCTT Homo sapiens hg19 +snp_rs11171681 snp_rs11171681 1 chr12 56193075 56193282 - CTTTCTGATTTACAGTGGAGGATGGGAGGACAAAGTGCTAGAATGGAAAGTAGATCTTGATTTGTTTAAACTGTTCCACAAGGGTGATCCTAAACATCTTTAATTTGGGGCTTTTTCCACAAATGTCTGGCCATTTTGTACTATAGTACATTAA Homo sapiens hg19 +snp_rs10961505 snp_rs10961505 1 chr9 14410433 14410646 - TTCTCTGAATCACTCTCAACTTTCTTCCACCACAATCTAAGGCAAGGCTGATTTTAAAGTACTTTTTCATTTCCCTTTTATTTTTAGGAGGTTACCAGAGGCAAAGGTAATCATGCTCTGATGAACTGTAACTCTTCCCAAATCTCCTAACCTCTTCTA Homo sapiens hg19 +snp_rs10497933 snp_rs10497933 1 chr2 212141525 212141718 - TCTTTCATGCCCATCTTTTCTCTTCCCTCCCAGAATTATTCTTTGTCTTCTCTGTGGTTCAATGACATGTACCTCTATTATATCAGGTTTCATATTCTTCACTAGATTACAGCTATTTATACATGTGTCCTTCCTTTTCAC Homo sapiens hg19 +snp_rs12587583 snp_rs12587583 1 chr14 69510292 69510482 - GAGTCACAGCTTAGTTGTCTTAGAAGAGCAGAAGTAGGAAGTCAGAGAAAGACGAGGGCCTCGGTGGGGTGGAAAGTGGGGGTCCCAGAGAGCATGAGGTAGTAGGAAGAATGTGATGTTTAATCACAGTGTGATGCTTTG Homo sapiens hg19 +snp_rs10966009 snp_rs10966009 1 chr9 23651277 23651483 - CACAGGGCCCACAATCATCGGACACCTTGCGGCTTTTGCGTGAGCTTATTCCTGTGTTTGGAAACGCCCCTGCCTTGTCTGTACTTCAAGAATCAACTTAAGCTAGCTTCATTCTCCCATTTCCACAAAAACTTCCAGAACTCTGTACACATTTC Homo sapiens hg19 +snp_rs1160246 snp_rs1160246 1 chr9 119992935 119993131 - GTGGAATCTTTCGTCATTGCTGATGATGCTACCTTTCCATGATGCATGCACTGTCCGCTCCCTCTGCCCCAGAATAGCCACTGAGGAATGAGAAAAGAGGTCTTATTTTCATTCTCTCTTAGACCTTTTCTTTCCTGGCTCAAT Homo sapiens hg19 +snp_rs11096672 snp_rs11096672 1 chr2 20743564 20743772 - CGGGACCAGCTGTCTCCACCAGCTTCTTTCGGAGGCTGGGTAAAATGTGTAAGATGCTGGACCAGGGAAGCCACTTGATTGCCTTATGTCCAGGGCACCTTCCAGACCATAGAGGCCTGCCACAAATCCCTGGGAAATTCGCCTTTATTCTGCAGC Homo sapiens hg19 +snp_rs10926264 snp_rs10926264 1 chr1 235778986 235779175 - CCCATCCATCATGGACTGCTTGCCATCCAGTTCACTGTGGCAGTGCTGAGGGCTCATGTGGTCCAGGTCCCCATTCTGCAGCTTCTCCATCACCCCCCTCCTCCTGGTGCTTCTTGGAAGGAAGCCTCTCAGAGGCA Homo sapiens hg19 +snp_rs10050018 snp_rs10050018 1 chr4 183349468 183349656 - ATCTTTGGGAAAGTGAACGTGGAGATAAAATGGGAACATCAGTCAGCAGTGGTGGCGTAAGCAGGAGAAGCAAAGCACATGGGAACTAGACAGGTGGCTACAGTGAGGTACCTATGGCATCTCTTTATGCTCTCT Homo sapiens hg19 +snp_rs10243669 snp_rs10243669 1 chr7 45915758 45915965 - TATCAGTCCTTGTGATAGAAAATAATTACACTATAGGAGGTCAGGGTTCCTCACCAGGTAAGAGGGTTGTCATGGTAGTCATTTGAGTTACTGTTTTCTTCCTTGTGCTCAAGAGGGCCCTCTGGGAAAGTCATTGTGGTTTCTTCGTCCTCTACA Homo sapiens hg19 +snp_rs10767843 snp_rs10767843 1 chr11 30436224 30436446 - GGACCACAGGAGCAACCTAGCTTTCCAAAGCTTTGGTCATCCGGAACCACAAGGGGTAAGACTTAGTGTATCTAAAGAGAGCTGGGTATCTTGTGACCAGTTTACAGGCAGCTCCTCTCAGTCCTTCTTTGAATCATCTTAGAAGTAAACTGCTATAAGAAAGATATAAT Homo sapiens hg19 +snp_rs1040173 snp_rs1040173 1 chr2 146120361 146120549 - TCCTCTACTATAGCACGTATTGTTCAGAGGATCTCATATGGCATCAATTAGAGGGCAGACCTTGGGCTGAGGCATTTGTTTTCTGCTGACACCTTTTGAAATCCCCATTCCTCATTCACTGGTGCTCTAGTTTTTA Homo sapiens hg19 +snp_rs10490012 snp_rs10490012 1 chr2 234843344 234843570 - AAGATGGTAATAGTGATATGCATTTCTATGACTTTTCTAAAAACACAATAGGAGCAGAAATGAGTTGCTTTATGGGCAAATTTTATGACCAGTCCAGAAGCAGATGGATTCCCAGCCAAACTGTGGCCAAGTTTCTGCTGCCTGAAAGCAATTGGCTTCAACTGGAGTTGCTCT Homo sapiens hg19 +snp_rs10500844 snp_rs10500844 1 chr11 19250005 19250225 - ACTTCTCTCTGTCTTATTTTTCCGCATCGGTAAAGAATTTATTCCACCAGTTTTTCCTCATCACCTACTGGATATAAAGCACTGTGCTCTGGATCAAATCTAACCCAGCACCTGCCTTTGGTGGCAATTGCTTTTGGGTACTTGCCTGTGGGCATATGATAGTTTTT Homo sapiens hg19 +snp_rs10143478 snp_rs10143478 1 chr14 33442462 33442696 - AAAGTACATTTTTAGATGAAACTTGGAACACTGTTTTCAAACAAATGACTTTTTAGATTGTAGTTAGGTGTCTGATCAGCCCCAGATGCCTGTTTAACCTTAACATGGCAGAATAATGGACCATGTATTCCCAGAATAAAGACTAAGTCAGTGAAAAGGAAATTTTAAAAAAATTAATA Homo sapiens hg19 +snp_rs10493230 snp_rs10493230 1 chr1 58049953 58050179 - TCAGCTATGGAAGGAGCACACTATTCCAAGGACCCAGAGAGATCTGCTGCATCTTAGCAGACACTGTACAGAGCTTAAGGCCTCAACCAGCCCTGTGATTTGATAAAAGAAAAACATCAGCCAAATTAAATTTAAAGGAGTTTAATTGAGCAATGAACAATTTGTGAATTGGGC Homo sapiens hg19 +snp_rs10489562 snp_rs10489562 1 chr1 96058387 96058598 - CCAGGCTGTCTACTGGCTGGAGCTAAGCTAAACACTTGTCACCCTTCTATAAGTGCAGGAAAGATGGCTTGGGAAACCTAAAGAGAGAGAAAAGTGTTTCAACAGAGTTATGATCACACAGTGAATGAAGTTTCTAGAAATGGTATAATGCAGTGAAAA Homo sapiens hg19 +snp_rs109894 snp_rs109894 1 chr5 79067918 79068134 - ATAAATTTTTGCTTAGCCGGCCCCTAATATGCTTGCCTGCAACAAGAAAAATAAAAATGAATTGATTGGCAAGATCTCAAATAGAATAAGCTAATGACAAGCCTTATGTTTTAATAAGCTCGATGTTGGTCTTAATGAAATTGGTGGATGGTCTTTTTTTTTT Homo sapiens hg19 +snp_rs10914880 snp_rs10914880 1 chr1 34620621 34620809 - CATTAGCACTTTATGATCACCTCTCTGTGCAAAACTTCTCTCTTATTTACAAAGTTTGCCTCCCTTCATCCCCAATCCTGAAGCTAAGCTATCCCAATCCCAATAAGTACTCATTCTGATGTGTTTGATATATGTC Homo sapiens hg19 +snp_rs11662069 snp_rs11662069 1 chr18 29829195 29829384 - GTTCCCCATCTTTCCGTTGTATCTTTTCAACAAAGGTTCAAAGACCAAGTATAGCTTGAGCCAAAACTTCGGGGTGCTTTCATCTGTTTAAGAACTTGAAATCTTTATCCACTACTAACTCTGTCCCTCTTGATGCCAA Homo sapiens hg19 +snp_rs10996274 snp_rs10996274 1 chr10 66956996 66957203 - TCTGTCTGGAGAGTACATGTTTTTACTCCCGTCTAACAATGAACACCTTTCAAAACATACTGAGTTTACTCCATTTCATGTTTGTCATCCCTCTATTCTTTCAGACCTGTATTAATGAGCTCAGGTTGCCATGATAAAATACTGTAGACTGGGT Homo sapiens hg19 +snp_rs10849968 snp_rs10849968 1 chr12 109694168 109694359 - GAAGTTTTCTGGGGAGAGCACCCAAGGCCACCTTCTGATGCCCAAAGGGGTTGTTAGCCCTTGTGGCCTGGGGACTGACTACAGGGTCCCAGGCCTCAGGAGGAGGCTGGCTGAGATACCTTCTAAGGGCACACACAGA Homo sapiens hg19 +snp_rs10496397 snp_rs10496397 1 chr2 106184288 106184481 - CCAGACGCTCCCTAATGGTTTTGCCTGAGTCTCTGGCATCAGAATTGGCAGGTTCTTGTCTACAGGTATTGAATGCACAGGGTCTCACTTCTTACTGAGAAACTACAGACACAGGGGGCAATGAGAAAGGAAGAAGCCCC Homo sapiens hg19 +snp_rs10744116 snp_rs10744116 1 chr12 16476721 16476917 - ACAATCTTTGTCTCTTAAGTTCTCCCAAGGCCACACCTAAAAAGGGGGTTATGTTACCAGTGTTTGGTGTCAGTATCACGGAAGCCCAGGCATTATTTTAGTCTGTAGTTGCCAACATGCTCATTGCTGGTTGAACAGGTCAGTA Homo sapiens hg19 +snp_rs10521575 snp_rs10521575 1 chrX 116625894 116626091 - TAGCCTTAGAAGCATCATGTATTTCGAAAGTGGTATTTTACCCTTCATTAAACCTTGTATTACAAAGAAAAAGCTGTCTTTGTGACATTTAAGTAGGAAGATGTTATGATAATATTTAATGTCTAGAGACAGACAGACAGGATT Homo sapiens hg19 +snp_rs11104117 snp_rs11104117 1 chr12 87224875 87225091 - AATGATTCGAGCTTCAGAAAATGATCTACCAGGGATTTTTCTTTCTTCTTTTCGATTATCATTGTGGGTTCAAGGTTGGGAATATTCAAGGAAAATGGATATCTTTATGAGAATAGGTAGAATTTACATGTAGAAATGAAGATTAACATGGCAAATTATTGAA Homo sapiens hg19 +snp_rs1060912 snp_rs1060912 1 chr6 52389558 52389764 - TCTATTTGCATAGCACCTTACAGTGTGTAGCTCTGTGAGAAAAGGTAGATGGTTTTATCCCATTGTTCAGAAGGGTTAACTGAGACAGAGGGACCCTGGGTCATATGACAGACAACTGATGGCTCCAGAAGTGAGCTCCAGGTCTTTTCATGC Homo sapiens hg19 +snp_rs10865643 snp_rs10865643 1 chr3 69099573 69099803 - AACTTTAGATAAGATAGAATATAGGTTTTACATATAAGGATATTTGTTTTCGGAAAATGCCCATAGTCTTCAGAATGGTATAATTTAGATGGATACCAAATAACCCTGGGATTATATAAAGTATTCTCCAAGAGGCAAAATTAATTCCTGTCATCTTTTGAATGTATTTAAATTAAT Homo sapiens hg19 +snp_rs10153199 snp_rs10153199 1 chr16 860524 860710 - CCTGCTCCAGAACCCAGAGGTTCCGGGCCAAGGGCGCACACGGAGTTTGGGTTTGTGCTACTTCCCTGGGACATCCTGATGTGGCCTGTTTGGGAGAAGCCGCCAGGAACACCCTATCCTGTTGGCTCCATGTCCC Homo sapiens hg19 +snp_rs1002897 snp_rs1002897 1 chr2 66464173 66464394 - TTGTGACCCGTACCACTGGCCTGTCTGTTAAACAGTGATTACAGTTTATCTTTTCAAAGTCAGTGGGCAGGACCTACTGCTCTCTGAAGTACCTCTCAATTCTAGAACCTGAAAGTCCAAGTAAAAAGAAATAAACATTGTACTAGAATAGCGCCTTTTTTTTTTTTT Homo sapiens hg19 +snp_rs11113551 snp_rs11113551 1 chr12 108248152 108248371 - ATATTTCCGAGCACAGTTACTGCTTCCAGAAAGATGTGCATATAGAGCCCTAAATGCTAAAAGCAATGTATGGCACACAAATAATTTATGATGTGCCCTTTTCTTTCACTAAATTCAACATGTATTAAGGAAGAGCAGTTTCTAAAGAAACAACTTGTTAAATCTCA Homo sapiens hg19 +snp_rs1030356 snp_rs1030356 1 chr4 141826627 141826819 - TCTCCACCCCTTTCACTAGAGGAGCAGGATTCAGCATGACATCGCTCTGTTCATTGACAATTTCTTTACCAATTACCCCATCTTCTTCCCCTTCTTTTCCATTTTTATTGCCTCAAGATGGGTGATGGGGTCAAGAATTA Homo sapiens hg19 +snp_rs11048057 snp_rs11048057 1 chr12 25623812 25624027 - CAAATCCCTTGGCTTATTTTCTACATCTGCTCTTTTTTTCTACATCTGCTAATGTCTCCTTTTCCCAAGGCATGAAGGTGGAAAATCCTACATGCTTGAGGTGAAGAAAGGGCCTTGGGGTACAAGTAAATTCAGAGGAGATACACACCAGTGCTGGTAAT Homo sapiens hg19 +snp_rs1156232 snp_rs1156232 1 chr4 126433063 126433260 - TTTCCAGTTTCCTCAGTTTCAGTTGTCTAAAATTGTTTCGAAACCACTGAGTTTTTATTTTCTTTTAAGCAGAGGTCAACAATCAGCCTTCAGATGGTTCAAATTAGTCAACATAGATCAGAGCTGAACCCATGCCCTAGAAGTGA Homo sapiens hg19 +snp_rs11074037 snp_rs11074037 1 chr15 92604308 92604497 - CCTAGACTCATGGAAGGAGAGGGGAAACCCAGAAGAACAAGGATCATTTATTAGGCACCTATGTATACCAGACCCCAGTGCAAAGGTAGAAAAGAGGGAAAATGCTAATTCACAAACATTAATTTACAAACACTTACTC Homo sapiens hg19 +snp_rs10257276 snp_rs10257276 1 chr7 136370660 136370850 - AGATTCTGGTCTGGTGTCCTTTCTGCTATTACACACCAACTTCAGTGCTGCAAGATATTACAGCAGATGTGTTGCGGTTCTGTCTGGCATAACTGGGAGTAGCTGAAACTCAAGCAATTTGGATGTGCCCGGGGAAT Homo sapiens hg19 +snp_rs12588458 snp_rs12588458 1 chr14 67830703 67830911 - TCCTTGAATTCACAATGTCTAGCTTCTCTTATCCCCAATACTCCCAAATATTCCTTTCTTTTATTGAATAGGTATACCTAATCTTGAGAATAGCTTTAATCTCCATTACTACAAAGTTCAAGTTTCTCTTAACCTCCAAGCATTAAAGATATTTA Homo sapiens hg19 +snp_rs10077711 snp_rs10077711 1 chr5 179587592 179587795 - GTGCATGGCTTCTTGCTGATGTGAGACCCTTACTGGAGAAATACTCTTCTGCTTGCTGTTTTCTCCACTGGGCACCTATCTAGAAGTTAATTTTGTATTTTTCAGCTTTAAAAGTTTTCCTAATACTGATGACATGCATATTGTGTGTGGC Homo sapiens hg19 +snp_rs10279558 snp_rs10279558 1 chr7 114862779 114862986 - CAGATCAGACACCCCAAATATTGAAATTAGCTTATTCTGGAGTTGAGTTTGCCCAACTTCACATATACTTATGACACTGGAAGGTCAAAAATTGATCTCTCCTATTCAAGTCCTATAAAAAATAATTGTCTACCACCTAAGTTAATTTCAAGTT Homo sapiens hg19 +snp_rs10508853 snp_rs10508853 1 chr10 37069230 37069440 - TCCACTGAAGCCCATTTCTATCAAGTATTCTCTCGGCCAGAAAGGGTAACACCCGATATATACGCCCCAATTCCTTCACCTTTGTGCACAAGCCAGCCTTACTATTCAAATATAGAACTACCCACTGAGCCAGAACATGACCTCAGATCCTTAGAGG Homo sapiens hg19 +snp_rs10793421 snp_rs10793421 1 chr7 54704855 54705047 - ACATGTATTGTTTACGAACAGAAAATGCATGGTGGGATACATGTGAAAATGGCAAGAATGGTTGCTTTTGGGAATGGGGACCAGGGCTGGGGACTCATGTGGGAGTGAGTTCTTACTTTCCACTGTACATATTCCATGTG Homo sapiens hg19 +snp_rs10432009 snp_rs10432009 1 chr17 13091291 13091497 - ACATTATTTTTGTAATTTATTTTACCCTTATCATAAAATGCTTTTCTACAGTATGCTTTTCATAGCCATGTAGACTTTACCATTTTTGGATCTTACAATGAGGATTTTAATTTTTACATAATCCACCTATCAGTCCTTTTACAACTCAATT Homo sapiens hg19 +snp_rs11002643 snp_rs11002643 1 chr10 80478352 80478539 - AGTTCATTGCTGTGCTCACCAGAAAGTGGTCAGCAGAATGTTGCTTCTGGAGAAGTTAAGTGCAGGCTAGCAACTCCTCAGGGGTTCAGTGGATGAAAGGCTGCAAAATAGGGTTTGGAATCGCTTCATAGACAGGG Homo sapiens hg19 +snp_rs10519010 snp_rs10519010 1 chr15 60551765 60551969 - CCCAGTGAGTCCCATAGTTCAGTGGAGGAGTTTAATATTCTTGAGTGATAACTTGATGAATCACTCTTCTTTAGTGTCTGTGGTAGGAGTCAGCACTGATTACCTAGACCTAGAGTAACAGTCTTGTGGACAATCAAATTACTGTAAATT Homo sapiens hg19 +snp_rs11576172 snp_rs11576172 1 chr1 217324503 217324702 - GATTTTGACACTATGTCAAGGCTGTCCACTTCCGAGGACTAGACTCATGTTACCAGAGCTCATGAAAGACTGATGTATAAAACTAGGAGAGTGCTTCAGAGTGTGGGTGAGGATAAAACAAACTAGAGTTTGAATCCTGGCTCTG Homo sapiens hg19 +snp_rs11133601 snp_rs11133601 1 chr5 10104416 10104649 - AGTAGGGAAGGGAAGGAATATTCAATAAATGGTGTAGGAACAAATGGTAAGGGAAATAGGAAAAGAAATAGGGAATAGGAAAAAAGGAAATAGGAAAAAATATTCTTGTAAACCGTCCTATATAACTAAATACTATGTAACTAAGTAAATTCCAGTTGTATTTAAAAGTTAAATATAAA Homo sapiens hg19 +snp_rs10215963 snp_rs10215963 1 chr7 26583629 26583841 - CCAGCACCAGGCAGGAGAAATGAGACAAACAAGCTTTGAAAATAAATCTGACTCTCTCGCGGCTCCGGATAGCCGACAAGTGTTCGTCCATCTGCCGCAAGCGTTCACACTGTGAATTCATTGATTTGATAATACTCTCGCATAATTGATTAAGGAGAGAC Homo sapiens hg19 +snp_rs11265625 snp_rs11265625 1 chr1 153642759 153642954 - AGGGCTCACTGAGCCCCATCATTACTTGATGGGGGTTGGATTAACTTAGAGGAGGTTATGGGGGTGTAACTGGGCACCATTTGGAATGGGGACAAGTGTAAGTGTGAGTGGGGTCTCTTGCCTACCGTTGGGAGGTTCCGAG Homo sapiens hg19 +snp_rs10489391 snp_rs10489391 1 chr1 210458696 210458902 - CAGTAGATACTTAATAGTCAAAGCTGCAGGAAGAGAGCCTTTGTCTCACTTGAGTCAGGCACATCTAATTGGGAGAATCTAATTCTCTTCTAGAAACCTAGCTGCAAGGTAGTCTGAGAAATGAAGAGTTTAGTTTACCAGCCTCTGTAAATC Homo sapiens hg19 +snp_rs11024021 snp_rs11024021 1 chr11 16735341 16735565 - TTTTTATTATGGCAATTAAAAAACATATTCACACATGGGCAGAATCGTGAGTATGGACACCATGTGCTTAGTGGGGAAGTAAAACATTTTTGGCAAAGAAAAGTTGGATCACAGTTTTCTCCATTGGTTCTCCAAGTGACAGGAGCAACTTGAGATGATTTAGTAGCTGC Homo sapiens hg19 +snp_rs1034826 snp_rs1034826 1 chr7 108083455 108083662 - TACAAAAAAAAAAGGTCTAATTGTTTTAAATAATAGCAACGAGATTGTTTGGTAGGAAGATTCTTGGGATGAACACTGAGAACTTTACAATTCTGAGTTTGTGTCATTCACTGATCTCATTTTAATACATGGACCATTTGCCAATTTGAGGTTTC Homo sapiens hg19 +snp_rs10901226 snp_rs10901226 1 chr9 133483063 133483259 - GTCCAGAGTCAACTCTGAGCTGGCAGATGCTTAGGAAGGATAAATCATCTCCCTCCTCCATGCAAATGCTGGAGTCCACCCAAGGCTGAAACATGTGATTGCAGTTTCATTCCCTTCGGAACATTCCCATTTGCTGCCTAAAA Homo sapiens hg19 +snp_rs10997716 snp_rs10997716 1 chr10 53235867 53236086 - AAAACTCAATTCTTCAGGACTCCTGCAAATATTGACTGGCTCACGTCCTTGCCTGTATCCTTCAATACTGTAGGCCTCCGATCTCTACAGGTCTCAATTCCAAGGAACTTCCCATTTCCTTCTCAATGACTGTGATATATGGATGTCTTTTCATCTTCTAACTATT Homo sapiens hg19 +snp_rs10739688 snp_rs10739688 1 chr9 129772346 129772550 - GAGAGAGATGAACAACTAGAGCCTGGCCAGGTGTCCAGGCTCTGGCTCCAGCCTCTCCCCACCTCTAGCCTCCATGACACCGCCCCGTGAGGATGGCCAAATTCCTTGTTTGGTCAAGTTGGCTTGCCAGACTCACCTGGCCTCCCACTGTTC Homo sapiens hg19 +snp_rs10903900 snp_rs10903900 1 chr10 2990103 2990301 - TGTTTTCTCTCTTTATTTAGGTGAAGCATTAACAAGTCAATAGGCTTAACTTAGATATTCAGAATATGAAACCAGTCACTTAAAAAAAAGCTTTATTTTATTCAATAAAAAGATTGACAGATAATTATTACATCTACCATGTGG Homo sapiens hg19 +snp_rs10192459 snp_rs10192459 1 chr2 152517828 152518027 - TGCCTTTGATAACAGAGAAAAAGATGATTTGGATCTAAACGTGAAACAGTTGCAGAAAATAATGGCCATAGTTGTGCTAGAAAGATAGAACTGTATTATGCTAAGCCACGGAGCAAACCCCCTGGAGTCTTCAGAGAATTGAATGA Homo sapiens hg19 +snp_rs10860066 snp_rs10860066 1 chr12 97073116 97073344 - CCAGCAAGTTTATAATTCAGAGAATTTCTTGGTCCCAACCTAAAGCCGCTAAATTCAAAGCCCCCAGATCTGCAGCAGGTGTTTCAACATTCAGATCAATTTTTTTTTTCTTTTAGTATACCAGAAGGTCCTTTTAAAAAAAAAAAAAGCTTGGAAAACTTTTGATTCTTATGAA Homo sapiens hg19 +snp_rs10184780 snp_rs10184780 1 chr2 20054242 20054430 - GCCGGGCATTCCCAGCTCTTTCTAGGGTGGCGAGCTAAGGGTGACTAGACTCCATAGAATTGTGCCCAACCTGAAGCCTATTCCATTTGTGCCCAGCTTTGCTGCCTTGGGGCCTTTGCACTTACTGCTCCCGCTGC Homo sapiens hg19 +snp_rs11152428 snp_rs11152428 1 chr18 61994541 61994754 - TTTAAATGAACAGATATTAGACAGCCTTATAGGTTTTCCAGAAATACAGGGGAGAAGTTTTCAAAGGGCTTGCAGATGCTGAAATTGCAATAGGAAGAGAACCATATGAACAGTCTTGTGGCTGTCTTACTGAAAGGTAAAGGTAGGATTTTTTTCCCC Homo sapiens hg19 +snp_rs10925402 snp_rs10925402 1 chr1 237559299 237559489 - TCCTTCAGGAACTGTCAAAATTATATAAATGGGGGACCTCACAACCAAGGGTGATTCTCTATACAGCCATCCTTAACCAAACTTACATTAAAGTGCAAGAGTTATTTTTTCTCCGTTTCTTTCTTTCACAAATACGAAA Homo sapiens hg19 +snp_rs10111409 snp_rs10111409 1 chr8 133118324 133118522 - TTCTCCAATCCAAGCGCACATTCTCTTGACTTTTCTTCCCGCCCAATTCACCTTCCAGATAAATCCAACCCTCTACCAATGGTAAATTTCTCCTCTTTTCAAATCGTATCTGTGCAGCCTGTATTTAAATTGTCATTACATTAATA Homo sapiens hg19 +snp_rs1011539 snp_rs1011539 1 chr7 14294433 14294637 - GTGCCTTGCCACGTTTAAAAGAAAAACCCAGTTGTTTACACTACCCAGTGCTAGGGACATTGTTAACTCTAGGGAATGAATCCGAATTTGTGAATACTCATGGTAAGAAAATTCCTTACAAGGTATTATGGAAGGGCTGAAGATGGGGTAA Homo sapiens hg19 +snp_rs11084990 snp_rs11084990 1 chr19 3009070 3009261 - GCTGGAGTTTTCAGAACCCTGGCCTAGAGCCAGTCTGGGCATTGGATGGAGAACCCTTCAGGATCCTTGGAACCGTGGAGTTCTAGGATTTCCTGGATAGAGATTTTGGTGTCGGTGTGCTCAAGTGAAAACCTCAGCCC Homo sapiens hg19 +snp_rs10122609 snp_rs10122609 1 chr9 9283394 9283595 - TGTCATTTTTCTATTTGTTCTATCACTAGTGATAATTGGGCTTACTTCCTAGCAGTTGGATACTTTCTGTAAAAAAGAAAATATAAAGCTAAAATTATAGACATTATGCTGTGCCTGAAAGAGAAAAGAAATGAGAAGATATAATTGAA Homo sapiens hg19 +snp_rs10208207 snp_rs10208207 1 chr2 169074793 169075011 - CGCTGTCCTATGACCTGACCCTGGTATGCATGGTGCTGTGCCCTACGGTCACTATTTTTGATGATAGGACTTTGTCCAGTCAGCTTAGCGGAAAAGATCATACATGTTGAACACTGCGAAAGTGAACTTTCCCAAGATATTCTTTTGGGGAATTTTCTGAGCTTT Homo sapiens hg19 +snp_rs10954365 snp_rs10954365 1 chr7 131855009 131855207 - CCCTCTCCTTTCAGTTTACATCATGGTCCCTGGAGATGGCAGAAAGAAGTGCCAAGTGCCGGGATTTATGACCTCCTTCCACCCTTCTGTGTCTTGGGGCTTTGTGAAGCTCCTTATCCTCACAGGGTCCCTCATGGGGATTATAAC Homo sapiens hg19 +snp_rs11118109 snp_rs11118109 1 chr1 218632773 218632961 - GCAAGAACAATCAAGGGCCCGCACTGTGCTGACACAATGCTAGCAAAATTGTCACATTACCTTACACAGAGAGGGCCTTTCCGTTTATATGGAATCCTTACCAAACCCCTTGACATAGGCAGTGCTTATTAGCTTT Homo sapiens hg19 +snp_rs10168253 snp_rs10168253 1 chr2 180659424 180659615 - TGTTTAAGGACCAATTTCTTCTCTTTAATACCTAATCAGATCCTGCTCAGCGGTGTCCCCATCTCATCCAAGATGACTCCTGAAGTCACATTGATCCCTCTTTCCTCTATTATGATTGCAGATTCAAGGTAACTAGG Homo sapiens hg19 +snp_rs11118515 snp_rs11118515 1 chr1 220473871 220474090 - TTGTTTTCTTTTCTGTCTCCTGAAAGAGCTGTGCTCCAGTGTCTGCCCGGTAAAGTTGCTAGTGGCAGCATTCCTGGAAGCTCCTTGCTCCAGATGATGTCAGACCTCATGTGACCCAACCATCGCACGCCCGGAAACATTACATCATTCTAAGATGTGATTCCTTTTA Homo sapiens hg19 +snp_rs10133359 snp_rs10133359 1 chr14 26718991 26719190 - ACTGAAAAATTCATCTTTACATTTCCCACCTACCTTACCAAATGAAAGAATTACTAACTATTCCAAATGCAAGTTTGTTTTATTTCCTTTTTCACAGCAAAATCAGTCTATTATAATAATTATTTTATAAATGTCTCTTTTTTTTT Homo sapiens hg19 +snp_rs1038024 snp_rs1038024 1 chr17 25725450 25725643 - TCGCACACAGCTGGTGGGCTTCTGGGCTTCCTAACCATAGGCTTCCATTTTCCCCCATTCAAGTGAGACCATCTTGGTCCACCTGACTTGTCTGAGCCACCTCCTGGCATTAGGTTCCTGGTCCTCATGCCACTGTCACC Homo sapiens hg19 +snp_rs11144978 snp_rs11144978 1 chr9 79225176 79225367 - GCATGGAGATCAGTGATAAAGTTGGGAGCCTAATTAAAAATCAAAATCATAAGGGGCCTTTTATAAGCTGAAGTTAAAAATAAATAAAATGAAGACAACTTCAGTCGTGGAAGCCAAGACTTTCAGTCATAGATTACAG Homo sapiens hg19 +snp_rs10932037 snp_rs10932037 1 chr2 204825190 204825397 - AATGAATATTCTGCTCTACCCCATGAGAATGCTGGCCCATTAAAGATGATTTTGTTTGCAATTTTAATATGATCTACAAAAAGAACTAAACTTGTAATTAATAGCACCATGAAAACATAGATAATGGTAGAAAATAGGATAATAAAATAAATTT Homo sapiens hg19 +snp_rs11114607 snp_rs11114607 1 chr12 81157287 81157492 - ACTTGACACACGTAAAGAAAGTAAAGGTTGCGAGCTACCATGACAATCTATGGACACAGGCTTCCTTACAAGTTCTCTTTAGTCACAGCAAAGCAAGCTGAAAAAAAGAAGTTGGTTTTCAGTTTAATTTAGTGTGTATAAATGTCAATAAA Homo sapiens hg19 +snp_rs10058793 snp_rs10058793 1 chr5 4739659 4739860 - TATTCAGGGAATAAATAGAAACAAGGCCACCATGATAATGTTGTCGGTTCAGAGAGAGAGAGAGAGAGAATATACACATACACATATACATACACACACATATATTCATACATACACATAGTACAAACTATATCATGAATAGAAA Homo sapiens hg19 +snp_rs11017093 snp_rs11017093 1 chr10 131925950 131926165 - TGTATTTGTGGAGGCTCCACCGACTCACCCAAAACACGTGCTTTTCCCCTGACCTGCAAACTTTTAACACCTTCTTCTCTTCCCGTTTCACTAGGCTATTTGAGATCCTGCAAGATTTATCAAGACTGTACTAGCCATATGAAAGCATGTTAACACAGGGAGGG Homo sapiens hg19 +snp_rs1015077 snp_rs1015077 1 chr6 167526356 167526573 - ACATAATGCAAAATTACAACAAGTGCATCCGAGATTGTTATACAAATGGAATCGCAGTATTGTTAAATGACATAAATGCATTCACCCACAACACAGTGAAACTGATTGTCACTGGTTTATCACTTTCACTTGGGAGACAATGCTATCACTAGAACTCCTTCT Homo sapiens hg19 +snp_rs12785223 snp_rs12785223 1 chr10 104843861 104844061 - TAAAAGACTGCAAATGCCACGGTTAAATAAATTCAGTGGAGACTATAAATGGACCAGTCAAGAGGCTAAATTTTCAGAGCACGATCCTCTTTGGAATGTAAAATAGAGACTAAAAGTGGAGAGAAAAGGGATTCCAAAAAGATGTGG Homo sapiens hg19 +snp_rs10745558 snp_rs10745558 1 chr12 91910025 91910223 - CCAAGCTAAGCCAAAGTTAGGAATCTAGGAAAAAACTCCCAAAAGATGAACCAAGCTGACATCCATTTTTAGTAAGTAAAAATAACATGATTCATAGGCAAATGAGTATAAAGGTCCCGAGTTTCTGCCTGCTGCTTCTTAATT Homo sapiens hg19 +snp_rs10499441 snp_rs10499441 1 chr7 14505532 14505753 - TTTTTATGTTTATGATCCCTGGAAGTAGATGTACACTTGAAATGTTTAGGATTTATATGATAATTCCCCCTCCCTGTTGATGGCTCATTTCTGTTCTTAGGCCAGCTTGTGTGCACATGCAAACGTCTACTTCCAACTCATGCAAATCCGATGGATAATGCATCACA Homo sapiens hg19 +snp_rs11137287 snp_rs11137287 1 chr9 140382556 140382764 - GGAAAAATAAAAATAAATCCACATCAGAGAGCCACGTTCGGGCCGAAGCTCGGGACGAGACATCAGACCGCGAGAGCCGCGTTCGGGCCGAAGCTCGGGACGAGACATCAGACTGCAAGTGAAGCTCGGGACGAGACATCAGACCACGAGAGCAGCG Homo sapiens hg19 +snp_rs10489858 snp_rs10489858 1 chr1 19947099 19947295 - CCGTACCACTCAATCAAAAAGATGAGCAATGCTTCCACATCCATCAATATCAAGTAGAAAATCTTAATCTCTAGAATTCAGATATATGCCCAACCACCCAGTTTTGCTCCTATTATAGGCATTTATCTGCAAGTATAAATAT Homo sapiens hg19 +snp_rs10519980 snp_rs10519980 1 chr4 149634856 149635064 - AGAGACTCCCTCGTTGACCTGCTTGAGTGCCCCGTTTGAGAAGGTGCTCTCTTTATGCTAAAGAAGGACTGGATGTAGCAAAAAGGTTTCTGTGCTGAGAGCCAGAAAGTTGCCCTTGAAGTATCAGCAATGAAGGAAGAGCTAATTTTTTTTTT Homo sapiens hg19 +snp_rs10489924 snp_rs10489924 1 chr1 99458822 99459029 - TCTTCTCTCTGGCTCCTTATCACATGAATACTTGGGGTTCCCTTTTTATTTTTCCTGGGCTAAATCTAGAATACAGATATGAGAATCCAGTAGACACTTTTTTCAAGCCACACTATCAGGCTCTTTCTGTCATCCCATTTTTGGAAAAGATTC Homo sapiens hg19 +snp_rs11081675 snp_rs11081675 1 chr18 28580528 28580717 - ACGGTGAGAATAGCTAAAGAAGAGGAAAACAGCATAGCCTACAAGACAGGAGATGATAAAGTTTAGGGGCTATTTAGCAAATAATAAATAAATTGATTTAGAATAGAAGAAATCATGTGTTGGAAAAGAGGCTTGAA Homo sapiens hg19 +snp_rs10183112 snp_rs10183112 1 chr2 38445612 38445817 - AGGAAACCATCAGCCAGAGGCACAACCACAGCCATTGTCTGCTGTTCCCTGCCAAACCTCCACCTTTCCTCTGTCATCTTCATCTCTGATTCCCCAGAGGACCCGTCTCTGACTACCAGACCTCAGCGCTCCCTGGGAAAGGCCCCCAGGGAG Homo sapiens hg19 +snp_rs10817727 snp_rs10817727 1 chr9 117979260 117979455 - TGTTTTCTCCTCTCACTATAAGGATGTGGCCCAACTTCCAAGGGTGCCCCACCATTGAGGTCTTCACTGCCAGGAACTGAAATCTCATGGGACACAAAACCCACCTACACATCCTCTCAACTTCTCCTTTCTGTGTTGAGTC Homo sapiens hg19 +snp_rs10440685 snp_rs10440685 1 chr5 77182925 77183128 - AGGGGTTAAGTCTTCGCATTGTGAGGTTCTATTGACTTTTCCTGCAGGCTTGCCCTTTATCCTTGTCTGTATTTTAGTTTTTAAGAAGCCTTCAAAAGGTAGGGCACTCATTAGTGGTTCCATAGTGGATGGTTATGTTCAGTTGTTAT Homo sapiens hg19 +snp_rs10486239 snp_rs10486239 1 chr7 8584076 8584285 - ATGACACCATCATCTGCCTCAGTACGGTCTACATTATAACATTGCACTGCACTCCTAACTTCACTATTCTTTTGTTTATGGCATATGCCTATGATGTCTTCGGGTAGGGATCATTTCAAATGCCAAGCATCCTTCCATGTAAACATTCTTTAT Homo sapiens hg19 +snp_rs10505770 snp_rs10505770 1 chr12 13025899 13026105 - GAGTCAGTGTGAGCTGTATGGTGTCTACTCTTCCCTCTGTGGTTCTTCAAAGGGAGTAGAGGGTGGGTGATGGGGGTGACTCAAGAATGCATAGGACTTTATCAATCAAATTCCCATACGGAATCAGAACAAGCCTGGCAGGTTCATGGACCA Homo sapiens hg19 +snp_rs10223664 snp_rs10223664 1 chr6 98677548 98677736 - ATTCCCATGACCTCAACCAACCTCCAGTCACCACTAATTTTCACATATATGTCTTTGGTTCTTATCATTCTCCTAAGATCTACACTTCTAATTACATTGAAAATAATTATATGTGCATATTCTATATGTTCTATAA Homo sapiens hg19 +snp_rs10490026 snp_rs10490026 1 chr2 210733280 210733489 - GGTTGTCCAGTTGAAACTACAAAAAGTCTAATGAATGTCATTGCACAGCATGGGAGTCTCTTACAGTCTACAGGTAGAAAACATCAGGAGTCTGGCTACTTTCCTTGACTTCTTTGCCATTTTTTCCTTGAATTTTATAAGATCATTATGTATAT Homo sapiens hg19 +snp_rs10514527 snp_rs10514527 1 chr16 82137489 82137696 - TCGTCAGTGAAAATTTCTTGCCTGAACATTTAAGCCTTACCAAAAAACCCTACCCAGGCCAAGAACAGCATGTTTCTATTTAGAACCTTCTCTATGTGGAATTAGTTCACCTCTGACAGTCAGGAGACAGAGCACAGGGCAATGCTAAAGAGAGG Homo sapiens hg19 +snp_rs10744146 snp_rs10744146 1 chr12 17212724 17212922 - CACTTCAGTGATTGCTCCTTTGTGTTCATTCAACTCATGCTGCATCAAAATACAGGCCTCTTGGCTCTAACGCATGGTTCTAGCTCTTTGGGTACTAATACTGACTTTCTTCTGCCTCAATTTGTCAATTATCATTCAAATTTGT Homo sapiens hg19 +snp_rs10845745 snp_rs10845745 1 chr12 13466200 13466390 - AATAAATGCATGTTGCAGGATAATACCACATGATTCAGGGACAAACTTCTCTCCTCCAGCTGCTCCTCTGACACAGTCTTAGACCTCTCTTATCATTGGTCTACCATTTATTTAGCAATTTTTATTGAAAGCCTTCTA Homo sapiens hg19 +snp_rs1032886 snp_rs1032886 1 chr12 44528902 44529101 - TTTTCTAGTAATTTATTCCTGCCATTGGGGTAAGCTTATGGAGACATATACAATGATGCCCAACTCTGCTATTGTTTCCTTTTCTGGTAATTTAGAACCAATACAAAAAGAGAGAAAGAAGGAAATATCTTTCCTGGAGGTTATAT Homo sapiens hg19 +snp_rs10487449 snp_rs10487449 1 chr7 126071915 126072127 - ATGAATTACAACCTGTTTCTAGAACAGTTATCAAATCTTCTTGGCTTTGGGAAATAGATTTAGGTTGGGGAATACTCTTTGGGTAAATTCAAGTTAGTGTCAACTTTTTATTTGACAGTTTTCATTTTTATTGATTTGTCCATAATATGAAGTTTGTAGT Homo sapiens hg19 +snp_rs10813205 snp_rs10813205 1 chr9 29943479 29943701 - CAAATTTCATATTGAAAGCAATGGTGATATTTTCTATCTTCTGGTTTTTGATGGATGTGTAAATTTCAAGACCTCCATCACGATTGCCAGGCAAGGCATATATATACTTAGGGCAATTCCATTTCCTAGATTTGGCAGGTTATTGAAAGGAATTTGTTGAGAAATTT Homo sapiens hg19 +snp_rs1003346 snp_rs1003346 1 chr9 111815176 111815380 - CCTGCCTTTACCCAGTTTCTCCTCTTTAAGCCTGACATATAAATTAAACCACTTTACTTTAAGGATTTAGTTAATATTCTAGAAATGTTTCTTCCTCTATTTTCTCCAGTTGATTCCCTTTCTTTTTTTCTTTCAAATAGGAAAGGTTACTT Homo sapiens hg19 +snp_rs11185125 snp_rs11185125 1 chr1 108061495 108061685 - AAATGTGTTAGGGAGGCTTCCAAGGTAAGGAAGCAGTAAATAAAGGCACAAAGATGGGAAAATGTGGAGCATATAGTAGAAATAAGAATTATATTAATAACAATTGTATGTTTAAAACAAGGTTCATGAAGGCATG Homo sapiens hg19 +snp_rs11073674 snp_rs11073674 1 chr15 87361824 87362022 - TATGCTGAGCCACGATGTTGTACTACTGGCCTGCAAGTATTTATTCCAGAAATGCATTTTCCCCTTTGTCAACTCCCACTATCACCATCCACTTTGGTCATTCACACCTTCTCTTTCCTGGACAAGTTTTCACCAAATCCATCTA Homo sapiens hg19 +snp_rs10187631 snp_rs10187631 1 chr2 120343679 120343887 - GGCAGGTTATTGGGTCCCCTTGCAGCAGCAGGAAGTCAAGTGCTTCCTTTCAAGTGACCCAGCCACTCCCTGCATTCCTGATATTTTTGCACCCCTCCCTTCTCGTTAAGCCACCAGCCAGCTTCATCTTTGACTCTGTACATCTCTTCTCTACCCC Homo sapiens hg19 +snp_rs11125812 snp_rs11125812 1 chr2 59989457 59989672 - GCACCATCCATGGTAATGGAGCAGAGAGGGATGCCCTGTGCTATTGGTAGAAAAGACAAAATGTGAAATAGAATGAAAATTGCCTCCAGTCACTTAATTTGGAGGCAGCACAGGAGCTGTGCAGCATTTCAGTCGGATGGTACCTTGAATTAAAAGAACTAA Homo sapiens hg19 +snp_rs10837327 snp_rs10837327 1 chr11 40082638 40082845 - TCTTCTAGAAAATTTTCCCACTATCAACAATAGTCCCAAATTGTCAGCATAATACTCCCACACTCTCACCATAACCTGTCTACTCAGTTTTGCTCTCATCAGATTGTAATCATATTTTTATGGTACATGTATCGTTTGTCTTGACCAACATATTATA Homo sapiens hg19 +snp_rs10937470 snp_rs10937470 1 chr3 191000655 191000854 - ACAAGTAAATGCCAAGATCGGAGGTCATTATACTATAACATCACTGGAGCCATAAAATTGAAATTGGAGATATACTGAAAGACTTTGACTTAAAAAGAAAACCAGCACAATTAAAGCAAGTATTAAAGAGAGTAACTGATGGGA Homo sapiens hg19 +snp_rs10510060 snp_rs10510060 1 chr10 121863321 121863513 - CAAGTTCCAGATGTAGCGAATCTCTGCCTGTGTGGACAAAGAGACACATTCAGAGGTGAGCCCAGAGGGGGTAAAGTGGACTGGGGAGAACTTCGGAGGATGTTCATGTCCAGGAGCAGCCCCACGCCCTGTATGGTCGG Homo sapiens hg19 +snp_rs10871565 snp_rs10871565 1 chr18 75698200 75698390 - AGAAGAGGGCTACTACAGCAGAATGGCAGAGAGATGCCTCTGCAGCAACAGAACGAATACTTGCTTTAAAAAAAATGTCAAAATGTGGATGTGCCTCCAATCATTTAAAAAATAGAAGGTGATAAGTTGAAAATGTC Homo sapiens hg19 +snp_rs10950049 snp_rs10950049 1 chr7 66230706 66230897 - CATAACCTCCCATGTTATCAGGAAACTGTCCTCTCAATCCACAAAGATAAGCTGGCAGCAGCTATATTTGTATAAGGTGAATGGTCCCCCAATTCAGGATCACAGCTGATTGCCTCCAACTGTGTTAGAGTCTTTTGCTT Homo sapiens hg19 +snp_rs10816943 snp_rs10816943 1 chr9 112983665 112983860 - GCAGTTGAGGACAAATTAAAACTTCCATGAGGCTCAACGTCCAGCAAACATCTAACTTAATTCCACTTCTCAAAGTTCCTTTAGTTCTTGGGCTTACCACATCTCCAAATCCACCAAAAGACAAACATAGCCAATTAGAATAT Homo sapiens hg19 +snp_rs10512393 snp_rs10512393 1 chr9 112153006 112153198 - TGTTTCTAATTCAATCGTCCACATGCCCCTGTACTGAGTGGCTTCCATTCAGGTGTTTGTTTTTGCCAGTGATGAAACTGTCTATTTCTCTCCATGTAATGAGTGTCATCCTGCCTTAAAAAAAAAATGAGAAAAATAA Homo sapiens hg19 +snp_rs10511942 snp_rs10511942 1 chr9 37702718 37702918 - CAACAAAGAATGACCTCGAAGACTCTACATCAAAAAGTATTGTGGGCCTAAAAGCTTCAGACATACAAAGAAACACAATCTAGAAAATACCCTTCCAGAGCACTGTGTAAGCTATGGTTTACCCTTCCTAAGTGAGAACTAGAATTA Homo sapiens hg19 +snp_rs10240790 snp_rs10240790 1 chr7 89880793 89880985 - GGGAATAACAATGTCCTCACCTCATGCAGCTATTGGTCTGGCATGGGATTTTATAGAAGGCTTTGTATGTAACACAAGGATCTTAAAAAGCCATTGAATGGTTTGAGACTGAACATATAAACAAAACTGGTCAGACTATAT Homo sapiens hg19 +snp_rs1147199 snp_rs1147199 1 chr9 87275738 87275942 - AATCCAAATAATGTTCATCATCAGACACTTCATTTTCCCAAGAATGTCTGTATTTTAGTGGAGGACACTGGGAAAAAGATGTAATCCAAAGGAATTTCAGGTACCATGGCAACCATAAAAGAGGGAGTATTTGAGCATGGAGGACTCAACAC Homo sapiens hg19 +snp_rs1058326 snp_rs1058326 1 chr9 27446918 27447133 - ACAAGCTTTTCCTTCAACGAACCTTTGTAGGCATAAGGACGTGTGTTATCTGCAAAGGTCTCTGCAGACAGGACCTTTGGGTGTTATATCTTAAAAAAAAAATTCATGCTAATTTCCTATTCTAGTGAATAATTCTGTCCATATTTTCTTTCACATAATCAT Homo sapiens hg19 +snp_rs10484820 snp_rs10484820 1 chr6 139858111 139858344 - GCGGATAGAGTTTTGGTTTGAACATGCGACTACCCTGATTCCACATTCAGGCGTTTTGTCATGAATTCACCGAGGGACTGTTGGTCCAGGCCTCTGTAGGCAAATTATATTTGCCAATAGATGACATTTATAGTGTAACTGGATATCCCTGGATGAGAAGCTAAAAATGAAAAAGTAAATA Homo sapiens hg19 +snp_rs10829531 snp_rs10829531 1 chr10 130761792 130761989 - AGAGAACTAGGGCAGGCAAGAGCAGCTCACACATGCCTTCCCCACCATTGCAGATGGGATGCATCTTCATGTCTCACTAAGATGCTGATTAGTTTTCAAGGTTAATAAAATTATGGGTTTTGAGTCTGAAATCTTCATGTACAGT Homo sapiens hg19 +snp_rs10835211 snp_rs10835211 1 chr11 27701208 27701403 - TCAACTGAGCGACCAGAGCTCTGCTGGTGAAACAGGAACTTGTATTGTGCCCCTGACGTGCACCTTGAAGGTGTCAGCTCATTGTCCCTTTGTTCACATAAATAGTTTTTTAAGAATTGTTTTTGATCTTGTGAGCCTCTAA Homo sapiens hg19 +snp_rs10160742 snp_rs10160742 1 chr11 115239233 115239435 - TGTTAACCCAAAGATGGATAGGAAAACAAAAATATGCTACAAGGAAAATTATTATGGGCTATTCAGGTGTTCTTGTTACTGTATGTGCCCCTAATATTAGGATTTTCTTCACAGAACATTATCATTCAAAAAAGAAGTCATTACATATA Homo sapiens hg19 +snp_rs10512461 snp_rs10512461 1 chr17 32475233 32475435 - ATCTTCCAGTTTAGAACTTTAAGCTGTAAGCTCTCTGGAAGTCGTGCTTTCAGGGGTATATAAAATTCTTTCTGATGTGATGAAGGGGTAAGACAATGACTGAGAGCTGACTATTTTGATGACCCACAATGTCTACTTGCAAAGAAAAA Homo sapiens hg19 +snp_rs10869031 snp_rs10869031 1 chr9 74130136 74130327 - TGTCCAGTCATTAGACCAGCCCACTCTTTCTCACTCCCTGTAGTCCTAAAAACAGTTCTTAAATATCCTTCTGTTTGAAAAATTCCCATCTGCTCCACCCACGATCACAGCAGAATGAAGACATCGCGTTCCTCTGTT Homo sapiens hg19 +snp_rs1055010 snp_rs1055010 1 chr7 29550950 29551166 - AGGCACTATGCCTGACTAAACAAGATGGCTGGCAAACCCACTATGATAAAGATACAGTATTATTGGCATTTAAGGTTCAGCTGAAAGGTGTCAGCATTTTTCTGGTAGTGGTACTTTGCCTTCCAAACTGTAACAACTGGATATTGATCACAATAAGTATTTTA Homo sapiens hg19 +snp_rs10930486 snp_rs10930486 1 chr2 172472416 172472622 - CCCTCTTCATTGAAAGAAAGCTACTACACCGATCCCTTGGGTTGTTTTGTGTGCGTGCATGTGTGTGTTTATCTTTAAATATTTAGGGAGTACAAGTGCAGATGTCTCACATGCATCTATCGTGTCATGGTGAAGTCTTGGCTTTTAGTGTAT Homo sapiens hg19 +snp_rs1052448 snp_rs1052448 1 chr9 18927860 18928079 - CTGATTTTGAAAAATAGTAATTTAGAAATTACACAGTACTTTTAAAAGCAGACAACTGAGAATTATTTGTTGGACAAAAAAGAATTCCCTAAAATGACAAAAAACAAAAAACAAAAAACCTTCACCACTTCCAGAGCACTTGAATAAAATGAGAATCACTTGACTCA Homo sapiens hg19 +snp_rs10488735 snp_rs10488735 1 chr11 34438404 34438596 - TCTGGCATTAAGGTTCTCTCTATCCAGTGATGCAATAGACAGTTGCTGGTTTTGCAACTCTATGCACTCTACATTTTGTAATATCATCCTAATTTTGCTTTGTAGAGTTATTCCCTCCTCTACTCTACCTTTTATTTACA Homo sapiens hg19 +snp_rs10255854 snp_rs10255854 1 chr7 38959675 38959892 - GAGTTTCTCCAGTAATTTCCAGACGTTTATGTGTCAGAGAAGAAGTTCATGATACATCAGCTGGAGATGTTAGGCCTTGGGTTCTGGTACTGCCACATAAGTATTTTTCTCCAGCAGTTGTCAAACCAGTTAGAAATATTACCCAGGAGTCTAACAATGATGCTCT Homo sapiens hg19 +snp_rs10961084 snp_rs10961084 1 chr9 13484879 13485076 - AGCGTGTTGGTAGAGCCTATGTGGTTGATGCTATTTCACAGGACTTAGTTATAGAAGAGGAAGGTTTACCTTCATTTTAAATTAATGCAAATGGTGCAGATTCAGCCCCAGTCAACTGGTATTTTCCAGATTCATAGTTTACTTT Homo sapiens hg19 +snp_rs10189774 snp_rs10189774 1 chr2 171375347 171375538 - AAACAGGGAATAATTCCAGGAGTAACCTATTTCCACATTTTGATTGAGGACAGTTTATTGATGAGTTTCTCAACAATGAGGGTAACAAATACAATTCTTTCTTCCAGTGACCATGGCTAATCAATCACGGCCTTCTTT Homo sapiens hg19 +snp_rs10893306 snp_rs10893306 1 chr11 124813366 124813553 - AGGGATGGTGTCGTCTATTACTTTTGAATGTGCCGCCTTCCTCCTCTTCCACATCCCACCACTTTTATTAATGTTTGGAACATAGAGTGTTCTTCACACAGTAGGCAATTATCAGATGCTGGCCAGCTGATTCCC Homo sapiens hg19 +snp_rs1106944 snp_rs1106944 1 chr11 126008119 126008321 - CATGTTATAAAACCATAGGCAAACCAAAGTCACGAAGAGAGAAAGGCTGAGCCAAGAGACCACAGCCCAGGAGGAGAGAGAATGACGAGGCCGGGTACTTTGCTTAATTAAAGTCTCATATCCCTCATAGTTATCTCTACATCCACTTT Homo sapiens hg19 +snp_rs1055352 snp_rs1055352 1 chr9 128910268 128910455 - ATGGTGTAAAAACACAGATTTGTCCCACCTGGTTTCACCCCACTTTCCTCTCTGGTCCCAGGCCTCAGGGTCTGGACATTTCTGCCAGGGAACATCTGTTCTGCAGAGCAGCCAGGACTCCCCCTGCCACCCCCCA Homo sapiens hg19 +snp_rs10141526 snp_rs10141526 1 chr14 62303100 62303301 - GGAAAATGAGGGACTGGGGAAGGAATGTAGGAGAATGGCTACAGGATTTCAGAAGGTGCACATTTAATATTCAATTTTAGACTGTTTATGTTACCAAGATATAAACTTCTCCTATCCCTCCAAACCATCAATTGGTTTTCTACATATT Homo sapiens hg19 +snp_rs10094093 snp_rs10094093 1 chr8 4505761 4505952 - GCACCATTAGGGGCCACTTGGTGACAGACAATCCCGTAGATCACAGAGAATGTGGATCATGTCATTATATCCTAAGTGACTCACAGGTGGGGAAGCAGGAACAAGATAAACAAAAAACTACAAGAAATTAGCAAGAAAAA Homo sapiens hg19 +snp_rs11009888 snp_rs11009888 1 chr10 35007947 35008138 - GCTTTTTTCAGACAGGTCTAAAAAGGGCTCTGCCCTAGTCTATCCCTAGCAGAGATGTTACATGTGCCTGGCTCAATTCAACGTATCAGTATATTGTGGGGAGAAAGGATGAATAAGGACAACACCACAAGTTGTGAT Homo sapiens hg19 +snp_rs11082351 snp_rs11082351 1 chr18 41484188 41484382 - GGGAATCCCAATAGAAGAAGGTAAAGGTGATGCTGTTCTCAACCAAATTAAAACTTCAATGCTTCTCTGAAGTAGGAAAAAGGCCTTCTAGAGTATGTAATCTTTTAAAACTTTTTGAACATCAAAGAGGTCTCAGAAAAT Homo sapiens hg19 +snp_rs1113272 snp_rs1113272 1 chr4 165646618 165646832 - GATTCAAATAGTTCTTTCTTCTCTGTAGCCTTGACTTCAGGTTTGACTGGCTCAGGTGACGTCTCACTATTCTGTTTAGTGAATAGTGTTGTCCAGCCTGTTGTCCAGCCTGCAATGCATACATCTCACTATTCTGTTTAGTGAATAGTGTTGTCCAGCCTG Homo sapiens hg19 +snp_rs10250461 snp_rs10250461 1 chr7 22289201 22289407 - GGTGTTTTATAAACGGTGTTTGGTGGTCTAAGAAACCAGTCACCATAGAATAAAACATATATGTTATAGTTCTGCGACTACCTTATTTATTGGAGAATTGCCTAACTTTCTGTGTTTCTCTACCAGTGAAAGCTTTATAAAAGGAGAATTATT Homo sapiens hg19 +snp_rs11143230 snp_rs11143230 1 chr9 74887553 74887757 - TAGATTTCCAAGCCTTGACTCTTAACATCTGTCATGGAACCATTATAGCACCATCTGCCCAATTTCCCCGCTGATGATTTCACCTGACTATGTAATCCTGGAAGAGGGGTGATGCCCATTAACTTGTAGTTGGTTTATATAAGCTAGAGCA Homo sapiens hg19 +snp_rs10520689 snp_rs10520689 1 chr15 90950208 90950408 - GGGAGTGGTTCCTCAGCTTCTACGTTGAAAAGGATTCTGATCTATCAGCAGTGCTTGCTGTGGGTGTAAAATAACCTACCACAAATCTAACATCCTTGCTCTAGACTACGAGATCCATCTTAAAGTATGGCCTCCAGAACTAAACAC Homo sapiens hg19 +snp_rs11079784 snp_rs11079784 1 chr17 45702116 45702318 - GCTATTTGAAAAACAAAACATCTGACACAGAAAAGGCTGAATTAAAACCTTTAGAGACCCAAAGCAGCAGGGCTATTGTGCCCAAATCACTCAAGGTATTGGTAGGAAAGAACACAAACTGAGGAAGGTTTAATAAAGGACTATTTACAG Homo sapiens hg19 +snp_rs11632663 snp_rs11632663 1 chr15 27564636 27564822 - TGGACACCCTCTTATCCAGCCTCGTCCAGTCCTCTCCATCCTCCTGTCTGCCATCTTCCCGTGGCATTGGCATATTTGCCAACAGCCTGCCCCTCCTCATGGTATTACTCACTATTTTTTCTCCTTATGTTAACA Homo sapiens hg19 +snp_rs10079889 snp_rs10079889 1 chr5 32975335 32975532 - AAAATCTAGAATACTTTACCTTGCGTTTTAGATACATGTAGACACATCTTATCCTACTCAACAAACCCTGCTCCATCCCCAAAATGCTCCCACTTCGCTGTAAATTTTTAAAGTACTGGGATTTTTTTCTGCTTATCTTTGCAT Homo sapiens hg19 +snp_rs10504373 snp_rs10504373 1 chr8 65107774 65107977 - AGTTCTCTTTAGGGCAATCATTGTAGTACCTTCCACATTTCTATTGCACTTAAACATAAGTTCTTGATGTGCTCTACAGCTCTGGATCACAATTTAAACATAATATTTACTCTATCTCAGATACGGCCTCTTTAAAACCACAACTTTT Homo sapiens hg19 +snp_rs1160382 snp_rs1160382 1 chr7 149279842 149280037 - TTGTGAACATTTGTAGAGCTGTGAAGATGGAAATCTCTTAGCACTGGAAGTCCTTAGCATTGGAAGCACATTGTCATGGTGTTTGACATTCCTGGGGACAAAAGGAGAAGGTGGTGAGGAAAATAGGATTGTTATTCTGTCGT Homo sapiens hg19 +snp_rs10887788 snp_rs10887788 1 chr10 89898602 89898802 - ACTAACAAAAGACAAACAGGGCAGTCTCCATGAAGATGTCTGGGCATGCAAATAATTCTGGTTTTGATGTAATTATCAGACTCCTAGCACTGAAGGAGAGATGGTTGGAGAATTCTATAGTACTTCCAGCTTATCTGCATAGTTTAT Homo sapiens hg19 +snp_rs10257539 snp_rs10257539 1 chr7 135439746 135439954 - GATCTTAGGTGTCTTGTTAGCTAAGGGAGAAAACCCAGAAGAGTTCTGTCACTGTGTCCGTATGTCCCTCCAATGATGGGAATACCCCAATCCACAAGTGACTCTTCTCTCCAAAAAGAATTTCTGCCATCTGCCATCCCCACAGCTGCAGGCCAC Homo sapiens hg19 +snp_rs11002633 snp_rs11002633 1 chr10 80447619 80447825 - CACTATTGCTTGCATGGGCTGACACTTGTGAAGTGATATCAGAAATATTGTTAGTGACATTTTTATTTGGAATTTTAAAAGAAGAAATTGACATCTCCTTCCTTAAAAGGCTACAAGAGTATCTTCAACCCTGACATCTTAAATGTTTATTTTT Homo sapiens hg19 +snp_rs1058932 snp_rs1058932 1 chr10 96796712 96796899 - CATCTGGCTGCCGATCTGCTATCACCTGCAACTCTTTTTTTATCAAGGACATTCCCACTATTATGTCTTCTCTGACCTCTCATCAAATCTTCCCATTCACTCAATATCCCATAAGCATCCAAACTCCATTAAGGA Homo sapiens hg19 +snp_rs11063356 snp_rs11063356 1 chr12 4938444 4938642 - CCTCTATATTTAGCGAGCAATAAGAGCAATGTGGACACGTTATGCCAGTGAAAAGTTTGTCGATTAGCTCCTTTTCTACTGGATAATCATATCCAGCAATGCTTCTGGACAGCACAGGCAAATCAGCTCAAGGAGGGGAAGCACCCTC Homo sapiens hg19 +snp_rs1016726 snp_rs1016726 1 chr7 29356254 29356442 - AGACTCCATACTCTAGAAAGCTTAGCTATTTCTTTGGCAAATTAGAAGTATAATCCCAACATTGTGGAAAAAAAAAAATCACACATCTTTGTATGAATTCAGTAAATGTTGATGTCACATTGGGGGCAGCAGCTCT Homo sapiens hg19 +snp_rs10875815 snp_rs10875815 1 chr12 48834175 48834367 - GACCATGAGAGAGCTAATGGCAGAGGAAGGACTGGGCAGAGCCTGTGGCAAACTTCAAAAAGAAACCAGAAACATTTAACAAAGACCCTTTAGATGATGAAACACAATTGGAGGATTAATGAGAACTATATTTGAGGGA Homo sapiens hg19 +snp_rs10957982 snp_rs10957982 1 chr8 81455607 81455809 - ACTGGTTTAGAGTAATTCAATTTAGCTGTCATTTAATCCAGACCAAAAAAAGCCATTCACCTTGTTTAGCTGCCGCAACTGACTCATGTGTCAAGGAACTCAGAAATCCAACTTAGAGATCACAGGTCAACCTGTGCAAAGCTTGCGGC Homo sapiens hg19 +snp_rs1258540 snp_rs1258540 1 chr7 63109119 63109314 - GGGACTCTCCTTCAGCATCAAGCTGCCACCCTCAGATGTGGTCCCCTGCACCTCCCTCCACAGGCTGGCCCCTGCCTGCCTCCTCACCTCACATCTCCCCAGTCACCTCCTCTGCTCCAAGGCATGGCAGGTTCCTGCCCTTCT Homo sapiens hg19 +snp_rs10087078 snp_rs10087078 1 chr8 8930587 8930780 - TAAGATACTGCCTTCTGCAAAGATAAATAATGTTGATTCACTGCGCTTCCAAAATCAAGGACAAAGCCGAAGGCATGAGGCCAGGTGATAAAGTTTATGGCTGAGAAGGCAACCAAGATTCAAACTGACTGACAGCAGAA Homo sapiens hg19 +snp_rs1050190 snp_rs1050190 1 chr3 141644656 141644852 - ATAAAAAGAGGACAAGACCCCCATCCTACATGTTTGGAATCAGGTGTTCACCGGTCCCTATCTGGCGACTGTACACTGGTTCAAAGGGCAGCAGAGGCAACAGGCAGTTACTTCAGAGGACACTGAACACTATGATCTGGAA Homo sapiens hg19
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/canonicals.tsv Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,48 @@ +RB1 NM_000321 +KIT NM_000222 NM_001093772 +FGFR3 NM_000142 NM_022965 NM_001163213 +GNAS NM_000516 NM_016592 NM_080425 NM_080426 NM_001077488 NM_001077489 NM_001077490 NR_003259 +NRAS NM_002524 +ERBB4 NM_005235 NM_001042599 +CDKN2A NM_000077 NM_058195 NM_058197 NM_001195132 +CDH1 NM_004360 +KRAS NM_033360 NM_004985 +VHL NM_000551 NM_198156 +CTNNB1 NM_001904 NM_001098209 NM_001098210 +BRAF NM_004333 +EGFR NM_005228 NM_201282 NM_201283 NM_201284 +AKT1 NM_005163 NM_001014431 NM_001014432 +JAK2 NM_004972 +NOTCH1 NM_017617 +SMARCB1 NM_003073 NM_001007468 +PDGFRA NM_006206 +SMO NM_005631 +SRC NM_005417 NM_198291 +FBXW7 NM_018315 NM_033632 NM_001013415 NM_001257069 +FGFR1 NM_015850 NM_023105 NM_023106 NM_023110 NM_001174063 NM_001174064 NM_001174065 NM_001174066 NM_001174067 +MET NM_000245 NM_001127500 +MPL NM_005373 +GNAQ NM_002072 +GNA11 NM_002067 +CSF1R NM_005211 +MLH1 NM_000249 NM_001167617 NM_001167618 NM_001167619 +KDR NM_002253 +ABL1 NM_005157 NM_007313 +PIK3CA NM_006218 +HRAS NM_005343 NM_176795 NM_001130442 +FLT3 NM_004119 +ALK NM_004304 +TP53 NM_000546 NM_001126112 NM_001126113 NM_001126114 NM_001126115 NM_001126116 NM_001126117 NM_001126118 +PTEN NM_000314 +JAK3 NM_000215 +IDH1 NM_005896 +PTPN11 NM_002834 +RET NM_020630 NM_020975 +ATM NM_000051 +HNF1A NM_000545 +FGFR2 NM_000141 NM_022970 NM_001144913 NM_001144914 NM_001144915 NM_001144916 NM_001144917 NM_001144918 NM_001144919 +APC NM_000038 NM_001127510 NM_001127511 +ERBB2 NM_004448 NM_001005862 +SMAD4 NM_005359 +STK11 NM_000455 +NPM1 NM_002520 NM_199185 NM_001037738
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/tobed.pl Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,37 @@ +#!/usr/bin/perl -w +# + +my $mani = shift || "TruSeq_Amplicon_Cancer_Panel_Manifest_AFP1_PN15032433.txt"; +open M, "<$mani"; + +my %probes = (); +while (<M>) { + if (/\[Probes\]/) { readline(M); last; } +} + +while (<M>) { + if (/\[Targets\]/) { + readline(M); + last; + } + my @row = split(/\t/, $_); + $probes{$row[2]} = [@row]; + #print STDERR join(":", @row[2, 9, 11]) . "\n"; sleep 1; + +} + +while (<M>) { + my @row = split(/\t/, $_); + #print join("\t", @row[3, 4,5]) . "\n"; + my $ori = $probes{$row[0]}->[13]; + my $oriT = $row[6]; + my $s = $row[4] + length($probes{$row[0]}->[9]); + my $e = $row[5] - length($probes{$row[1]}->[11]); + if ($oriT eq "+") { + $s = $row[4] + length($probes{$row[1]}->[11]); + $e = $row[5] - length($probes{$row[0]}->[9]); + } + $row[4]--; + $s--; + print join("\t", @row[3, 4, 5], $row[0], 100, $oriT, $s, $e) . "\n"; +}
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/TSACP/truseq_amplicon_cancer_panel_manifest_afp1_pn15032433_b.txt Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,449 @@ +[Header] +Customer Name "ILLUMINA, INC." +Product Type 15032433 +Date Manufactured 25/10/2012 +Lot 35105 +DesignStudio ID NA +Target Plexity 212 + +[Probes] +Target Region Name Target Region ID Target ID Species Build ID Chromosome Start Position End Position Submitted Target Region Strand ULSO Sequence ULSO Genomic Hits DLSO Sequence DLSO Genomic Hits Probe Strand Designer Design Score Expected Amplifed Region Size SNP Masking Labels +MPL1_2 MPL1_2.chr1.43815008.43815009 MPL1_2.chr1.43815008.43815009_tile_1 Homo sapiens hg19 chr1 43815008 43815009 - AAGTGGCGAAGCCGTAGGTGCGCACG 0 TCAGCAGCAGCAGGCCCAGGACGG 0 - ILLUMINA NA 183 TRUE +NRAS1_7 NRAS1_7.chr1.115256528.115256531 NRAS1_7.chr1.115256528.115256531_tile_1 Homo sapiens hg19 chr1 115256528 115256531 - CAATAGCATTGCATTCCCTGTGGTTTT 0 AGAGTACAGTGCCATGAGAGACCAAT 0 - ILLUMINA NA 182 TRUE +NRAS8_13 NRAS8_13.chr1.115258730.115258748 NRAS8_13.chr1.115258730.115258748_tile_1 Homo sapiens hg19 chr1 115258730 115258748 - GGGTTTTCATTTCCATTGATTATAGAAAG 0 CTGACAATCCAGCTAATCCAGAACCA 0 - ILLUMINA NA 184 TRUE +ALK1 ALK1.chr2.29432664.29432664 ALK1.chr2.29432664.29432664_tile_1 Homo sapiens hg19 chr2 29432664 29432664 - GATAAAATCCTAGTGATGGCCGTTGTA 0 GACATCTACAGGTGAGTAAAGACTGCC 0 - ILLUMINA NA 188 TRUE +ALK2 ALK2.chr2.29443695.29443695 ALK2.chr2.29443695.29443695_tile_1 Homo sapiens hg19 chr2 29443695 29443695 - TGCTGCCCATGTTTACAGAATGCCTT 0 CACCAGAACATTGTTCGCTGCATTG 0 - ILLUMINA NA 171 TRUE +IDH1_1_2 IDH1_1_2.chr2.209113112.209113113 IDH1_1_2.chr2.209113112.209113113_tile_1 Homo sapiens hg19 chr2 209113112 209113113 - GAGGGTTGAGGAGTTCAAGTTGAAACA 0 CATGCTTATGGGGATCAAGTAAGTCAT 0 - ILLUMINA NA 182 TRUE +ERBB4_1_2 ERBB4_1_2.chr2.212288942.212288955 ERBB4_1_2.chr2.212288942.212288955_tile_1 Homo sapiens hg19 chr2 212288942 212288955 - ACTACTGGTATAGTGCTGGTTTGTTCA 0 AGAACGTTTGCCTCAGCCTCCCATCTG 0 - ILLUMINA NA 190 TRUE +ERBB4_3_4 ERBB4_3_4.chr2.212530066.212530135 ERBB4_3_4.chr2.212530066.212530135_tile_1 Homo sapiens hg19 chr2 212530066 212530135 - CATTTCAGGGTCCTGACAACTGTACAA 0 AACTGCACCCAAGGGTAAGCATTCTT 0 - ILLUMINA NA 176 TRUE +ERBB4_5 ERBB4_5.chr2.212576857.212576857 ERBB4_5.chr2.212576857.212576857_tile_1 Homo sapiens hg19 chr2 212576857 212576857 - ATACTCTGCTATTTTATAATGAAGATGCAA 0 CCAGTAACATTGACAAATTCATAAACTGTA 0 - ILLUMINA NA 171 TRUE +ERBB4_6_7 ERBB4_6_7.chr2.212578341.212578349 ERBB4_6_7.chr2.212578341.212578349_tile_1 Homo sapiens hg19 chr2 212578341 212578349 - AGGGTAAGATACATAAACACTATCAATGA 0 TGCCTGCCCTAGTTCCAAGATGGAA 0 - ILLUMINA NA 186 TRUE +ERBB4_8 ERBB4_8.chr2.212587147.212587147 ERBB4_8.chr2.212587147.212587147_tile_1 Homo sapiens hg19 chr2 212587147 212587147 - TGAAAGTAATATTTGCTGTGTTGCAGG 0 CATTCTGTGTCAAGAAATGTCCACGTA 0 - ILLUMINA NA 172 TRUE +ERBB4_9 ERBB4_9.chr2.212589811.212589811 ERBB4_9.chr2.212589811.212589811_tile_1 Homo sapiens hg19 chr2 212589811 212589811 - GCAGACTTTGATCATGGTCCTATCTCT 0 GACTGCTTTGTATGTCTGTGATTTCTC 0 - ILLUMINA NA 176 TRUE +ERBB4_10 ERBB4_10.chr2.212652764.212652764 ERBB4_10.chr2.212652764.212652764_tile_1 Homo sapiens hg19 chr2 212652764 212652764 - AATGGTGGAGTCTATGTAGACCAGAAC 0 TCTTTTTAATTTCTCAAAATGTTCTACCCT 0 - ILLUMINA NA 172 TRUE +ERBB4_11 ERBB4_11.chr2.212812157.212812157 ERBB4_11.chr2.212812157.212812157_tile_1 Homo sapiens hg19 chr2 212812157 212812157 - GTGGCTCTTAATCAGTTTCGTTACCTG 0 GGTAAGGAATATATCCAAAATGGCAAATA 0 - ILLUMINA NA 186 TRUE +VHL1_2 VHL1_2.chr3.10183797.10183817 VHL1_2.chr3.10183797.10183817_tile_1 Homo sapiens hg19 chr3 10183797 10183817 - AAAATGGACCCCGGGGCGGTAGAGGG 0 ATACGGGCAGCACGACGCGCGGACT 0 - ILLUMINA NA 185 TRUE +VHL3_5 VHL3_5.chr3.10188245.10188301 VHL3_5.chr3.10188245.10188301_tile_1 Homo sapiens hg19 chr3 10188245 10188301 - GAACTGGGCTTAATTTTTCAAGTGGTC 0 AGAAGCCCATCGTGTGTCCCTGCATCT 0 - ILLUMINA NA 186 TRUE +VHL6_8 VHL6_8.chr3.10191480.10191506 VHL6_8.chr3.10191480.10191506_tile_1 Homo sapiens hg19 chr3 10191480 10191506 - TTGATGTGCAATGCGCTCCTGTGTCAG 0 GTATACACTGGAAGGGCAAAAACCAAAT 0 - ILLUMINA NA 186 TRUE +MLH1 MLH1.chr3.37067240.37067240 MLH1.chr3.37067240.37067240_tile_1 Homo sapiens hg19 chr3 37067240 37067240 - TGGGAGTTCAAGCATCTCCTCATCTTG 0 ATCTGGTGGGCATAGACCTTATCACT 0 - ILLUMINA NA 184 TRUE +CTNNB1_1_16 CTNNB1_1_16.chr3.41266040.41266137 CTNNB1_1_16.chr3.41266040.41266137_tile_1 Homo sapiens hg19 chr3 41266040 41266137 - GGTATCCACATCCTCTTCCTCAGGATT 0 GTCCAACTCCATCAAATCAGCTATAAA 0 - ILLUMINA NA 172 TRUE +PIK3CA1 PIK3CA1.chr3.178916876.178916876 PIK3CA1.chr3.178916876.178916876_tile_1 Homo sapiens hg19 chr3 178916876 178916876 - AGGGACAACAGTTAAGCTTTATGGTTA 0 AAAAATTCTTCCCTTTCTGCTTCTTG 0 - ILLUMINA NA 190 TRUE +PIK3CA2 PIK3CA2.chr3.178921553.178921553 PIK3CA2.chr3.178921553.178921553_tile_1 Homo sapiens hg19 chr3 178921553 178921553 - ACATTCGGAGATTTGGATGTTCTCCTA 0 TCACGTAGGTTGCACAAAGAATTTTTA 0 - ILLUMINA NA 186 TRUE +PIK3CA3 PIK3CA3.chr3.178927980.178927980 PIK3CA3.chr3.178927980.178927980_tile_1 Homo sapiens hg19 chr3 178927980 178927980 - CTTCTAATCCATGAGGTACTGGCCAAA 0 AACACATTTCAAAACACTTTTCTTCCC 0 - ILLUMINA NA 178 TRUE +PIK3CA4_11 PIK3CA4_11.chr3.178936074.178936095 PIK3CA4_11.chr3.178936074.178936095_tile_1 Homo sapiens hg19 chr3 178936074 178936095 - GGTATGGTAAAAACATGCTGAGATCAG 0 CTCGTGTAGAAATTGCTTTGAGCTGTT 0 - ILLUMINA NA 172 TRUE +PIK3CA12 PIK3CA12.chr3.178938860.178938860 PIK3CA12.chr3.178938860.178938860_tile_1 Homo sapiens hg19 chr3 178938860 178938860 - TAAACAACTCTGCCCCACTGCAGTGAA 0 CTTCAAATACATCCCACATGCACGACA 0 - ILLUMINA NA 174 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_1 Homo sapiens hg19 chr3 178952007 178952150 - CCAAAGCCTCTTGCTCAGTTTTATCTAA 0 AGCCTTGTAACACATCTCCTGAAACC 0 - ILLUMINA NA 175 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_2 Homo sapiens hg19 chr3 178952007 178952150 + CATTGCATACATTCGAAAGACCCTAGC 0 AGATAACTGAGAAAATGAAAGCTCACTCTG 0 + ILLUMINA NA 187 TRUE +FGFR3_1_2 FGFR3_1_2.chr4.1803564.1803568 FGFR3_1_2.chr4.1803564.1803568_tile_1 Homo sapiens hg19 chr4 1803564 1803568 - TTGCTGCCATTCACCTCCACGTGCTTG 0 TCTGTGGGGGCAGATGACGCTCAGG 0 - ILLUMINA NA 176 TRUE +FGFR3_3_4 FGFR3_3_4.chr4.1806119.1806153 FGFR3_3_4.chr4.1806119.1806153_tile_1 Homo sapiens hg19 chr4 1806119 1806153 - GCTCAGAACCTGGTATCTACTTTCTGT 0 TAGCTGAGGATGCCTGCATACACACTG 0 - ILLUMINA NA 188 TRUE +FGFR3_5_7 FGFR3_5_7.chr4.1807862.1807890 FGFR3_5_7.chr4.1807862.1807890_tile_1 Homo sapiens hg19 chr4 1807862 1807890 - AAACAAGGCCTCAGGCGCCATCCACT 0 GCCAGCCCGAAGTCTGCGATCT 0 - ILLUMINA NA 191 TRUE +FGFR3_8 FGFR3_8.chr4.1808331.1808331 FGFR3_8.chr4.1808331.1808331_tile_1 Homo sapiens hg19 chr4 1808331 1808331 - CCGGAGGGACCCCCACCCCTGA 0 CCCCCAGCGTGAAGATCTCCCA 0 - ILLUMINA NA 171 TRUE +FGFR3_9 FGFR3_9.chr4.1808949.1808949 FGFR3_9.chr4.1808949.1808949_tile_1 Homo sapiens hg19 chr4 1808949 1808949 - AAGCTCTGTGTAGCTGTCTCTCCATCT 0 TCGTGGGCAAACACGGAGTCGTC 0 - ILLUMINA NA 186 TRUE +PDGFRA1_4 PDGFRA1_4.chr4.55141013.55141049 PDGFRA1_4.chr4.55141013.55141049_tile_1 Homo sapiens hg19 chr4 55141013 55141049 - TACCCCATGGAACTTACCAAGCACTAG 0 CTATAAATGACCAGGACAGGTAACTGG 0 - ILLUMINA NA 178 TRUE +PDGFRA5 PDGFRA5.chr4.55144146.55144146 PDGFRA5.chr4.55144146.55144146_tile_1 Homo sapiens hg19 chr4 55144146 55144146 - GTCAGCTCCATTCAAGGGACTTCTATT 0 TACAATGTTCAAATGTGGCCCCAGGT 0 - ILLUMINA NA 188 TRUE +PDGFRA6 PDGFRA6.chr4.55144547.55144547 PDGFRA6.chr4.55144547.55144547_tile_1 Homo sapiens hg19 chr4 55144547 55144547 - AACATCTCTCTTTGCACCCACCTCCGT 0 ATGATGTAAATGGGGCCTATGGGGAC 0 - ILLUMINA NA 186 TRUE +PDGFRA7_23 PDGFRA7_23.chr4.55152040.55152109 PDGFRA7_23.chr4.55152040.55152109_tile_1 Homo sapiens hg19 chr4 55152040 55152109 - AGAGATTAAAGTGAAGGAGGATGAGCC 0 TTGCGAGCAGCCAGATCACGGTGGA 0 - ILLUMINA NA 174 TRUE +KIT1 KIT1.chr4.55561764.55561764 KIT1.chr4.55561764.55561764_tile_1 Homo sapiens hg19 chr4 55561764 55561764 - GTGTTTGTTGGTGCACGTGTATTTGC 0 CCCACGCGGACTATTAAGTCTGATTTT 0 - ILLUMINA NA 179 TRUE +KIT2 KIT2.chr4.55592185.55592186 KIT2.chr4.55592185.55592186_tile_1 Homo sapiens hg19 chr4 55592185 55592186 - CAGTATGGTGTGATGCATGTATTACCA 0 CAGAAGTCTTGCCCACATCGTTGTAA 0 - ILLUMINA NA 188 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_1 Homo sapiens hg19 chr4 55593464 55593689 - GAGAGAACAAATAAATGGTTACCTGTAAA 0 GTGGAATCACAAACTTTGGCAGGA 0 - ILLUMINA NA 172 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_2 Homo sapiens hg19 chr4 55593464 55593689 + CGTAGCTGGCATGATGTGCATTATTG 0 ACCCATGTATGAAGTACAGTGGAAGG 0 + ILLUMINA NA 175 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_3 Homo sapiens hg19 chr4 55593464 55593689 - GTGACATGGAAAGCCCCTGTTTCATA 0 TCTGTGGGGAGAAAGGGAAAAATAGAT 0 - ILLUMINA NA 185 TRUE +KIT20_21 KIT20_21.chr4.55594221.55594258 KIT20_21.chr4.55594221.55594258_tile_1 Homo sapiens hg19 chr4 55594221 55594258 - GCAGTTTATAATCTAGCATTGCCAAAAT 0 AGTTCAGACATGAGGGCTTCCCGTTCT 0 - ILLUMINA NA 189 TRUE +KIT22 KIT22.chr4.55595519.55595519 KIT22.chr4.55595519.55595519_tile_1 Homo sapiens hg19 chr4 55595519 55595519 - ACTATTTATGTAAATCAGTCTTACCAGGA 0 TAATGACCAGGGTGGGCCCTAAAAGC 0 - ILLUMINA NA 184 TRUE +KIT23 KIT23.chr4.55597495.55597497 KIT23.chr4.55597495.55597497_tile_1 Homo sapiens hg19 chr4 55597495 55597497 - CCACATTAGCATGATATACATACTCTCT 0 CTGGGAGAGATGAAACAAGTCATGACT 0 - ILLUMINA NA 187 TRUE +KIT24_28 KIT24_28.chr4.55599320.55599348 KIT24_28.chr4.55599320.55599348_tile_1 Homo sapiens hg19 chr4 55599320 55599348 - TGTGTGATATCCCTAGACAGGATTTAC 0 GGCTAGACCAAAATCACAAATCTTTGT 0 - ILLUMINA NA 184 TRUE +KIT29 KIT29.chr4.55602694.55602694 KIT29.chr4.55602694.55602694_tile_1 Homo sapiens hg19 chr4 55602694 55602694 - GAAGCAGGACACCAATGAAACTTCAAG 0 TGCCATCCACTTCACAGGTAGTCGA 0 - ILLUMINA NA 186 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_1 Homo sapiens hg19 chr4 55946114 55946257 - ATTCTCCAGCCTGACTCGGGGACCACACTG 0 CATTTGATTTTCATTTCGACAACAGAAAAA 0 - ILLUMINA NA 173 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_2 Homo sapiens hg19 chr4 55946114 55946257 + ATGCTTCCTTTTAAACAGGAGGAGAGC 0 GGACTGGTAGCCGCTTGTCTGGTTTGA 0 + ILLUMINA NA 188 TRUE +KDR3 KDR3.chr4.55953807.55953807 KDR3.chr4.55953807.55953807_tile_1 Homo sapiens hg19 chr4 55953807 55953807 - CTGAAGCCATAACAACAGTCTTCTGTG 0 ATTCCATTATGACAACACAGCAGGAAT 0 - ILLUMINA NA 190 TRUE +KDR4 KDR4.chr4.55955111.55955127 KDR4.chr4.55955111.55955127_tile_1 Homo sapiens hg19 chr4 55955111 55955127 - TCCTTATTTAGCATCTCACCTCGTCAG 0 AGCCCAGTCAGAGACCCACGTTTT 0 - ILLUMINA NA 174 TRUE +KDR6 KDR6.chr4.55960989.55961023 KDR6.chr4.55960989.55961023_tile_1 Homo sapiens hg19 chr4 55960989 55961023 - TTTATAGACCAAAGGGGCACGATTCCG 0 TGTAGAAGAAGAGGAAGGTACTGGCTA 0 - ILLUMINA NA 172 TRUE +KDR8 KDR8.chr4.55962507.55962507 KDR8.chr4.55962507.55962507_tile_1 Homo sapiens hg19 chr4 55962507 55962507 - GGAAATGCATGTGGTCTGTAAACTAGG 0 AACACACAGTGAGCATCGAGCTCTCA 0 - ILLUMINA NA 178 TRUE +KDR9 KDR9.chr4.55972964.55972964 KDR9.chr4.55972964.55972964_tile_1 Homo sapiens hg19 chr4 55972964 55972964 - TACCATGGTAGGCTGCGTTGGAAGTTA 0 GACAAACCCATACCCTTGTGAAGAATG 0 - ILLUMINA NA 172 TRUE +KDR10 KDR10.chr4.55979623.55979623 KDR10.chr4.55979623.55979623_tile_1 Homo sapiens hg19 chr4 55979623 55979623 - CTGGTGTCCCTGTTTTTAGCATTAAAT 0 ACCTAAAAACCCAGTCTGGGAGTGAG 0 - ILLUMINA NA 182 TRUE +KDR11 KDR11.chr4.55980348.55980348 KDR11.chr4.55980348.55980348_tile_1 Homo sapiens hg19 chr4 55980348 55980348 - TCTGTGCAAAGTTATAGGCTTATTTGC 0 AGAACTGAACTAAATGTGGGGATTGAC 0 - ILLUMINA NA 178 TRUE +FBXW7_1 FBXW7_1.chr4.153245446.153245446 FBXW7_1.chr4.153245446.153245446_tile_1 Homo sapiens hg19 chr4 153245446 153245446 - CAGTAATTGATAGGAAGAGTATCCATACT 0 AACAAGTGGAATGGAACTCAAAGACAA 0 - ILLUMINA NA 190 TRUE +FBXW7_2 FBXW7_2.chr4.153247288.153247366 FBXW7_2.chr4.153247288.153247366_tile_1 Homo sapiens hg19 chr4 153247288 153247366 - GTTTTGTTTTGTTTTTCTGTTTCTCCCT 0 TATGATGGCAGGAGGGTTGTTAGTGGAGCA 0 - ILLUMINA NA 171 TRUE +FBXW7_5 FBXW7_5.chr4.153249384.153249384 FBXW7_5.chr4.153249384.153249384_tile_1 Homo sapiens hg19 chr4 153249384 153249384 - CATACAGGTGGAGTATGGTCATCACAA 0 AAAAGGTAAGGGAAAATCTTGTCATGG 0 - ILLUMINA NA 184 TRUE +FBXW7_7 FBXW7_7.chr4.153250883.153250883 FBXW7_7.chr4.153250883.153250883_tile_1 Homo sapiens hg19 chr4 153250883 153250883 - CTGTTCCTGTTTATGCCTTCATTTTTC 0 AGTTAGTGGTTCTGATGACAACACTT 0 - ILLUMINA NA 180 TRUE +FBXW7_8 FBXW7_8.chr4.153258983.153258983 FBXW7_8.chr4.153258983.153258983_tile_1 Homo sapiens hg19 chr4 153258983 153258983 - CTGTAATTTGGGACATCTGTTAAAACAATA 0 GACTTCATTTCATTGCTCCCTAAAGAGG 0 - ILLUMINA NA 191 TRUE +APC1 APC1.chr5.112173917.112173917 APC1.chr5.112173917.112173917_tile_1 Homo sapiens hg19 chr5 112173917 112173917 - GCAGAGCTTCTTCTAAGTGCATTTCTC 0 TGAAGAAGTTCCTGGATTTTCTGTTGC 0 - ILLUMINA NA 186 TRUE +APC2 APC2.chr5.112174631.112174631 APC2.chr5.112174631.112174631_tile_1 Homo sapiens hg19 chr5 112174631 112174631 - AATTTGTTGGTCTCTCTTCTTCTTCAT 0 TTTGTTTCTGAACCATTGGCTCCCCGT 0 - ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_1 Homo sapiens hg19 chr5 112175162 112175958 + CTTGCAAAGTTTCTTCTATTAACCAAGA 0 TTCTGCTAATACCCTGCAAATAGCAGA 0 + ILLUMINA NA 176 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_2 Homo sapiens hg19 chr5 112175162 112175958 - TGCTGGATTTGGTTCTAGGGTGCT 0 CCTATTTCATCTTCAGCTGATGACAAA 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_3 Homo sapiens hg19 chr5 112175162 112175958 + GAAAAGATTGGAACTAGGTCAGCTGAAG 0 AGCGAAATCTCCCTCCAAAAGTGGT 0 + ILLUMINA NA 172 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_4 Homo sapiens hg19 chr5 112175162 112175958 - CTATCAAGTGAACTGACAGAAGTACATC 0 CCTGGCTGATTCTGAAGATAAACTAGAACC 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_5 Homo sapiens hg19 chr5 112175162 112175958 + CACCCAAAAGTCCACCTGAACACTAT 0 ATTATAAGCCCCAGTGATCTTCCAGAT 0 + ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_6 Homo sapiens hg19 chr5 112175162 112175958 - CTCTCTCTTTTCAGCAGTAGGTGCTT 0 CACTTACCATTCCACTGCATGGTTCA 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_7 Homo sapiens hg19 chr5 112175162 112175958 + CAAACCAAGCGAGAAGTACCTAAAAAT 0 AAAGTACTCCAGATGGATTTTCTTGTTC 0 + ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_8 Homo sapiens hg19 chr5 112175162 112175958 - CTCTGATTCTGTTTCATTCCCATTGTCATT 0 GTGGCAAAATGTAATAAAGTATCAGCATCT 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_9 Homo sapiens hg19 chr5 112175162 112175958 + ATTAAGAATAATGCCTCCAGTTCAGGA 0 AGAAGAATGTATTATTTCTGCCATGCC 0 + ILLUMINA NA 190 TRUE +CSF1R1_3 CSF1R1_3.chr5.149433644.149433646 CSF1R1_3.chr5.149433644.149433646_tile_1 Homo sapiens hg19 chr5 149433644 149433646 - TCCCACCCTCAGGACTATACCAATCT 0 AGTTCTGCTGAGGAGTTGACGACAGGG 0 - ILLUMINA NA 185 TRUE +CSF1R4 CSF1R4.chr5.149453044.149453044 CSF1R4.chr5.149453044.149453044_tile_1 Homo sapiens hg19 chr5 149453044 149453044 - TCTTGGGTGGTGGGGACTATGTACCT 0 AACTTGAGCTCTGAGCAGAACCTCATC 0 - ILLUMINA NA 175 TRUE +NPM1 NPM1.chr5.170837547.170837548 NPM1.chr5.170837547.170837548_tile_1 Homo sapiens hg19 chr5 170837547 170837548 - GGTAGGGAAAGTTCTCACTCTGCATTA 0 AAAAAGAAATGTGGTTAAGGAACCAC 0 - ILLUMINA NA 186 TRUE +EGFR1 EGFR1.chr7.55211080.55211080 EGFR1.chr7.55211080.55211080_tile_1 Homo sapiens hg19 chr7 55211080 55211080 - CATCGGAACTGCTGTCTGCATTTATGA 0 GATGATCTGCAGGTTTTCCAAAGGAAT 0 - ILLUMINA NA 188 TRUE +EGFR2 EGFR2.chr7.55221822.55221822 EGFR2.chr7.55221822.55221822_tile_1 Homo sapiens hg19 chr7 55221822 55221822 - AAGCAAGGCAAACACATCCACCCAAAG 0 AAAGCTGTATTTGCCCTCGGGGTTCA 0 - ILLUMINA NA 174 TRUE +EGFR3 EGFR3.chr7.55233043.55233043 EGFR3.chr7.55233043.55233043_tile_1 Homo sapiens hg19 chr7 55233043 55233043 - AACTTGGGAGACATTTTTGATCTCTGA 0 TGCCGGGCAGGTCTTGACGCAGT 0 - ILLUMINA NA 186 TRUE +EGFR4 EGFR4.chr7.55241677.55241708 EGFR4.chr7.55241677.55241708_tile_1 Homo sapiens hg19 chr7 55241677 55241708 - GGAAATATACAGCTTGCAAGGACTCTG 0 TCAAGATCCTCAAGAGAGCTTGGTTG 0 - ILLUMINA NA 180 TRUE +EGFR9 EGFR9.chr7.55242418.55242511 EGFR9.chr7.55242418.55242511_tile_1 Homo sapiens hg19 chr7 55242418 55242511 - ATGAGAAAAGGTGGGCCTGAGGTTCAG 0 CCTATGACAGAGAGAGAAGGAAGACGTT 0 - ILLUMINA NA 190 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_1 Homo sapiens hg19 chr7 55249005 55249131 - AGGTGAGGCAGATGCCCAGCAGGCGG 0 CGCATGAATGCGATCTTGAGTTTCAA 0 - ILLUMINA NA 175 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_2 Homo sapiens hg19 chr7 55249005 55249131 + CAGCGTGGACAACCCCCACGTGT 0 GTGTGTGCAGATCGCAAAGGTAATCA 0 + ILLUMINA NA 177 TRUE +EGFR54 EGFR54.chr7.55259514.55259524 EGFR54.chr7.55259514.55259524_tile_1 Homo sapiens hg19 chr7 55259514 55259524 - CCTCCCCTGCATGTGTTAAACAATACA 0 CCAAAATCTGTGATCTTGACATGCTGC 0 - ILLUMINA NA 178 TRUE +MET1 MET1.chr7.116339642.116339642 MET1.chr7.116339642.116339642_tile_1 Homo sapiens hg19 chr7 116339642 116339642 - CCTTCTCACTGATATCGAATGCAATGG 0 CTTCTATCTGTGGGGAGAATATGCAGT 0 - ILLUMINA NA 180 TRUE +MET2 MET2.chr7.116340262.116340262 MET2.chr7.116340262.116340262_tile_1 Homo sapiens hg19 chr7 116340262 116340262 - GCCCTGGATATTCTTTTTGAGACTGAT 0 GAAGAAGTCGTTGACATATTTGATAGG 0 - ILLUMINA NA 188 TRUE +MET3 MET3.chr7.116411990.116411990 MET3.chr7.116411990.116411990_tile_1 Homo sapiens hg19 chr7 116411990 116411990 - TGCAAAACCAAAAATAAACAACAATGTC 0 TTACACTTCGGGCACTTACAAGCCTA 0 - ILLUMINA NA 171 TRUE +MET4 MET4.chr7.116417463.116417464 MET4.chr7.116417463.116417464_tile_1 Homo sapiens hg19 chr7 116417463 116417464 - CACAAGGGGAAAGTGTAAATCAACGTTT 0 CACAACCAAAATGCCCTGTGCAAAAGA 0 - ILLUMINA NA 191 TRUE +MET6 MET6.chr7.116423413.116423474 MET6.chr7.116423413.116423474_tile_1 Homo sapiens hg19 chr7 116423413 116423474 - GAGGAGAAACTCAGAGATAACCAATAC 0 TGTCTCTGGCAAGACCAAAATCAGCA 0 - ILLUMINA NA 172 TRUE +SMO1 SMO1.chr7.128845101.128845101 SMO1.chr7.128845101.128845101_tile_1 Homo sapiens hg19 chr7 128845101 128845101 - TGACCAGGGTGAAGAGCGTGCAGAG 0 AAGGGCACTTCGCACTGGCCTGAA 0 - ILLUMINA NA 186 TRUE +SMO2 SMO2.chr7.128846040.128846040 SMO2.chr7.128846040.128846040_tile_1 Homo sapiens hg19 chr7 128846040 128846040 - ATTGCCACAGTGAGGACAAAGGGGAGT 0 GTACACGATGACAAAGATGATGACGCA 0 - ILLUMINA NA 186 TRUE +SMO3 SMO3.chr7.128846374.128846374 SMO3.chr7.128846374.128846374_tile_1 Homo sapiens hg19 chr7 128846374 128846374 - TAGCTGGGGTTTCAGCATGGGGGCAGC 0 AAGCCCGCACGGTATCGGTAGTTCT 0 - ILLUMINA NA 190 TRUE +SMO4 SMO4.chr7.128850341.128850341 SMO4.chr7.128850341.128850341_tile_1 Homo sapiens hg19 chr7 128850341 128850341 - AACCACTGACCAAGGCTGTGCTAGAGG 0 TCATGGCGATGCCAGTTCCAAACA 0 - ILLUMINA NA 190 TRUE +SMO5 SMO5.chr7.128851593.128851593 SMO5.chr7.128851593.128851593_tile_1 Homo sapiens hg19 chr7 128851593 128851593 - TTCAGATCCTCTGGGGCCTTTCCTTC 0 AGAAATATCCTGGGGCAGTATGGCTCC 0 - ILLUMINA NA 173 TRUE +BRAF1 BRAF1.chr7.140453121.140453193 BRAF1.chr7.140453121.140453193_tile_1 Homo sapiens hg19 chr7 140453121 140453193 - ACCTAAACTCTTCATAATGCTTGCTCT 0 GGTCCCATCAGTTTGAACAGTTGTCT 0 - ILLUMINA NA 176 TRUE +BRAF28 BRAF28.chr7.140481397.140481478 BRAF28.chr7.140481397.140481478_tile_1 Homo sapiens hg19 chr7 140481397 140481478 - GGTTTTCTTTTTCTGTTTGGCTTGACT 0 CTACAAGGGAAAGTGGCATGGTAAGTA 0 - ILLUMINA NA 178 TRUE +FGFR1_1 FGFR1_1.chr8.38282209.38282209 FGFR1_1.chr8.38282209.38282209_tile_1 Homo sapiens hg19 chr8 38282209 38282209 - TTTTGAGAGGCTTGGGCTCAGCAGAA 0 TCACCGGCCCATCCTGCAAGCAGGG 0 - ILLUMINA NA 179 TRUE +FGFR1_2 FGFR1_2.chr8.38285938.38285938 FGFR1_2.chr8.38285938.38285938_tile_1 Homo sapiens hg19 chr8 38285938 38285938 - AAGAGATCATCACTAAGGGAGCAGTGG 0 GGATGATGATGATGATGATGACTCCTC 0 - ILLUMINA NA 184 TRUE +JAK2_1 JAK2_1.chr9.5073769.5073770 JAK2_1.chr9.5073769.5073770_tile_1 Homo sapiens hg19 chr9 5073769 5073770 - TTCAGTTTCAAAAATACTTAACTCCTGTT 0 CTCCATAATTTAAAACCAAATGCTTGTG 0 - ILLUMINA NA 188 TRUE +CDKN2A1 CDKN2A1.chr9.21971153.21971187 CDKN2A1.chr9.21971153.21971187_tile_1 Homo sapiens hg19 chr9 21971153 21971187 - TTGTGTGGGGGTCTGCTTGGCGGTGA 0 AACTGCGCCGACCCCGCCACTCTCA 0 - ILLUMINA NA 187 TRUE +ABL1_1 ABL1_1.chr9.133738330.133738364 ABL1_1.chr9.133738330.133738364_tile_1 Homo sapiens hg19 chr9 133738330 133738364 - ATGCATCGCCTAATGCCAGCAGACGC 0 TGATGTCCGTGCGTTCCATCTCCCAC 0 - ILLUMINA NA 191 TRUE +ABL1_9 ABL1_9.chr9.133747520.133747520 ABL1_9.chr9.133747520.133747520_tile_1 Homo sapiens hg19 chr9 133747520 133747520 - AGCGCCTGTGTCACCCTGGGGGT 0 AAAACGAAGGTGAAATTATTTCAGGAA 0 - ILLUMINA NA 190 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_1 Homo sapiens hg19 chr9 133748283 133748414 + AGAATCCTTCAGAAGGCTTTTTCTTTAGAC 0 AACCTCCTGGACTACCTGAGGGAGT 0 + ILLUMINA NA 172 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_2 Homo sapiens hg19 chr9 133748283 133748414 - TCCATGGCGCAGGCTGCCTGGCC 0 CCGTAGGTCATGAACTCAGTGATGA 0 - ILLUMINA NA 182 TRUE +ABL1_16 ABL1_16.chr9.133750356.133750356 ABL1_16.chr9.133750356.133750356_tile_1 Homo sapiens hg19 chr9 133750356 133750356 - GGGAAGAGCAAGAAAGAGGCAGAAAAA 0 TGTGTAGGTGTCCCCTGTCATCAA 0 - ILLUMINA NA 190 TRUE +NOTCH1_1 NOTCH1_1.chr9.139397768.139397768 NOTCH1_1.chr9.139397768.139397768_tile_1 Homo sapiens hg19 chr9 139397768 139397768 - AGACCTGGCTTCCCACCACCCCAGGCT 0 AGATTGACAACCGGCAGTGTGTGCAG 0 - ILLUMINA NA 190 TRUE +NOTCH1_2 NOTCH1_2.chr9.139399344.139399422 NOTCH1_2.chr9.139399344.139399422_tile_1 Homo sapiens hg19 chr9 139399344 139399422 - AGTGCGAGTGGGACGGGCTGGACTGT 0 ACACCAACGTGGTCTTCAAGCGTGAC 0 - ILLUMINA NA 171 TRUE +RET1 RET1.chr10.43609078.43609104 RET1.chr10.43609078.43609104_tile_1 Homo sapiens hg19 chr10 43609078 43609104 - ACTCGCCTCCCAGCAATTTCCTCCC 0 TTGCAGGTGCCATAGCCAGCTTTAAT 0 - ILLUMINA NA 180 TRUE +RET2_9 RET2_9.chr10.43609940.43609950 RET2_9.chr10.43609940.43609950_tile_1 Homo sapiens hg19 chr10 43609940 43609950 + AAGCCTCACACCACCCCCACCCACAGAT 0 CCCATCTCCTCAGCTGAGATGACCTT 0 + ILLUMINA NA 175 TRUE +RET10 RET10.chr10.43613840.43613840 RET10.chr10.43613840.43613840_tile_1 Homo sapiens hg19 chr10 43613840 43613840 - AGAACAGGGCTGTATGGAGCCCCCAGC 0 GGGAGGCGTTCTCTGAAATGCAG 0 - ILLUMINA NA 190 TRUE +RET11_12 RET11_12.chr10.43615567.43615569 RET11_12.chr10.43615567.43615569_tile_1 Homo sapiens hg19 chr10 43615567 43615569 - ATGGTGCACCTGGGATCCCTGGGAG 0 ATGTTTCTGGCTGCCAAGTCCCGATGAA 0 - ILLUMINA NA 172 TRUE +RET13 RET13.chr10.43617416.43617416 RET13.chr10.43617416.43617416_tile_1 Homo sapiens hg19 chr10 43617416 43617416 - AATTCCCTGGCCAAGCTGCACAGACGG 0 CCATTTAACTGGAATCCGACCCTAAAG 0 - ILLUMINA NA 178 TRUE +PTEN1 PTEN1.chr10.89624242.89624244 PTEN1.chr10.89624242.89624244_tile_1 Homo sapiens hg19 chr10 89624242 89624244 - TACGGACATTTTCGCATCCGTCTACTC 0 ATGATGGCTGTCATGTCTGGGAGCCTG 0 - ILLUMINA NA 176 TRUE +PTEN3 PTEN3.chr10.89685307.89685307 PTEN3.chr10.89685307.89685307_tile_1 Homo sapiens hg19 chr10 89685307 89685307 - TGGACTTCTTGACTTAATCGGTTTAGG 0 CTTGTAATGGTTTTTATGCTTTGAATCCA 0 - ILLUMINA NA 186 TRUE +PTEN4 PTEN4.chr10.89711893.89711900 PTEN4.chr10.89711893.89711900_tile_1 Homo sapiens hg19 chr10 89711893 89711900 - GGATGAGAATTTCAAGCACTTACTGCA 0 TGGGAATAGTTACTCCCTGGTGGACA 0 - ILLUMINA NA 176 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_1 Homo sapiens hg19 chr10 89717615 89717772 - GGGTCCTGAATTGGAGGAATATATCTTCAC 0 ACACGAAATATGGATTCTGTATCTGC 0 - ILLUMINA NA 181 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_2 Homo sapiens hg19 chr10 89717615 89717772 + CAGTTTGTGGTCTGCCAGCTAAA 0 AAAGGTTTGTACTTTACTTTCATTGGGAG 0 + ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_1 Homo sapiens hg19 chr10 89720716 89720852 - AATTTGGAGAAAAGTATCGGTTGGCTT 0 AGGTTTCCTCTGGTCCTGGTATGAA 0 - ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_2 Homo sapiens hg19 chr10 89720716 89720852 + AAAATGATCTTGACAAAGCAAATAAAGAC 0 CTTGCTTGACAAGTTTTTAACTTATGTATT 0 + ILLUMINA NA 179 TRUE +FGFR2_1 FGFR2_1.chr10.123258034.123258034 FGFR2_1.chr10.123258034.123258034_tile_1 Homo sapiens hg19 chr10 123258034 123258034 - CTAACAGTAGCTGCCCATGAGTTAGAG 0 TTCTTGGAGCCTGCACACAGGATGGTG 0 - ILLUMINA NA 180 TRUE +FGFR2_2 FGFR2_2.chr10.123274774.123274803 FGFR2_2.chr10.123274774.123274803_tile_1 Homo sapiens hg19 chr10 123274774 123274803 - GCCTTTTGGTTCCTTTGGTTGTGCTAT 0 CATAGGGGTCTTCTTAATCGCCTGTAT 0 - ILLUMINA NA 186 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_1 Homo sapiens hg19 chr10 123279503 123279677 - CACGTGGAAAAGAACGGCAGTAAATAC 0 GGAGTTGAGAGAGGATGATTCTCTTTT 0 - ILLUMINA NA 172 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_2 Homo sapiens hg19 chr10 123279503 123279677 + TTTAGATTCAGAAAGTCCTCACCTTGAG 0 CTCCTCCGACCACTGTGGAGGCATTT 0 + ILLUMINA NA 171 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_3 Homo sapiens hg19 chr10 123279503 123279677 - ACTGACAGCCCTCTGGACAACACAGCT 0 CGTAGAGTTTGTCTGCAAGGTTTACAG 0 - ILLUMINA NA 184 TRUE +HRAS1 HRAS1.chr11.533873.533875 HRAS1.chr11.533873.533875_tile_1 Homo sapiens hg19 chr11 533873 533875 - TACCAGGGAGAGGCTGGCTGTGTGAAC 0 AGTACAGCGCCATGCGGGACCAGTAC 0 - ILLUMINA NA 180 TRUE +HRAS6 HRAS6.chr11.534285.534289 HRAS6.chr11.534285.534289_tile_1 Homo sapiens hg19 chr11 534285 534289 - CTGCCCTGTGGGGCCTGGGGCTGG 0 AAGAGTGCGCTGACCATCCAGCTGATC 0 - ILLUMINA NA 185 TRUE +ATM1 ATM1.chr11.108117847.108117848 ATM1.chr11.108117847.108117848_tile_1 Homo sapiens hg19 chr11 108117847 108117848 - GAAAGGAATAGTTGCATGTACAGAGTC 0 GATATCTGCCATCAATTCAATCAAATTTT 0 - ILLUMINA NA 174 TRUE +ATM2 ATM2.chr11.108119823.108119823 ATM2.chr11.108119823.108119823_tile_1 Homo sapiens hg19 chr11 108119823 108119823 - TTGCTAGTAATAGGTTTGGGGGTAGAC 0 GATCAAAATCATTCTGTGACTTCTGAA 0 - ILLUMINA NA 172 TRUE +ATM3 ATM3.chr11.108123551.108123551 ATM3.chr11.108123551.108123551_tile_1 Homo sapiens hg19 chr11 108123551 108123551 - AAGCTATAGCTTAAAATGATAAAGAGCAT 0 ACAAAGAAAAACAAAAAGCTTCACTTAGA 0 - ILLUMINA NA 172 TRUE +ATM4 ATM4.chr11.108137973.108138003 ATM4.chr11.108137973.108138003_tile_1 Homo sapiens hg19 chr11 108137973 108138003 - ACTGCCAAATCAATATAAAGAAGTAAAAGA 0 GATTTCCATTAGTATCATCTTCCATTGAT 0 - ILLUMINA NA 189 TRUE +ATM6 ATM6.chr11.108155132.108155132 ATM6.chr11.108155132.108155132_tile_1 Homo sapiens hg19 chr11 108155132 108155132 - TCGAATAAATAGCCTTAAAACTTAAAGGTT 0 ATCCCACTGTCTCTGGTACCCTCATAG 0 - ILLUMINA NA 179 TRUE +ATM7 ATM7.chr11.108170476.108170479 ATM7.chr11.108170476.108170479_tile_1 Homo sapiens hg19 chr11 108170476 108170479 - ACTCACCAATCTTCTACCAGTGTGTTA 0 ACTTCTCCCAAGCAGCTTCCAACAGCC 0 - ILLUMINA NA 178 TRUE +ATM9 ATM9.chr11.108172421.108172421 ATM9.chr11.108172421.108172421_tile_1 Homo sapiens hg19 chr11 108172421 108172421 - ACAGAACTGTTTTAGATATGCTGGGTA 0 AATGTTTTTCAAACAGGTAACAGCTGC 0 - ILLUMINA NA 182 TRUE +ATM10 ATM10.chr11.108173640.108173640 ATM10.chr11.108173640.108173640_tile_1 Homo sapiens hg19 chr11 108173640 108173640 - CAGGTCATAAACAAGGAATTATATCAGACT 0 ATATCATCCAGGCCTTCAAAAGGG 0 - ILLUMINA NA 191 TRUE +ATM11 ATM11.chr11.108180945.108180945 ATM11.chr11.108180945.108180945_tile_1 Homo sapiens hg19 chr11 108180945 108180945 - CCCTTATTGAGACAATGCCAACATTAA 0 CTAGATAATTTAAATCCAGCCAGAAAGC 0 - ILLUMINA NA 188 TRUE +ATM12 ATM12.chr11.108200958.108200961 ATM12.chr11.108200958.108200961_tile_1 Homo sapiens hg19 chr11 108200958 108200961 - CAAAGTCGGAATACCCACATATCATGT 0 CCTTTACTGTGTATCTTGCATAGAATAAT 0 - ILLUMINA NA 172 TRUE +ATM14 ATM14.chr11.108204681.108204681 ATM14.chr11.108204681.108204681_tile_1 Homo sapiens hg19 chr11 108204681 108204681 - TAGGTTGAAACATATGAAATTTGCCAA 0 GGGACAACAACATCTTCTAAATTCTTAAG 0 - ILLUMINA NA 174 TRUE +ATM15 ATM15.chr11.108205769.108205769 ATM15.chr11.108205769.108205769_tile_1 Homo sapiens hg19 chr11 108205769 108205769 - GACAAAATCCCAAATAAAGCAGAAAGAA 0 CCTGCTAAGCGAAATTCTGCTTTAAATG 0 - ILLUMINA NA 191 TRUE +ATM16 ATM16.chr11.108206594.108206594 ATM16.chr11.108206594.108206594_tile_1 Homo sapiens hg19 chr11 108206594 108206594 - CACCCAACCAAATGGCATCTTTTATAT 0 TTGTCTCAGGTCATCACGGCCCTTCAG 0 - ILLUMINA NA 186 TRUE +ATM17 ATM17.chr11.108218089.108218089 ATM17.chr11.108218089.108218089_tile_1 Homo sapiens hg19 chr11 108218089 108218089 - CTAGGACAACTGTTTATGCTGAAAACA 0 TCTATATGTACAAGTTCTGCTGACTGC 0 - ILLUMINA NA 188 TRUE +ATM18 ATM18.chr11.108225590.108225590 ATM18.chr11.108225590.108225590_tile_1 Homo sapiens hg19 chr11 108225590 108225590 - GCTAAGTGCACAATCTCCTCCTTTCT 0 AACAGAGTTTCCTGAGAGTTTCTCATC 0 - ILLUMINA NA 191 TRUE +ATM19 ATM19.chr11.108236086.108236203 ATM19.chr11.108236086.108236203_tile_1 Homo sapiens hg19 chr11 108236086 108236203 - TGAAGATCACACCCAAGCTTTCCATC 0 TCAGCTACTTTGTTGAAACTCTGGTCA 0 - ILLUMINA NA 185 TRUE +KRAS1 KRAS1.chr12.25378562.25378562 KRAS1.chr12.25378562.25378562_tile_1 Homo sapiens hg19 chr12 25378562 25378562 - TCTTTCCCAGAGAACAAATTAAAAGAGT 0 AGACAAGACAGGTAAGTAACACTGAAA 0 - ILLUMINA NA 187 TRUE +KRAS2 KRAS2.chr12.25380275.25380283 KRAS2.chr12.25380275.25380283_tile_1 Homo sapiens hg19 chr12 25380275 25380283 - TTGTTGTTGAGTTGTATATAACACCTTTT 0 AGTACAGTGCAATGAGGGACCAGTAC 0 - ILLUMINA NA 184 TRUE +KRAS7 KRAS7.chr12.25398255.25398285 KRAS7.chr12.25398255.25398285_tile_1 Homo sapiens hg19 chr12 25398255 25398285 - GGTACTGGTGGAGTATTTGATAGTGTAT 0 GCTAATTCAGAATCATTTTGTGGACGAAT 0 - ILLUMINA NA 191 TRUE +PTPN11_1 PTPN11_1.chr12.112888163.112888211 PTPN11_1.chr12.112888163.112888211_tile_1 Homo sapiens hg19 chr12 112888163 112888211 - TACTGACCTTTCAGAGGTAGGATCTGC 0 GTGTTCTGAATCTTGATGTGGGTGAC 0 - ILLUMINA NA 190 TRUE +PTPN11_10 PTPN11_10.chr12.112926884.112926888 PTPN11_10.chr12.112926884.112926888_tile_1 Homo sapiens hg19 chr12 112926884 112926888 - CAAGAGGCCTAGCAAGAGAATGAGAAT 0 TCTGAGACCGCACCATCTGGATGGTT 0 - ILLUMINA NA 178 TRUE +HNF1A_1 HNF1A_1.chr12.121431413.121431414 HNF1A_1.chr12.121431413.121431414_tile_1 Homo sapiens hg19 chr12 121431413 121431414 - TTGCCGCAGCCCAGACCAAACCAGCA 0 TTGAAACGGTTCCTCCGCCCCTTCTT 0 - ILLUMINA NA 175 TRUE +HNF1A_3 HNF1A_3.chr12.121432070.121432070 HNF1A_3.chr12.121432070.121432070_tile_1 Homo sapiens hg19 chr12 121432070 121432070 - ACATACCACTTACCGTGGACCTTACT 0 CGGTTGGCAAACCAGTTGTAGACA 0 - ILLUMINA NA 181 TRUE +FLT3_1 FLT3_1.chr13.28592620.28592653 FLT3_1.chr13.28592620.28592653_tile_1 Homo sapiens hg19 chr13 28592620 28592653 - CACATCACAGTAAATAACACTCTGGTG 0 TTGTCAGGGGCAATGTGAGGCTGCTATT 0 - ILLUMINA NA 178 TRUE +FLT3_13 FLT3_13.chr13.28602329.28602329 FLT3_13.chr13.28602329.28602329_tile_1 Homo sapiens hg19 chr13 28602329 28602329 - ACTTGAGTTTTACATTTTTAATGCTCCT 0 TGTCAGGTAACCCACTTCCACGAAAA 0 - ILLUMINA NA 171 TRUE +FLT3_14 FLT3_14.chr13.28608244.28608341 FLT3_14.chr13.28608244.28608341_tile_1 Homo sapiens hg19 chr13 28608244 28608341 - CTATCTGCAGAACTGCCTATTCCTAAC 0 TTCCAAGAGAAAATTTAGAGTTTGGTAAG 0 - ILLUMINA NA 190 TRUE +FLT3_22 FLT3_22.chr13.28610138.28610138 FLT3_22.chr13.28610138.28610138_tile_1 Homo sapiens hg19 chr13 28610138 28610138 + CCAGGTCCAAGATGGTAATGGGTAT 0 ATACCAATACTTTGTGAAGCCAAGGTGG 0 + ILLUMINA NA 171 TRUE +RB1_1 RB1_1.chr13.48919244.48919244 RB1_1.chr13.48919244.48919244_tile_1 Homo sapiens hg19 chr13 48919244 48919244 - CCTTTCCAATTTGCTGAAGAGTGCAAA 0 CAGTAACCTTAAAAATTTGTGTTATTTCGT 0 - ILLUMINA NA 182 TRUE +RB1_2 RB1_2.chr13.48923148.48923148 RB1_2.chr13.48923148.48923148_tile_1 Homo sapiens hg19 chr13 48923148 48923148 - GCTAACAGTTAATAAGCCAAGCAGAGA 0 AAATGTGATCCAAGAAACTTTTAGCAC 0 - ILLUMINA NA 178 TRUE +RB1_3 RB1_3.chr13.48942685.48942685 RB1_3.chr13.48942685.48942685_tile_1 Homo sapiens hg19 chr13 48942685 48942685 - ACATAAAGAAACGTGAACAAATCTGAAA 0 GGTGTTCTCTGTGTTTCAAAACTAAATAA 0 - ILLUMINA NA 173 TRUE +RB1_4 RB1_4.chr13.48955538.48955550 RB1_4.chr13.48955538.48955550_tile_1 Homo sapiens hg19 chr13 48955538 48955550 - TTCCCTATATGTTCTTGAGGTAGATGT 0 AATGTTTTATCATTTCTCTTGTCAAGTTG 0 - ILLUMINA NA 182 TRUE +RB1_6 RB1_6.chr13.49027168.49027168 RB1_6.chr13.49027168.49027168_tile_1 Homo sapiens hg19 chr13 49027168 49027168 - TTTGCAGTTTGAATGGTCAACATAACA 0 TAAAGGTGAATCCTATATGAAACATGATG 0 - ILLUMINA NA 178 TRUE +RB1_7 RB1_7.chr13.49033843.49033846 RB1_7.chr13.49033843.49033846_tile_1 Homo sapiens hg19 chr13 49033843 49033846 - GAAGTGCTTGATTTTCTTACTTGGTCC 0 TAGGCTAGCCGATACACTGTGGGAATA 0 - ILLUMINA NA 178 TRUE +RB1_8 RB1_8.chr13.49037877.49037877 RB1_8.chr13.49037877.49037877_tile_1 Homo sapiens hg19 chr13 49037877 49037877 - GGAAAATTACCTACCTCCTGAACAGCA 0 AGTAGTCAGAATTTTATTACATGGTTTTGT 0 - ILLUMINA NA 172 TRUE +RB1_9 RB1_9.chr13.49039164.49039164 RB1_9.chr13.49039164.49039164_tile_1 Homo sapiens hg19 chr13 49039164 49039164 - TGTTTTGGTGGACCCATTACATTAGAT 0 CTTTGATCAAAACACGTTTGAATGTCT 0 - ILLUMINA NA 174 TRUE +AKT1 AKT1.chr14.105246455.105246455 AKT1.chr14.105246455.105246455_tile_1 Homo sapiens hg19 chr14 105246455 105246455 - TCTGACGGGTAGAGTGTGCGTGGCTC 0 GCTCCCCTCAACAACTTCTCTGTG 0 - ILLUMINA NA 173 TRUE +CDH1_1 CDH1_1.chr16.68835649.68835650 CDH1_1.chr16.68835649.68835650_tile_1 Homo sapiens hg19 chr16 68835649 68835650 - GGCGGTGGTGGTGCCCCACTGT 0 CTTTGAATCGGGTGTCGAGGGAAAAA 0 - ILLUMINA NA 171 TRUE +CDH1_2 CDH1_2.chr16.68846137.68846137 CDH1_2.chr16.68846137.68846137_tile_1 Homo sapiens hg19 chr16 68846137 68846137 - ACATTCTCTAGTCTGGAGAGAGTTTTC 0 TTGGTGTCAGTGACTGTGATCACAGCT 0 - ILLUMINA NA 176 TRUE +CDH1_3 CDH1_3.chr16.68847274.68847277 CDH1_3.chr16.68847274.68847277_tile_1 Homo sapiens hg19 chr16 68847274 68847277 - CATCTTGCCAGGTACCATACAAACCTT 0 CACTTTCAGTGTGGTGATTACGACGTT 0 - ILLUMINA NA 178 TRUE +TP53_1 TP53_1.chr17.7574003.7574021 TP53_1.chr17.7574003.7574021_tile_1 Homo sapiens hg19 chr17 7574003 7574021 - ACTAAATGCATGTTGCTTTTGTACCGT 0 AGAGCTGAATGAGGCCTTGGAACTC 0 - ILLUMINA NA 172 TRUE +TP53_3 TP53_3.chr17.7577022.7577129 TP53_3.chr17.7577022.7577129_tile_1 Homo sapiens hg19 chr17 7577022 7577129 - ATCCTGAGTAGTGGTAATCTACTGGGA 0 AGGTAAGCAAGCAGGACAAGAAGCG 0 - ILLUMINA NA 172 TRUE +TP53_17 TP53_17.chr17.7577523.7577574 TP53_17.chr17.7577523.7577574_tile_1 Homo sapiens hg19 chr17 7577523 7577574 - AAAAAGGCCTCCCCTGCTTGCCACAGG 0 ATCATCACACTGGAAGACTCCAGGTCA 0 - ILLUMINA NA 190 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_1 Homo sapiens hg19 chr17 7578190 7578536 - TTTGGATGACAGAAACACTTTTCGACA 0 CCTGCTGCTTATTTGACCTCCCTATAAC 0 - ILLUMINA NA 172 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_2 Homo sapiens hg19 chr17 7578190 7578536 + GACCCCAGTTGCAAACCAGACCTCA 0 TGAGGAATCAGAGGCCTGGGGA 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_3 Homo sapiens hg19 chr17 7578190 7578536 - TTGTGAGGCGCTGCCCCCACCATGAG 0 GCATCTTATCCGAGTGGAAGGAAATTTG 0 - ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_4 Homo sapiens hg19 chr17 7578190 7578536 + CGTCTCTCCAGCCCCAGCTGCTCACCAT 0 CCACAGCTGCACAGGGCAGGTCTT 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_5 Homo sapiens hg19 chr17 7578190 7578536 - GCATGTTTGTTTCTTTGCTGCCGTCT 0 TTGATTCCACACCCCCGCCCGGC 0 - ILLUMINA NA 179 TRUE +TP53_60 TP53_60.chr17.7579358.7579403 TP53_60.chr17.7579358.7579403_tile_1 Homo sapiens hg19 chr17 7579358 7579403 - AGATGAAGCTCCCAGAATGCCAGAGG 0 TTCTTGCATTCTGGGACAGCCAAGTCT 0 - ILLUMINA NA 185 TRUE +TP53_64 TP53_64.chr17.7579882.7579882 TP53_64.chr17.7579882.7579882_tile_1 Homo sapiens hg19 chr17 7579882 7579882 - ATGGTGTTGGGGGAGGGGGTTCCTTCT 0 CCCCTCTGAGTCAGGAAACATTTTCAG 0 - ILLUMINA NA 182 TRUE +ERBB2_1 ERBB2_1.chr17.37880219.37880261 ERBB2_1.chr17.37880219.37880261_tile_1 Homo sapiens hg19 chr17 37880219 37880261 - CATATCTCCCCAAACCCCAATGAAGAG 0 CTTTGATGGCCACTGGAATTTTCACA 0 - ILLUMINA NA 172 TRUE +ERBB2_4 ERBB2_4.chr17.37880993.37881012 ERBB2_4.chr17.37880993.37881012_tile_1 Homo sapiens hg19 chr17 37880993 37881012 - ATACACCAGTTCAGCAGGTCCTGGGAG 0 TATGCTTCCTGGGGACAAGGGTAC 0 - ILLUMINA NA 190 TRUE +ERBB2_13 ERBB2_13.chr17.37881332.37881440 ERBB2_13.chr17.37881332.37881440_tile_1 Homo sapiens hg19 chr17 37881332 37881440 - TCTGCTCCTTGGTCCTTCACCTAACCT 0 ACATCCTCCAGGTAGCTCATCCCCTGG 0 - ILLUMINA NA 186 TRUE +SMAD4_1 SMAD4_1.chr18.48575169.48575170 SMAD4_1.chr18.48575169.48575170_tile_1 Homo sapiens hg19 chr18 48575169 48575170 - TACAAAAATTGAAACACTATTGAGATCCT 0 CGCATACTGACAATATTTAACATGTTTTAG 0 - ILLUMINA NA 172 TRUE +SMAD4_2 SMAD4_2.chr18.48581198.48581198 SMAD4_2.chr18.48581198.48581198_tile_1 Homo sapiens hg19 chr18 48581198 48581198 - ATGTTGGGAAAGTTGGCAGTGCTGGTA 0 CAAAGTCATGCACATATTCATCCTTCAC 0 - ILLUMINA NA 180 TRUE +SMAD4_3 SMAD4_3.chr18.48584560.48584560 SMAD4_3.chr18.48584560.48584560_tile_1 Homo sapiens hg19 chr18 48584560 48584560 - GCTGTCTAAAAATTAAGGCCCACATGG 0 TGATGCTATCTGCAACAGTCCTTCAC 0 - ILLUMINA NA 188 TRUE +SMAD4_4 SMAD4_4.chr18.48586262.48586262 SMAD4_4.chr18.48586262.48586262_tile_1 Homo sapiens hg19 chr18 48586262 48586262 - ACTCATGTCATGATGAGTATTGTACTC 0 AATGCAAGCTCATTGTGAACAGGCCCT 0 - ILLUMINA NA 184 TRUE +SMAD4_5 SMAD4_5.chr18.48591826.48591919 SMAD4_5.chr18.48591826.48591919_tile_1 Homo sapiens hg19 chr18 48591826 48591919 - CAATACCTTGCTCTCTCAATGGCTTCT 0 AGTAAGCAATGGAACACCAATACTCAG 0 - ILLUMINA NA 188 TRUE +SMAD4_11 SMAD4_11.chr18.48593405.48593405 SMAD4_11.chr18.48593405.48593405_tile_1 Homo sapiens hg19 chr18 48593405 48593405 - GCACTTGGGTAGATCTTATGAACAGCA 0 TGCCTATGTGCAACCTTAGGAAGAAA 0 - ILLUMINA NA 172 TRUE +SMAD4_12 SMAD4_12.chr18.48603032.48603094 SMAD4_12.chr18.48603032.48603094_tile_1 Homo sapiens hg19 chr18 48603032 48603094 - AAAGAATGAAAAGCATACTTACTGATAGC 0 CTGACGCAAATCAAAGACCTTTTAAGAA 0 - ILLUMINA NA 172 TRUE +SMAD4_15 SMAD4_15.chr18.48604668.48604754 SMAD4_15.chr18.48604668.48604754_tile_1 Homo sapiens hg19 chr18 48604668 48604754 - GCATGGTATGAAGTACTTCGTCTAGGA 0 AAGGTCATCAACACCAATTCCAGCAG 0 - ILLUMINA NA 172 TRUE +STK11_1 STK11_1.chr19.1207021.1207092 STK11_1.chr19.1207021.1207092_tile_1 Homo sapiens hg19 chr19 1207021 1207092 - CGCAACTTCTTCTTCTTGAGGATCTTG 0 TAGATGACCTCGGTGGAGTCGATGCGG 0 - ILLUMINA NA 178 TRUE +STK11_4 STK11_4.chr19.1220487.1220502 STK11_4.chr19.1220487.1220502_tile_1 Homo sapiens hg19 chr19 1220487 1220502 - AAAGCCGGGGAGCCCTGGCTGGTC 0 AGATTTTGAGGGTGCCACCGGTGGTG 0 - ILLUMINA NA 181 TRUE +STK11_8 STK11_8.chr19.1221264.1221319 STK11_8.chr19.1221264.1221319_tile_1 Homo sapiens hg19 chr19 1221264 1221319 + TGTACCCCTTCGAAGGGGACAACATCTA 0 GCTTTTGTGCAGAAATGTAGGGTTGG 0 + ILLUMINA NA 177 TRUE +STK11_12 STK11_12.chr19.1223059.1223125 STK11_12.chr19.1223059.1223125_tile_1 Homo sapiens hg19 chr19 1223059 1223125 - ACATCCTGGCCGAGTCAGCAGAGCC 0 ACCGGTCCTTGGTGTCTGGGCTC 0 - ILLUMINA NA 188 TRUE +JAK3_1 JAK3_1.chr19.17945696.17945696 JAK3_1.chr19.17945696.17945696_tile_1 Homo sapiens hg19 chr19 17945696 17945696 - ATCCCTGATCCCACTTTCATTCCCTCA 0 ATGCCCATCAGTGCCCTGGATCCTG 0 - ILLUMINA NA 176 TRUE +JAK3_2 JAK3_2.chr19.17948009.17948009 JAK3_2.chr19.17948009.17948009_tile_1 Homo sapiens hg19 chr19 17948009 17948009 - TAGTGCTGTGTGCACTAATGGCAGACT 0 AGCTTGATGAGCCAAGTGTCGTAC 0 - ILLUMINA NA 190 TRUE +SRC SRC.chr20.36031762.36031762 SRC.chr20.36031762.36031762_tile_1 Homo sapiens hg19 chr20 36031762 36031762 - AAAGAGGAAGGGCCTCGCCCCTGGCAAT 0 TACTGGGGCTCGGTGGACGTGAAGTAG 0 - ILLUMINA NA 191 TRUE +GNAS1 GNAS1.chr20.57484420.57484421 GNAS1.chr20.57484420.57484421_tile_1 Homo sapiens hg19 chr20 57484420 57484421 - ACAGCTGGTTATTCCAGAGGGACTGGG 0 GCGAAGCAGGTCCTGAAACAAAATTGA 0 - ILLUMINA NA 172 TRUE +SMARCB1_1 SMARCB1_1.chr22.24133967.24133990 SMARCB1_1.chr22.24133967.24133990_tile_1 Homo sapiens hg19 chr22 24133967 24133990 - GCGAGTGGTTTTGAAACAGGTTTACA 0 ACATACGGAGGTAGTTTCCCACCTAT 0 - ILLUMINA NA 189 TRUE +SMARCB1_3 SMARCB1_3.chr22.24143240.24143240 SMARCB1_3.chr22.24143240.24143240_tile_1 Homo sapiens hg19 chr22 24143240 24143240 - TTGTGGGGAGCACAAGGTCAAAGCAG 0 ATGCGGTTCCTGTTGATGGTTGTGGA 0 - ILLUMINA NA 175 TRUE +SMARCB1_4 SMARCB1_4.chr22.24145582.24145582 SMARCB1_4.chr22.24145582.24145582_tile_1 Homo sapiens hg19 chr22 24145582 24145582 - ATGTCCTGCGTGTCAGGTCCAGAATCT 0 TTCTGCCCATCGATCTCCATGTCCAG 0 - ILLUMINA NA 176 TRUE +SMARCB1_5_6 SMARCB1_5_6.chr22.24176352.24176357 SMARCB1_5_6.chr22.24176352.24176357_tile_1 Homo sapiens hg19 chr22 24176352 24176357 - ACTCCACCCCCACCCGATCCTCAGGA 0 TGTTGGCAAGACGCCTCATCCGCCTGG 0 - ILLUMINA NA 173 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_1 Homo sapiens hg19 chr19 3114942 3115070 + AGTGCGCGGTCCACCCCCTCCT 0 CTGCCCACCCAGCAGGACGTGCT 0 + ILLUMINA NA 182 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_2 Homo sapiens hg19 chr19 3114942 3115070 - CGGCACACCGGGCAAATGAGCC 0 TAGCCCAAGGTGGCGATGCGGTC 0 - ILLUMINA NA 177 TRUE +GNA11_5 GNA11_5.chr19.3118922.3119051 GNA11_5.chr19.3118922.3119051_tile_1 Homo sapiens hg19 chr19 3118922 3119051 + TCCTGCTCCAGCCGATGTCAGTCT 0 GATCCACTGCTTTGAGAACGTGACAT 0 + ILLUMINA NA 189 TRUE +GNA11_6 GNA11_6.chr19.3119204.3119357 GNA11_6.chr19.3119204.3119357_tile_2 Homo sapiens hg19 chr19 3119204 3119357 + GGATGGAGGAGAGCAAAGCCCTGTT 0 CATGGGGAGGGGCTCGCGGGCA 0 + ILLUMINA NA 189 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_1 Homo sapiens hg19 chr19 3120987 3121177 - AACATCTTCAGGATGAACTCCCGCGCC 0 ACGGCCCACCCAGCTCGACCCCC 0 - ILLUMINA NA 172 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_2 Homo sapiens hg19 chr19 3120987 3121177 + AGGTCCCCAGCGGGACGCCCAG 0 CAGCTCAACCTCAAGGAGTACAACCT 0 + ILLUMINA NA 187 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_3 Homo sapiens hg19 chr19 3120987 3121177 - AAAAATCTCCTCCCGCGGGCAGAG 0 AGGATGGTGTCCTTCACGGCCGC 0 - ILLUMINA NA 185 TRUE +GNAQ_4 GNAQ_4.chr9.80412436.80412564 GNAQ_4.chr9.80412436.80412564_tile_1 Homo sapiens hg19 chr9 80412436 80412564 - CATTCTCATTGTGTCTTCCCTCCTCTA 0 GTAACTGAGTCCATGAAACCTATTTCC 0 - ILLUMINA NA 188 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_1 Homo sapiens hg19 chr9 80409379 80409508 - GCTTAGTGAATATGATCAAGTTCTCGTGG 0 GCTTTCTTGAAATTTGATTTTAGGACTTTT 0 - ILLUMINA NA 174 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_2 Homo sapiens hg19 chr9 80409379 80409508 + AGATAATAAAATGATAATCCATTGCCTGTC 0 TTGGCCCCCTACATCGACCATTCT 0 + ILLUMINA NA 177 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_3 Homo sapiens hg19 chr9 80409379 80409508 - ATTGAATTGACTTGGATGATCATCGTC 0 GGTCAGAGAGAAGAAAATGGATACACT 0 - ILLUMINA NA 182 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_1 Homo sapiens hg19 chr9 80343430 80343583 - GAAAATCATGTATTCCCATCTAGTCGACT 0 TTGCCCTGTGCAGCCTGCGTGTTGA 0 - ILLUMINA NA 172 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_2 Homo sapiens hg19 chr9 80343430 80343583 + TTCACAGCTACTGAGCTGTGGTATGA 0 AGGGGTATGTGATAATTGTTCTAAAGAGAG 0 + ILLUMINA NA 171 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_3 Homo sapiens hg19 chr9 80343430 80343583 - GGTCGTATACAAAAGATGGGTTGGACTTAT 0 GTTCCAGAACTCCTCGGTTATTCTGTT 0 - ILLUMINA NA 187 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_1 Homo sapiens hg19 chr9 80336240 80336429 - ACCATCCTCCAGTTGAACCTGAAGG 0 TTTATTGCCGTCCTGGACTCTGTGTGAGCG 0 - ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_2 Homo sapiens hg19 chr9 80336240 80336429 + CAGGGAAGGGCAGGGCGGGTGTCTA 0 ATAATTTTGTCACTGTCTGGGTTCAGG 0 + ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_3 Homo sapiens hg19 chr9 80336240 80336429 - CCAATGATGATTGAATACATTAGCAGAT 0 TACTCCCACTTCACGTGCGCCACAGAC 0 - ILLUMINA NA 177 TRUE +[Targets] +TargetA TargetB Target Number Chromosome Start Position End Position Probe Strand Sequence Species Build ID +MPL1_2.chr1.43815008.43815009_tile_1 MPL1_2.chr1.43815008.43815009_tile_1 1 chr1 43814982 43815163 + GGTGGCAGTTTCCTGCACACTACAGGTACCGCCCCCGCCAGGCAGGAGACTGGCGGTGGACCAGGTGGAGCCGAAGGCCTGTAAACAGGCATTCTTGGTTCGCTCTGTGACCCCAGATCTCCGTCCACCGCC Homo sapiens hg19 +NRAS1_7.chr1.115256528.115256531_tile_1 NRAS1_7.chr1.115256528.115256531_tile_1 1 chr1 115256500 115256680 + TCTTGTCCAGCTGTATCCAGTATGTCCAACAAACAGGTTTCACCATCTATAACCACTTGTTTTCTGTAAGAATCCTGGGGGTGTGGAGGGTAAGGGGGCAGGGAGGGAGGGAAGTTCAATTTTTATTA Homo sapiens hg19 +NRAS8_13.chr1.115258730.115258748_tile_1 NRAS8_13.chr1.115258730.115258748_tile_1 1 chr1 115258702 115258884 + TGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACACCAGCAAGAACCTGTTGGAAACCAGTAATCAGGGTTAATTGGCGAGCCACATCTACAGTACTTTAAAG Homo sapiens hg19 +ALK1.chr2.29432664.29432664_tile_1 ALK1.chr2.29432664.29432664_tile_1 1 chr2 29432636 29432822 + TCGGGCCATCCCGAAGTCTCCAATCTTGGCCACTCTTCCAGGGCCTGGACAGGTCAAGAGGCAGTTTCTGGCAGCAATGTCTCTGGGAAGAAAGGAAATGCATTTCCTAATTTTATCCCTAGGAAGATGAGTG Homo sapiens hg19 +ALK2.chr2.29443695.29443695_tile_1 ALK2.chr2.29443695.29443695_tile_1 1 chr2 29443667 29443836 + GTTGAATTTGCTGCAGAGCAGAGAGGGATGTAACCAAAATTAACTGAGCTGAGTCTGGGCAAATCTTAAACTGGGAGGAACAGGATACAAAGTTACATTTTCAGCAGCTACAATGTATA Homo sapiens hg19 +IDH1_1_2.chr2.209113112.209113113_tile_1 IDH1_1_2.chr2.209113112.209113113_tile_1 1 chr2 209113084 209113264 + ACGACCTATGATGATAGGTTTTACCCATCCACTCACAAGCCGGGGGATATTTTTGCAGATAATGGCTTCTCTGAAGACCGTGCCACCCAGAATATTTCGTATGGTGCCATTTGGTGATTTCCACATT Homo sapiens hg19 +ERBB4_1_2.chr2.212288942.212288955_tile_1 ERBB4_1_2.chr2.212288942.212288955_tile_1 1 chr2 212288912 212289100 + CCTTTCTCTAATAAATCAGGGATTTCTCGCGTTGGAATTCCATCATAGGGTTTTCCTCCAAAGGTCATCAGTTCCCATATAGTAACTCCTATATTGGAGAAAAAATTCTTACTTAAGCATATTAACAACATATGT Homo sapiens hg19 +ERBB4_3_4.chr2.212530066.212530135_tile_1 ERBB4_3_4.chr2.212530066.212530135_tile_1 1 chr2 212530036 212530210 + TGGATGGCATGGGTGGCACTCCCGATCTGGATCAGCATACTTGAAAATGAAACTGTTTGCCCCCTGTAAGCCATCTGGACATTTTTCCACACAGTTTGGGCCATCTTTAAAATGAGAGCACT Homo sapiens hg19 +ERBB4_5.chr2.212576857.212576857_tile_1 ERBB4_5.chr2.212576857.212576857_tile_1 1 chr2 212576821 212576990 + AATCCACAGTCTGAGCTGACATCAATGATCCTGTGCCAATGCCATCACAAGCTGTAGAAACAAGACTCAGAGTTAGGGGATTGAGAAACTTATTTTTGGCCAATAAATCA Homo sapiens hg19 +ERBB4_6_7.chr2.212578341.212578349_tile_1 ERBB4_6_7.chr2.212578341.212578349_tile_1 1 chr2 212578315 212578499 + CGCACACAAGAACTGGAATCTACCACAAAGTTATCTGATTAAAAAAAAAAAAAAGGTAAAATAAGCATTAATGTTAACATTCAGCAAACAAGCTCAAAACAAGATATTTTAGGGTTTAAAAATGATTAGCA Homo sapiens hg19 +ERBB4_8.chr2.212587147.212587147_tile_1 ERBB4_8.chr2.212587147.212587147_tile_1 1 chr2 212587115 212587285 + CTCCATATGTGTACTTTGCATTGAAATTGTGCTCCAGTTGAAAGGTGGTTGGATTGTAGACAAAGGTTTGGGGACACTGAGTAACACATGCTCCACTGTCATTGAAATTCATGCAGG Homo sapiens hg19 +ERBB4_9.chr2.212589811.212589811_tile_1 ERBB4_9.chr2.212589811.212589811_tile_1 1 chr2 212589783 212589957 + TGTGTCCTTAGGTCCTGAGCAGCCTCCAGCACATTCTCGATGGCAGCAGTCACTGACGTAAGGTCCGTAGCATCTGCCGTCACATTGTTCTGCACACACCGTCCTTGTCACTGCAGAAGAC Homo sapiens hg19 +ERBB4_10.chr2.212652764.212652764_tile_1 ERBB4_10.chr2.212652764.212652764_tile_1 1 chr2 212652706 212652876 + ATAATTCTACTTACATCCTGAACTACCATTTGTTGACACAAGAGTCAAGTTGGAAGGCCATGGGTTCCGAACAATATCTTGCCAATGAATGGTGTCTGCATAACAAAGGAATTT Homo sapiens hg19 +ERBB4_11.chr2.212812157.212812157_tile_1 ERBB4_11.chr2.212812157.212812157_tile_1 1 chr2 212812127 212812311 + TGTCAAGTTCTTTAATCCAAGTTCTTGAAGTCCAAAGTTTCCATCTTTTCTGTAGTTTAAAAATATTGCCAAGGCATATCGATCCTCATAAAGTTTTGTCCCACGAATAATGCGTAAATTCTCCAGAGG Homo sapiens hg19 +VHL1_2.chr3.10183797.10183817_tile_1 VHL1_2.chr3.10183797.10183817_tile_1 1 chr3 10183769 10183952 + GGCTCAACTTCGACGGCGAGCCGCAGCCCTACCCAACGCTGCCGCCTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAGGCCCGACCCAGCAGGGACGATAGCACGGTCTGAAGC Homo sapiens hg19 +VHL3_5.chr3.10188245.10188301_tile_1 VHL3_5.chr3.10188245.10188301_tile_1 1 chr3 10188217 10188401 + GGTTAACCAAACTGAATTATTTGTGCCATCTCTCAATGTTGACGGACAGCCTATTTTTGCCAATATCACACTGCCAGGTACTGACGTTTTACTTTTTAAAAAGATAAGGTTGTTGTGGTAAGTACAGGATA Homo sapiens hg19 +VHL6_8.chr3.10191480.10191506_tile_1 VHL6_8.chr3.10191480.10191506_tile_1 1 chr3 10191450 10191634 + TCTGAAAGAGCGATGCCTCCAGGTTGTCCGGAGCCTAGTCAAGCCTGAGAATTACAGGAGACTGGACATCGTCAGGTCGCTCTACGAAGATCTGGAAGACCACCCAAATGTGCAGAAAGACCTGGAGCGG Homo sapiens hg19 +MLH1.chr3.37067240.37067240_tile_1 MLH1.chr3.37067240.37067240_tile_1 1 chr3 37067212 37067394 + GGTTCGTACAGATTCCCGGGAACAGAAGCTTGATGCATTTCTGCAGCCTCTGAGCAAACCCCTGTCCAGTCAGCCCCAGGCCATTGTCACAGAGGATAAGACAGATATTTCTAGTGGCAGGGCTAGGCAG Homo sapiens hg19 +CTNNB1_1_16.chr3.41266040.41266137_tile_1 CTNNB1_1_16.chr3.41266040.41266137_tile_1 1 chr3 41266010 41266180 + ATGGCCATGGAACCAGACAGAAAAGCGGCTGTTAGTCACTGGCAGCAACAGTCTTACCTGGACTCTGGAATCCATTCTGGTGCCACTACCACAGCTCCTTCTCTGAGTGGTAAAGGC Homo sapiens hg19 +PIK3CA1.chr3.178916876.178916876_tile_1 PIK3CA1.chr3.178916876.178916876_tile_1 1 chr3 178916836 178917024 + TGATGAAACAAGACGACTTTGTGACCTTCGGCTTTTTCAACCCTTTTTAAAAGTAATTGAACCAGTAGGCAACCGTGAAGAAAAGATCCTCAATCGAGAAATTGGTATGATACAATATCCTATTCTAAAATGCAAA Homo sapiens hg19 +PIK3CA2.chr3.178921553.178921553_tile_1 PIK3CA2.chr3.178921553.178921553_tile_1 1 chr3 178921525 178921709 + ATGTAAATATTCGAGACATTGATAAGGTAAAGTCAAATGCTGATGCTTATTATTTTATAGAAATTATTTTAGATAACCTTTTTCTTGCACTATACAGTAATCTGTTGACCTGTAGTATGTTTTCAGATGGT Homo sapiens hg19 +PIK3CA3.chr3.178927980.178927980_tile_1 PIK3CA3.chr3.178927980.178927980_tile_1 1 chr3 178927906 178928082 + TTATAATTTAGACTAGTGAATATTTTTCTTTGTTTTTTAAGGAACACTGTCCATTGGCATGGGGAAATATAAACTTGTTTGATTACACAGACACTCTAGTATCTGGAAAAATGGCTTTGAATC Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 1 chr3 178936044 178936214 + ATCCTCTCTCTGAAATCACTGAGCAGGAGAAAGATTTTCTATGGAGTCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGAATTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 1 chr3 178938832 178939004 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTCTCAAACAGGAGAAGAAGGATGAAACACAAAAGGTGTGTGACTCTAGTTTGTGTTTGAGACTCTT Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_1 PIK3CA13_20.chr3.178952007.178952150_tile_1 1 chr3 178951881 178952054 + TATCTAGCTATTCGACAGCATGCCAATCTCTTCATAAATCTTTTCTCAATGATGCTTGGCTCTGGAATGCCAGAACTACAATCTTTTGATGACATTGCATACATTCGAAAGACCCTAGCC Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_2 PIK3CA13_20.chr3.178952007.178952150_tile_2 1 chr3 178951999 178952184 - TTTCAGTTCAATGCATGCTGTTTAATTGTGTGGAAGATCCAATCCATTTTTGTTGTCCAGCCACCATGATGTGCATCATTCATTTGTTTCATGAAATACTCCAAAGCCTCTTGCTCAGTTTTATCTAAG Homo sapiens hg19 +FGFR3_1_2.chr4.1803564.1803568_tile_1 FGFR3_1_2.chr4.1803564.1803568_tile_1 1 chr4 1803538 1803712 + GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTGCCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTGGAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCCACATCCAGTGGCT Homo sapiens hg19 +FGFR3_3_4.chr4.1806119.1806153_tile_1 FGFR3_3_4.chr4.1806119.1806153_tile_1 1 chr4 1806091 1806277 + CGGGGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTGTGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGGCCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCCCGCTCAAGCGACAGGTA Homo sapiens hg19 +FGFR3_5_7.chr4.1807862.1807890_tile_1 FGFR3_5_7.chr4.1807862.1807890_tile_1 1 chr4 1807836 1808025 + CCGGGACGTGCACAACCTCGACTACTACAAGAAGACGACCAACGTGAGCCCGGCCCTGGGGTGCGGGGGTGGGGGTCATGCCAGTAGGACGCCTGGCGCCAACACCGCCTTCCCACACCCTCCCAGGGCCGGCTGCCCGTGA Homo sapiens hg19 +FGFR3_8.chr4.1808331.1808331_tile_1 FGFR3_8.chr4.1808331.1808331_tile_1 1 chr4 1808295 1808464 + GCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCTTCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCCCGCCAACTGCACACACGACCTGTGAGTGGCATCCCTGGCCCTCCACTGGGTCC Homo sapiens hg19 +FGFR3_9.chr4.1808949.1808949_tile_1 FGFR3_9.chr4.1808949.1808949_tile_1 1 chr4 1808921 1809105 + CCTGCTGCCCCCGGCCCCACCCAGCAGTGGGGGCTCGCGGACGTGAAGGGCCACTGGTCCCCAACAATGTGAGGGGTCCCTAGCAGCCCACCCTGCTGCTGGTGCACAGCCACTCCCCGGCATGAGACTCAGTGC Homo sapiens hg19 +PDGFRA1_4.chr4.55141013.55141049_tile_1 PDGFRA1_4.chr4.55141013.55141049_tile_1 1 chr4 55140981 55141157 + AAACCGAGGTATGAAATTCGCTGGAGGGTCATTGAATCAATCAGCCCAGATGGACATGAATATATTTATGTGGACCCGATGCAGCTGCCTTATGACTCAAGATGGGAGTTTCCAAGAGATGGA Homo sapiens hg19 +PDGFRA5.chr4.55144146.55144146_tile_1 PDGFRA5.chr4.55144146.55144146_tile_1 1 chr4 55144120 55144306 + AACTTGCTGGGAGCCTGCACCAAGTCAGGTGGGCTCACTGACCTGGAGTGAGGATTTTCACTGGACACATGTGGTTGTGAAAACTGTTCAATCAGGCTTAAATCCTCCACTCTCCATCCCCACACATGGCAGGG Homo sapiens hg19 +PDGFRA6.chr4.55144547.55144547_tile_1 PDGFRA6.chr4.55144547.55144547_tile_1 1 chr4 55144519 55144703 + CACAGAGTATTGCTTCTATGGAGATTTGGTCAACTATTTGCATAAGAATAGGGATAGCTTCCTGAGCCACCACCCAGAGAAGCCAAAGAAAGAGCTGGATATCTTTGGATTGAACCCTGCTGATGAAAGCAC Homo sapiens hg19 +PDGFRA7_23.chr4.55152040.55152109_tile_1 PDGFRA7_23.chr4.55152040.55152109_tile_1 1 chr4 55152012 55152184 + CGTCCTCCTGGCACAAGGAAAAATTGTGAAGATCTGTGACTTTGGCCTGGCCAGAGACATCATGCATGATTCGAACTATGTGTCGAAAGGCAGTGTACGTCCTCACTTCCCTCACTGGTCA Homo sapiens hg19 +KIT1.chr4.55561764.55561764_tile_1 KIT1.chr4.55561764.55561764_tile_1 1 chr4 55561736 55561913 + CGACGAGATTAGGCTGTTATGCACTGATCCGGGCTTTGTCAAATGGACTTTTGAGATCCTGGATGAAACGAATGAGAATAAGCAGAATGAATGGATCACGGAAAAGGCAGAAGCCACCAACACCG Homo sapiens hg19 +KIT2.chr4.55592185.55592186_tile_1 KIT2.chr4.55592185.55592186_tile_1 1 chr4 55592155 55592341 + CCTATTTTAACTTTGCATTTAAAGGTAACAACAAAGGTATATTTCTTTTTAATCCAATTTAAGGGGATGTTTAGGCTCTGTCTACCATATCAGTCATGATTTTAAGTTCATTCCAACATTGACCATGTCATTTC Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_1 KIT3_19.chr4.55593464.55593689_tile_1 1 chr4 55593342 55593512 + ATTTCTCTTCCATTGTAGAGCAAATCCATCCCCACACCCTGTTCACTCCTTTGCTGATTGGTTTCGTAATCGTAGCTGGCATGATGTGCATTATTGTGATGATTCTGACCTACAAATA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_2 KIT3_19.chr4.55593464.55593689_tile_2 1 chr4 55593436 55593609 - TTCTGTGGGGAGAAAGGGAAAAATAGATCACCTTTTAATAATTATTGTCTCAGTCATTAGAGCACTCTGGAGAGAGAACAAATAAATGGTTACCTGTAAATATTTGTAGGTCAGAATCATCA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_3 KIT3_19.chr4.55593464.55593689_tile_3 1 chr4 55593556 55593739 + AACCCATGTATGAAGTACAGTGGAAGGTTGTTGAGGAGATAAATGGAAACAATTATGTTTACATAGACCCAACACAACTTCCTTATGATCACAAATGGGAGTTTCCCAGAAACAGGCTGAGTTTTGGTCAG Homo sapiens hg19 +KIT20_21.chr4.55594221.55594258_tile_1 KIT20_21.chr4.55594221.55594258_tile_1 1 chr4 55594193 55594380 + CAAAGTCCTGAGTTACCTTGGTAATCACATGAATATTGTGAATCTACTTGGAGCCTGCACCATTGGAGGTAAAGCCGTGTCCAAGCTGCCTTTTATTGTCTGTCAGGTTATCAAAACATGACATTTTAATATG Homo sapiens hg19 +KIT22.chr4.55595519.55595519_tile_1 KIT22.chr4.55595519.55595519_tile_1 1 chr4 55595493 55595675 + CAGAATATTGTTGCTATGGTGATCTTTTGAATTTTTTGAGAAGAAAACGTGATTCATTTATTTGTTCAAAGCAGGAAGATCATGCAGAAGCTGCACTTTATAAGAATCTTCTGCATTCAAAGGAGTCT Homo sapiens hg19 +KIT23.chr4.55597495.55597497_tile_1 KIT23.chr4.55597495.55597497_tile_1 1 chr4 55597467 55597652 + CAGCGATAGTACTAATGAGTACATGGACATGAAACCTGGAGTTTCTTATGTTGTCCCAACCAAGGCCGACAAAAGGAGATCTGTGAGAATAGGTGAGTACCTACCTATCAAGCAACCAAGAGTAACTTTAC Homo sapiens hg19 +KIT24_28.chr4.55599320.55599348_tile_1 KIT24_28.chr4.55599320.55599348_tile_1 1 chr4 55599290 55599472 + AGAGACATCAAGAATGATTCTAATTATGTGGTTAAAGGAAACGTGAGTACCCATTCTCTGCTTGACAGTCCTGCAAAGGATTTTTAGTTTCAACTTTCGATAAAAATTGTTTCCTGTGATTTTCATAAT Homo sapiens hg19 +KIT29.chr4.55602694.55602694_tile_1 KIT29.chr4.55602694.55602694_tile_1 1 chr4 55602666 55602850 + CCTGAAAGCATTTTCAACTGTGTATACACGTTTGAAAGTGACGTCTGGTCCTATGGGATTTTTCTTTGGGAGCTGTTCTCTTTAGGTAAAATGATCCTTGCCAAAGACAACTTCATTAGACTCAGAGCATCTT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_1 KDR1.chr4.55946114.55946257_tile_1 1 chr4 55945984 55946155 + CGGCTACTTCCTGCTGGTGGAAAGAACAACACTTGAAAATCTGAGCAGCACCTCTCATGTGATGTCCAGGAGTTGGGGGTGTGGATGCTTCCTTTTAAACAGGAGGAGAGCT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_2 KDR1.chr4.55946114.55946257_tile_2 1 chr4 55946098 55946284 - GGATATCACTCCGATGACACAGACACCACCGTGTACTCCAGTGAGGAAGCAGAACTTTTAAAGCTGATAGAGATTGGAGTGCAAACCGGTAGCACAGCCCAGATTCTCCAGCCTGACTCGGGGACCACACTGA Homo sapiens hg19 +KDR3.chr4.55953807.55953807_tile_1 KDR3.chr4.55953807.55953807_tile_1 1 chr4 55953777 55953965 + TTGGGGTCACATACTTCCTCCTCCTCCATACAGGAAACAGGTGAGGTAGGCAGAGAGAGTCCAGAATCCTCTTCCATGCTCAAAGTCTCTGATATCGGAAGAACAATGTAGTCTTTGCCATCCTGAAACAATAAA Homo sapiens hg19 +KDR4.chr4.55955111.55955127_tile_1 KDR4.chr4.55955111.55955127_tile_1 1 chr4 55955085 55955257 + CCCCGTGCCAGCAGTCCAGCATGGTCTGGTACCTAGAGAAGCAAAACACTGATTTCATTAAATGCCTCTTTCTTCCTGAATGCTGAAAATAAGCACTTAAATGAGTACACATTTGTAAAGAG Homo sapiens hg19 +KDR6.chr4.55960989.55961023_tile_1 KDR6.chr4.55960989.55961023_tile_1 1 chr4 55960959 55961129 + TCACTGAGGGACTTCTCCTCCACAAATCCAGAGCTGGCTGAGCTCTGGCTACTGGTGATGCTGTCCAAGCGCCGTTTCAGATCCACAGGGATTGCTCCAACGTAGTCTTTCCCTTGA Homo sapiens hg19 +KDR8.chr4.55962507.55962507_tile_1 KDR8.chr4.55962507.55962507_tile_1 1 chr4 55962477 55962653 + GCTCCTTCTACAAATACAGTACAAAGAGGGAAATCATAGGTATGGACATTTCCTTCAATAATTGGGGTCCCTCCCTCCCTGCATGCCACTATACAACTTACCCTCCGGGGTAACACAGCTGTGA Homo sapiens hg19 +KDR9.chr4.55972964.55972964_tile_1 KDR9.chr4.55972964.55972964_tile_1 1 chr4 55972936 55973106 + ACTGAGACAGCTTGGCTATAAGAAAGAGATAACAGCGCATATTATGATTTAATTTTTCTTTAATTAGAGTCAAGAGTAAGGAAAAGATTCAGACTTTGGTTATTCTGTTCTTAGAAA Homo sapiens hg19 +KDR10.chr4.55979623.55979623_tile_1 KDR10.chr4.55979623.55979623_tile_1 1 chr4 55979595 55979775 + CTCGGTTTACAAGTTTCTTATGCTGATGCTGAAAAAAAGAGTTGACTGAACTTCCAAAGCACAGCATATAACATTACCCAATAACTTCTAGTAACACACAGAATTAAATCTGGGCTTTGGTAAACATT Homo sapiens hg19 +KDR11.chr4.55980348.55980348_tile_1 KDR11.chr4.55980348.55980348_tile_1 1 chr4 55980320 55980496 + TGCTGTACAATTTAAGACAAGCTTTTCTCCAACAGATAGTTCAATTCCATGAGACGGACTCAGAACCACATCATAAATCCTATACCCTAGAGCAAGTAAATTGAAAAAACAGAACATGAGAGA Homo sapiens hg19 +FBXW7_1.chr4.153245446.153245446_tile_1 FBXW7_1.chr4.153245446.153245446_tile_1 1 chr4 153245416 153245604 + AACGACTGGTGCCCTGTTAACGTGTGAATGCAATTCCCTGTCTCCACATCCCAAACACGGATTGATGTATCAAGAGATCCACTCACCACATGGATACCATCAAACTACAAAAGACACAGTTTATTAGAATAGA Homo sapiens hg19 +FBXW7_2.chr4.153247288.153247366_tile_1 FBXW7_2.chr4.153247288.153247366_tile_1 1 chr4 153247248 153247417 + TTGAACACAGCGGACTGCTGCAACATGACCCATCAAAACATGTAAACACTGGCCTGTCTCAATATCCCAAACCCTAAGAGTGGCATCTCGAGAACCGCTAACAACTCTGCAG Homo sapiens hg19 +FBXW7_5.chr4.153249384.153249384_tile_1 FBXW7_5.chr4.153249384.153249384_tile_1 1 chr4 153249338 153249520 + TTCATGAAGATGCATACAACGCACAGTGGAAGTATGCCCATATAAGGTGTGTATACATTCTCCAGTCTCTGCATTCCACACTTTGAGTGTCCGATCTGTAGATCCACTAATGATGATGTTGTCTCTCAT Homo sapiens hg19 +FBXW7_7.chr4.153250883.153250883_tile_1 FBXW7_7.chr4.153250883.153250883_tile_1 1 chr4 153250853 153251031 + ATTCGGTTACCACAAAACTGTAAGCATGTGATCACATGATCATCATGTCCTTTCAGCACCTATAAGAAAGATGTGCAGATTAGAAATATGTTAATTAAATTATGTTCTTTAAAATACTGGTGAAGA Homo sapiens hg19 +FBXW7_8.chr4.153258983.153258983_tile_1 FBXW7_8.chr4.153258983.153258983_tile_1 1 chr4 153258953 153259142 + TCGTTGAAACTGGGGTTCTATCACTTGCATCATATGTTTTACTTGTGTTGGTTCACAACTATCAATGAGTTCATCTAAAGCAAGCAATTTCTCTGGTCCACTCCAGCTCTATCAAAGAGAATTAGAAATTTT Homo sapiens hg19 +APC1.chr5.112173917.112173917_tile_1 APC1.chr5.112173917.112173917_tile_1 1 chr5 112173887 112174071 + AAGCGAGGTTTGCAGATCTCCACCACTGCAGCCCAGATTGCCAAAGTCATGGAAGAAGTGTCAGCCATTCATACCTCTCAGGAAGACAGAAGTTCTGGGTCTACCACTGAATTACATTGTGTGACAGATGA Homo sapiens hg19 +APC2.chr5.112174631.112174631_tile_1 APC2.chr5.112174631.112174631_tile_1 1 chr5 112174603 112174775 + TCGAGTGGGTTCTAATCATGGAATTAATCAAAATGTAAGCCAGTCTTTGTGTCAAGAAGATGACTATGAAGATGATAAGCCTACCAATTATAGTGAACGTTACTCTGAAGAAGAACAGC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_1 APC3_42.chr5.112175162.112175958_tile_1 1 chr5 112175034 112175208 - TCTGCTTCCTGTGTCGTCTGATTACATCCTATTTCATCTTCAGCTGATGACAAAGATGATAATGAACTACATCTTGAAAAACATATTGGAGTATCTTCTACACAATAAGTCTGTATTGTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_2 APC3_42.chr5.112175162.112175958_tile_2 1 chr5 112175128 112175297 + ATGTAATCAGACGACACAGGAAGCAGATTCTGCTAATACCCTGCAAATAGCAGAAATAAAAGAAAAGATTGGAACTAGGTCAGCTGAAGATCCTGTGAGCGAAGTTCCAGCAGTGTCAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_3 APC3_42.chr5.112175162.112175958_tile_3 1 chr5 112175216 112175386 - CCTGAAGAAAATTCAACAGCTTTGTGCCTGGCTGATTCTGAAGATAAACTAGAACCCTGCAGTCTGCTGGATTTGGTTCTAGGGTGCTGTGACACTGCTGGAACTTCGCTCACAGGAT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_4 APC3_42.chr5.112175162.112175958_tile_4 1 chr5 112175306 112175475 + CACAAAGCTGTTGAATTTTCTTCAGGAGCGAAATCTCCCTCCAAAAGTGGTGCTCAGACACCCAAAAGTCCACCTGAACACTATGTTCAGGAGACCCCACTCATGTTTAGCA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_5 APC3_42.chr5.112175162.112175958_tile_5 1 chr5 112175394 112175566 - GCCACTTACCATTCCACTGCATGGTTCACTCTGAACGGAGCTGGCAATCGAACGACTCTCAAAACTATCAAGTGAACTGACAGAAGTACATCTGCTAAACATGAGTGGGGTCTCCTGAAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_6 APC3_42.chr5.112175162.112175958_tile_6 1 chr5 112175512 112175683 + GCATTATAAGCCCCAGTGATCTTCCAGATAGCCCTGGACAAACCATGCCACCAAGCAGAAGTAAAACACCTCCACCACCTCCTCAAACAGCTCAAACCAAGCGAGAAGTACCTAAAAATA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_7 APC3_42.chr5.112175162.112175958_tile_7 1 chr5 112175630 112175799 - CCGTGGCAAAATGTAATAAAGTATCAGCATCTGGAAGAACCTGGACCCTCTGAACTGCAGCATTTACTGCAGCTTGCTTAGGTCCACTCTCTCTCTTTTCAGCAGTAGGTGCTTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_8 APC3_42.chr5.112175162.112175958_tile_8 1 chr5 112175740 112175911 + GGAAAGTACTCCAGATGGATTTTCTTGTTCATCCAGCCTGAGTGCTCTGAGCCTCGATGAGCCATTTATACAGAAAGATGTGGAATTAAGAATAATGCCTCCAGTTCAGGAA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_9 APC3_42.chr5.112175162.112175958_tile_9 1 chr5 112175854 112176042 - AGTATTTCAATATCATCATCATCTGAATCATCTAATAGGTCCTTTTCAGAATCAATAGTTTTTTCTGCCTCTTTCTCTTGGTTTTCATTTGATTCTTTAGGCTGCTCTGATTCTGTTTCATTCCCATTGTCATTT Homo sapiens hg19 +CSF1R1_3.chr5.149433644.149433646_tile_1 CSF1R1_3.chr5.149433644.149433646_tile_1 1 chr5 149433616 149433799 + GATAGTTGTTGGGCTGCAGCAAGGGCTGGGCGATATCCCCTTGCTCGCAGCAGGTCAGGTGCTCACTAGAGCTCTCCTCCTCCAGCTCACTGCTGCTGCTGCCGCTGCCACCGCTTCTGCTGCTGCTCGGC Homo sapiens hg19 +CSF1R4.chr5.149453044.149453044_tile_1 CSF1R4.chr5.149453044.149453044_tile_1 1 chr5 149453016 149453189 + CAAGTAGGCACTCTCTGGAAAGCAGAACACACAAGCATCTGGCATTAGTGGGAAGATGTCCTTGTTTATTTGTCCATTTTGTCATCCACCCATTGATCCAGTCCCTGAGCAGCTATGTCAC Homo sapiens hg19 +NPM1.chr5.170837547.170837548_tile_1 NPM1.chr5.170837547.170837548_tile_1 1 chr5 170837493 170837677 + TTTTTTTTCCAGGCTATTCAAGATCTCTGGCAGTGGAGGAAGTCTCTTTAAGAAAATAGTTTAAACAATTTGTTAAAAAATTTTCCGTCTTATTTCATTTCTGTAACAGTTGATATCTGGCTGTCCTTTTTA Homo sapiens hg19 +EGFR1.chr7.55211080.55211080_tile_1 EGFR1.chr7.55211080.55211080_tile_1 1 chr7 55211052 55211238 + AGAGGAAATATGTACTACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATGATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAGAAATTTACAGGGTGAGAGGCTGGGATGCCAAGGCTGGGGGT Homo sapiens hg19 +EGFR2.chr7.55221822.55221822_tile_1 EGFR2.chr7.55221822.55221822_tile_1 1 chr7 55221792 55221964 + GGTGCCACCTGCGTGAAGAAGTGTCCCCGTGAGTCCTCCTCTGTGGGCCCTCTAACTGGTCAGGCATCCTTGTCCCGCTCTGTCTCCTGCTGAGCCCTGGAGTATCCCATCTTGGAGAGT Homo sapiens hg19 +EGFR3.chr7.55233043.55233043_tile_1 EGFR3.chr7.55233043.55233043_tile_1 1 chr7 55233019 55233203 + GGAGTCATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCAGACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTGCACCTACGGGTGAGTGGAAAGTGAAGGAGAACAGAACATTTCCTCTCTTGCAAAT Homo sapiens hg19 +EGFR4.chr7.55241677.55241708_tile_1 EGFR4.chr7.55241677.55241708_tile_1 1 chr7 55241649 55241827 + AGGAAACTGAATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTTCGGCACGGTGTATAAGGTAAGGTCCCTGGCACAGGCCTCTGGGCTGGGCCGCAGGGCCTCTCATGGTCTGGTGGGGAGCC Homo sapiens hg19 +EGFR9.chr7.55242418.55242511_tile_1 EGFR9.chr7.55242418.55242511_tile_1 1 chr7 55242388 55242576 + GACTCTGGATCCCAGAAGGTGAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCTCGATGTGAGTTTCTGCTTTGCTGTGTGGGGGTCCATGGCT Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_1 EGFR44.chr7.55249005.55249131_tile_1 1 chr7 55248879 55249052 + TCTTCACCTGGAAGGGGTCCATGTGCCCCTCCTTCTGGCCACCATGCGAAGCCACACTGACGTGCCTCTCCCTCCCTCCAGGAAGCCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTG Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_2 EGFR44.chr7.55249005.55249131_tile_2 1 chr7 55249003 55249178 - CAGTTGAGCAGGTACTGGGAGCCAATATTGTCTTTGTGTTCCCGGACATAGTCCAGGAGGCAGCCGAAGGGCATGAGCTGCGTGATGAGCTGCACGGTGGAGGTGAGGCAGATGCCCAGCAGGCGGC Homo sapiens hg19 +EGFR54.chr7.55259514.55259524_tile_1 EGFR54.chr7.55259514.55259524_tile_1 1 chr7 55259486 55259662 + GCTGGCCAAACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAGAAGGAGGCAAAGTAAGGAGGTGGCTTTAGGTCAGCCAGCATTTTCCTGACACCAGGGACCAGGCTGCCTTCCCACTAGC Homo sapiens hg19 +MET1.chr7.116339642.116339642_tile_1 MET1.chr7.116339642.116339642_tile_1 1 chr7 116339614 116339792 + AGCCCAGCCAGTGTCCTGACTGTGTGGTGAGCGCCCTGGGAGCCAAAGTCCTTTCATCTGTAAAGGACCGGTTCATCAACTTCTTTGTAGGCAATACCATAAATTCTTCTTATTTCCCAGATCAT Homo sapiens hg19 +MET2.chr7.116340262.116340262_tile_1 MET2.chr7.116340262.116340262_tile_1 1 chr7 116340234 116340420 + AACAAGATCGTCAACAAAAACAATGTGAGATGTCTCCAGCATTTTTACGGACCCAATCATGAGCACTGCTTTAATAGGGTAAGTCACATCAGTTCCCCACTTATAAACTGTGAGGTATAAATTAGAAATAAGT Homo sapiens hg19 +MET3.chr7.116411990.116411990_tile_1 MET3.chr7.116411990.116411990_tile_1 1 chr7 116411958 116412127 + GCCCAACTACAGAAATGGTTTCAAATGAATCTGTAGACTACCGAGCTACTTTTCCAGAAGGTATATTTCAGTTTATTGTTCTGAGAAATACCTATACATATACCTCAGTGGGTTGT Homo sapiens hg19 +MET4.chr7.116417463.116417464_tile_1 MET4.chr7.116417463.116417464_tile_1 1 chr7 116417431 116417620 + TATATCATGGGACTTTGTTGGACAATGATGGCAAGAAAATTCACTGTGCTGTGAAATCCTTGAACAGTAAGTGGCATTTTATTTAACCATGGAGTATACTTTTGTGGTTTGCAACCTAATAAATAGCTTATAATA Homo sapiens hg19 +MET6.chr7.116423413.116423474_tile_1 MET6.chr7.116423413.116423474_tile_1 1 chr7 116423385 116423555 + TGTATGATAAAGAATACTATAGTGTACACAACAAAACAGGTGCAAAGCTGCCAGTGAAGTGGATGGCTTTGGAAAGTCTGCAAACTCAAAAGTTTACCACCAAGTCAGATGTGGTAAT Homo sapiens hg19 +SMO1.chr7.128845101.128845101_tile_1 SMO1.chr7.128845101.128845101_tile_1 1 chr7 128845073 128845257 + GGTTCGGACAGACAACCCCAAGAGCTGGTACGAGGACGTGGAGGGCTGCGGCATCCAGTGCCAGAACCCGCTCTTCACAGAGGCTGAGCACCAGGACATGCACAGCTACATCGCGGCCTTCGGGGCCGTCACGGGC Homo sapiens hg19 +SMO2.chr7.128846040.128846040_tile_1 SMO2.chr7.128846040.128846040_tile_1 1 chr7 128846010 128846194 + TACGCCCTGATGGCTGGTGTGGTTTGGTTTGTGGTCCTCACCTATGCCTGGCACACTTCCTTCAAAGCCCTGGGCACCACCTACCAGCCTCTCTCGGGCAAGACCTCCTACTTCCACCTGCTCACCTGGTC Homo sapiens hg19 +SMO3.chr7.128846374.128846374_tile_1 SMO3.chr7.128846374.128846374_tile_1 1 chr7 128846348 128846536 + CGTGCTGGCCCCAATCGGCCTGGTGCTCATCGTGGGAGGCTACTTCCTCATCCGAGGTGAGTGAAGACCAGGCCAGGACCAGTTGGGCAACAAAATATACTGGGCACTTGCTGCCAGTACTGGGAGCTGCCAGCACG Homo sapiens hg19 +SMO4.chr7.128850341.128850341_tile_1 SMO4.chr7.128850341.128850341_tile_1 1 chr7 128850311 128850499 + GCACCTGGGTCTGGACCAAGGCCACGCTGCTCATCTGGAGGCGTACCTGGTGCAGGTGGGCATGGCAGCCAGCCCCTCCTGCCCTGCCCGCCTCACCCTCAGCCTTGGGACCCCATCTTTAGGTTTTGTCGGGTCCTG Homo sapiens hg19 +SMO5.chr7.128851593.128851593_tile_1 SMO5.chr7.128851593.128851593_tile_1 1 chr7 128851563 128851734 + GTCACCCCTGTGGCAACTCCAGGTATGAGAGTTCAAGCTTCTGGAGGAAGGTGGGGGGAGCACAGAGGCTGGGGGCTTCTGGGACTGGAGTACAGGGGCTGTCGGAGGAGGAGGAAGAG Homo sapiens hg19 +BRAF1.chr7.140453121.140453193_tile_1 BRAF1.chr7.140453121.140453193_tile_1 1 chr7 140453093 140453267 + CACTCCATCGAGATTTCACTGTAGCTAGACCAAAATCACCTATTTTTACTGTGAGGTCTTCATGAAGAAATATATCTGAGGTGTAGTAAGTAAAGGAAAACAGTAGATCTCATTTTCCTATC Homo sapiens hg19 +BRAF28.chr7.140481397.140481478_tile_1 BRAF28.chr7.140481397.140481478_tile_1 1 chr7 140481369 140481545 + ACTGTTCCAAATGATCCAGATCCAATTCTTTGTCCCACTGTAATCTGCCCATCAGGAATCTCCCAATCATCACTCGAGTCCCGTCTACCAAGTGTTTTCTTGATAAAAACAGTAAAAAAGTCA Homo sapiens hg19 +FGFR1_1.chr8.38282209.38282209_tile_1 FGFR1_1.chr8.38282209.38282209_tile_1 1 chr8 38282183 38282360 + GGGGACCGCTCTGTGGAAGATGGGAGAGGAGGCACTTGTCATGGGGACCTTGCCATGGCTAAAGAGGGGTGGGCTCACCTGCGCCCCACTTGGCTTTCCCAGTGATGGGTTGTAAACCTCCCAGCAC Homo sapiens hg19 +FGFR1_2.chr8.38285938.38285938_tile_1 FGFR1_2.chr8.38285938.38285938_tile_1 1 chr8 38285908 38286090 + TCCGAGGAGGGGAGAGCATCTATGGGAAGAAGAAGGGGCACTGAGGTTCCTCCTAGGGACCCCTAGATTTCACCAAGGCTAGTGCAGTTCCAGATGAACACGGACACCCTCCCCATGGGGATCCCAGTC Homo sapiens hg19 +JAK2_1.chr9.5073769.5073770_tile_1 JAK2_1.chr9.5073769.5073770_tile_1 1 chr9 5073737 5073923 + TATGTGTCTGTGGAGACGAGAGTAAGTAAAACTACAGGCTTTCTAATGCCTTTCTCAGAGCATCTGTTTTTGTTTATATAGAAAATTCAGTTTCAGGATCACAGCTAGGTGTCAGTGTAAACTATAATTT Homo sapiens hg19 +CDKN2A1.chr9.21971153.21971187_tile_1 CDKN2A1.chr9.21971153.21971187_tile_1 1 chr9 21971123 21971308 + GGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGCCAGGGTGGGGGCCGGCATGACGGAAAGGAAGCTTGTGTAGAGCCCCC Homo sapiens hg19 +ABL1_1.chr9.133738330.133738364_tile_1 ABL1_1.chr9.133738330.133738364_tile_1 1 chr9 133738302 133738491 + CCATGAAGCACAAGCTGGGCGGGGGCCAGTACGGGGAGGTGTACGAGGGCGTGTGGAAGAAATACAGCCTGACGGTGGCCGTGAAGACCTTGAAGGTAGGCTGGGACTGCCGGGGGTGCCCAGGGTACGTGGGGCAAG Homo sapiens hg19 +ABL1_9.chr9.133747520.133747520_tile_1 ABL1_9.chr9.133747520.133747520_tile_1 1 chr9 133747476 133747664 + TTTCCTTCTGCAGGAGGACACCATGGAGGTGGAAGAGTTCTTGAAAGAAGCTGCAGTCATGAAAGAGATCAAACACCCTAACCTGGTGCAGCTCCTTGGTGAGTAAGCCCGGGGCTCTGAAGAGAGGGTCTCGCGCCGC Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_1 ABL1_10.chr9.133748283.133748414_tile_1 1 chr9 133748157 133748327 - CCCGTAGGTCATGAACTCAGTGATGATATAGAACGGGGGCTCCCGGGTGCAGACCCCTGCCAACAAGACAACGAGGACTTCAACACGTGGCTCCGCTCCCAACTGAACAAACAACT Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_2 ABL1_10.chr9.133748283.133748414_tile_2 1 chr9 133748277 133748457 + GAACCTCCTGGACTACCTGAGGGAGTGCAACCGGCAGGAGGTGAACGCCGTGGTGCTGCTGTACATGGCCACTCAGATCTCGTCAGCCATGGAGTACCTGGAGAAGAAAAACTTCATCCACAGGTAGGGGCCT Homo sapiens hg19 +ABL1_16.chr9.133750356.133750356_tile_1 ABL1_16.chr9.133750356.133750356_tile_1 1 chr9 133750328 133750516 + GCCCATGCTGGAGCCAAGTTCCCCATCAAATGGACTGCACCCGAGAGCCTGGCCTACAACAAGTTCTCCATCAAGTCCGACGTCTGGGGTAAGGGCTGCTGCTGCACTGAAGTGGTCCTTCCTGACTACAGGAGGGTT Homo sapiens hg19 +NOTCH1_1.chr9.139397768.139397768_tile_1 NOTCH1_1.chr9.139397768.139397768_tile_1 1 chr9 139397740 139397928 + CCAGGTAGACGATGGAGCTGGGCGGACAATCAGAGAGGGGCTGGGACCCGAGGCTTCCTCCTCCCCCGCCCACCGGCCAGGGATGCTGCCGCAGGACACTGAGGCCCATGACGCCACAGTCAGGACATGGTGAGGC Homo sapiens hg19 +NOTCH1_2.chr9.139399344.139399422_tile_1 NOTCH1_2.chr9.139399344.139399422_tile_1 1 chr9 139399316 139399485 + GCAGCACGCGGCTGAGCTCCCGCAGGAAGTGGAAGGAGCTGTTGCGCAGCTGCTCCGGCGGCATCAGCACCACCACCACCAGCGTGCCGGCCGCCAGCCTCTCGGGTACATGCTCCGC Homo sapiens hg19 +RET1.chr10.43609078.43609104_tile_1 RET1.chr10.43609078.43609104_tile_1 1 chr10 43609048 43609226 + CTGCTTCCCTGAGGAGGAGAAGTGCTTCTGCGAGCCCGAAGACATCCAGGGTGAGTGGGTGGCGGCCGGGACCACCACCACCTCCCAGCCCCACAGAGGTCTCAACAGCACATCTGAGGTCCCAACAA Homo sapiens hg19 +RET2_9.chr10.43609940.43609950_tile_1 RET2_9.chr10.43609940.43609950_tile_1 1 chr10 43609902 43610075 - TGGCTTGTGGGCAAACTTGTGGTAGCAGTGGATGCAGAAGGCAGACAGCAGCACCGAGACGATGAAGGAGAAGAGGACAGCGGCTGCGATCACCGTGCGGCACAGCTCGTCGCACAGTGG Homo sapiens hg19 +RET10.chr10.43613840.43613840_tile_1 RET10.chr10.43613840.43613840_tile_1 1 chr10 43613810 43613998 + CGAGTGAGCTGCGAGACCTGCTGTCAGAGTTCAACGTCCTGAAGCAGGTCAACCACCCACATGTCATCAAATTGTATGGGGCCTGCAGCCAGGATGGTAAGGCCAGCTGCAGGGTGAGGTGGGCAGCCACTGCACCCAG Homo sapiens hg19 +RET11_12.chr10.43615567.43615569_tile_1 RET11_12.chr10.43615567.43615569_tile_1 1 chr10 43615533 43615703 + CCTGGTAGCTGAGGGGCGGAAGATGAAGATTTCGGATTTCGGCTTGTCCCGAGATGTTTATGAAGAGGATTCCTACGTGAAGAGGAGCCAGGTGCCCAGTCCCGGGGATGAGGCGGGG Homo sapiens hg19 +RET13.chr10.43617416.43617416_tile_1 RET13.chr10.43617416.43617416_tile_1 1 chr10 43617388 43617564 + ATGGCAATTGAATCCCTTTTTGATCATATCTACACCACGCAAAGTGATGTGTAAGTGTGGGTGTTGCTCTCTTGGGGTGGAGGTTACAGAAACACCCTTATACATGTAGTGGGGCCACGACGC Homo sapiens hg19 +PTEN1.chr10.89624242.89624244_tile_1 PTEN1.chr10.89624242.89624244_tile_1 1 chr10 89624214 89624388 + CAAAGAGATCGTTAGCAGAAACAAAAGGAGATATCAAGAGGATGGATTCGACTTAGACTTGACCTGTATCCATTTCTGCGGCTGCTCCTCTTTACCTTTCTGTCACTCTCTTAGAACGTGG Homo sapiens hg19 +PTEN3.chr10.89685307.89685307_tile_1 PTEN3.chr10.89685307.89685307_tile_1 1 chr10 89685275 89685459 + ATATACAATCTGTAAGTATGTTTTCTTATTTGTATGCTTGCAAATATCTTCTAAAACAACTATTAAGTGAAAGTTATCTGCTTGTTAGAGTGAGGTAGAGTTAAAGATACATTTTAACAGAATTGTATT Homo sapiens hg19 +PTEN4.chr10.89711893.89711900_tile_1 PTEN4.chr10.89711893.89711900_tile_1 1 chr10 89711865 89712039 + GTCAGAGGCGCTATGTGTATTATTATAGCTACCTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN7.chr10.89717615.89717772_tile_1 1 chr10 89717489 89717668 + ATATTGCTGATATTAATCATTAAAATCGTTTTTGACAGTTTGACAGTTAAAGGCATTTCCTGTGAAATAATACTGGTATGTATTTAACCATGCAGATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_2 PTEN7.chr10.89717615.89717772_tile_2 1 chr10 89717615 89717801 - TTTAGCATCTTGTTCTGTTTGTGGAAGAACTCTACTTTGATATCACCACACACAGGTAACGGCTGAGGGAACTCAAAGTACATGAACTTGTCTTCCCGTCGTGTGGGTCCTGAATTGGAGGAATATATCTTCACC Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 1 chr10 89720684 89720870 + CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATCGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_2 PTEN13.chr10.89720716.89720852_tile_2 1 chr10 89720814 89720991 - TTCTTCATCAGCTGTACTCCTAGAATTAAACACACATCACATACATACAAGTCAACAACCCCCACAAAATGTTTAATTTAACTGACCTTAAAATTTGGAGAAAAGTATCGGTTGGCTTT Homo sapiens hg19 +FGFR2_1.chr10.123258034.123258034_tile_1 FGFR2_1.chr10.123258034.123258034_tile_1 1 chr10 123258006 123258184 + GATTTATGATATTCTTGTGTTTCCCAATCATCTTCATCATCTCCATCTCTGACACCAGATCAGAAAGGTCTTTCTCTGTGGCATCATCTATGAACAGTAGGCATATTCACAAATCAGTTCATTTC Homo sapiens hg19 +FGFR2_2.chr10.123274774.123274803_tile_1 FGFR2_2.chr10.123274774.123274803_tile_1 1 chr10 123274746 123274930 + CAGTAAATGGCTATCTCCAGGTAGTCTGGGGAAGCTGTAATCTCCTTTTCTCTTCCAGGCGCTAGATTGCAGATCACAGGAGGAGGAACAGATAAGCAGGCCATAGAGTTAGCACACCAGACTGACGCATC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_1 FGFR2_5.chr10.123279503.123279677_tile_1 1 chr10 123279385 123279555 + AACAGGAAATCAAAGAACCTGTGGCCAAACCCATGAAGGAGACCCCAGTTGTGGGTACCTTTAGATTCAGAAAGTCCTCACCTTGAGAACCTTGAGGTAGGGCAGCCCGTCGGGCCC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_2 FGFR2_5.chr10.123279503.123279677_tile_2 1 chr10 123279471 123279640 - ACGTAGAGTTTGTCTGCAAGGTTTACAGTGATGCCCAGCCCCACATCCAGTGGATCAAGCACGTGGAAAAGAACGGCAGTAAATACGGGCCCGACGGGCTGCCCTACCTCAAGGTT Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_3 FGFR2_5.chr10.123279503.123279677_tile_3 1 chr10 123279587 123279769 + TCTCCTCCGACCACTGTGGAGGCATTTGCCGGCAGTCCGGCTTGGAGGATGGGCCGGTGAGGCGATCGCTCTGGTGGAGAGAGGGAAGAAAGGAGGAGTGGGGATGGGAGAATGAGAGACCAATAAATA Homo sapiens hg19 +HRAS1.chr11.533873.533875_tile_1 HRAS1.chr11.533873.533875_tile_1 1 chr11 533843 534021 + CCTCCTGGCCGGCGGTATCCAGGATGTCCAACAGGCACGTCTCCCCATCAATGACCACCTGCTTCCGGTAGGAATCCTGCAGGAGGACAGGGCTCAGGGACCCCCTCAGGACCTTCCGTGGGGGGA Homo sapiens hg19 +HRAS6.chr11.534285.534289_tile_1 HRAS6.chr11.534285.534289_tile_1 1 chr11 534251 534434 + GCCCACACCGCCGGCGCCCACCACCACCAGCTTATATTCCGTCATCGCTCCTCAGGGGCCTGCGGCCCGGGGTCCTCCTACAGGGTCTCCTGCCCCACCTGCCAAGGAGGGCCCTGCTCAGCCAGGCCCAGGC Homo sapiens hg19 +ATM1.chr11.108117847.108117848_tile_1 ATM1.chr11.108117847.108117848_tile_1 1 chr11 108117817 108117989 + TGTCACCAGGTACAGTAAGTAGGTCATGTCACATTTAGAAATTTCCTGTTAATTTTTTTTTTAAACTGGGCATTTTGGGCTTTTAAAACCTGTGTTCTCACAAAAAGCCTATAAAAT Homo sapiens hg19 +ATM2.chr11.108119823.108119823_tile_1 ATM2.chr11.108119823.108119823_tile_1 1 chr11 108119793 108119963 + TTGTGCCTTGGTAAAGTGTTACCATTTTCTCATTCAGTGTCATTTTAATCTCTTGTATGTTATTTTTCAGAAAACTTTCAGTGGAATCCTTTCATCTCAACCAGAACTAAGTCATTT Homo sapiens hg19 +ATM3.chr11.108123551.108123551_tile_1 ATM3.chr11.108123551.108123551_tile_1 1 chr11 108123513 108123683 + AGTAATTTTCCTCATCTTGTACTGGAGAAAATTCTTGTGAGTCTCACTATGAAAAACTGTAAAGCTGCAATGAATTTTTTCCAAAGCGTGCCAGAATGGTATGTTATCTAATA Homo sapiens hg19 +ATM4.chr11.108137973.108138003_tile_1 ATM4.chr11.108137973.108138003_tile_1 1 chr11 108137939 108138126 + TAATGGAGGTGGAGGATCAGTCATCCATGAATCTATTTAACGATTACCCTGATAGTAGTGTTAGTGATGCAAACGAACCTGGAGAGAGCCAAAGTACCATAGGTAAATACATATTTACTACTTGGGATT Homo sapiens hg19 +ATM6.chr11.108155132.108155132_tile_1 ATM6.chr11.108155132.108155132_tile_1 1 chr11 108155104 108155281 + GGCACAGCAAAGAGAGACTGCTACCAAGGTCTATGATATGCTTAAAAGTGAAAACTTATTGGGAAAACAGGTATGGCTTCAATTTTTATGTACTTTTCATTCCCTGAATGATATGAGATAT Homo sapiens hg19 +ATM7.chr11.108170476.108170479_tile_1 ATM7.chr11.108170476.108170479_tile_1 1 chr11 108170442 108170618 + GGGTCCTATAGATTTCTCTACCATAGCTATACAACATAGTAAAGATGCATCTTATACCAAGGCCCTTAAGTTATTTGAAGATAAAGAACTTCAGTGGACCTTCATAATGCTGACCTACCTGAA Homo sapiens hg19 +ATM9.chr11.108172421.108172421_tile_1 ATM9.chr11.108172421.108172421_tile_1 1 chr11 108172391 108172571 + TTAGCCACAAAGACTGGACATAGTTTCTGGGAGATTTATAAGATGACAACAGATCCAATGCTGGCCTATCTACAGCCTTTTAGAACATCAAGAAAAAAGGTCTCTTAAGTAATAAATGTTTATTGAA Homo sapiens hg19 +ATM10.chr11.108173640.108173640_tile_1 ATM10.chr11.108173640.108173640_tile_1 1 chr11 108173612 108173801 + AAATCTGTGGATTCCTCTAAGTGAAAATCATGACATTTGGATAAAGACACTGACTTGTGCTTTTTTGGACAGTGGAGGCACAAAATGTGAAATTCTTCAATTATTAAAGCCAATGTGTGAAGTAAGAAGATTAATT Homo sapiens hg19 +ATM11.chr11.108180945.108180945_tile_1 ATM11.chr11.108180945.108180945_tile_1 1 chr11 108180915 108181101 + AAGTTGCCAAGGTAGCTCAGTCTTGTGCTGCTCACTTTACAGCTTTACTCTATGCAGAAATCTATGCAGATAAGAAAAGTATGGATGATCAAGAGAAAAGGTAATGGAATTTAGAATTTTTGGTTTTTAAAA Homo sapiens hg19 +ATM12.chr11.108200958.108200961_tile_1 ATM12.chr11.108200958.108200961_tile_1 1 chr11 108200926 108201096 + TTCAGCGAGAGCTGGAGTTGGATGAATTAGCCCTGCGTGCACTGAAAGAGGATCGTAAACGCTTCTTATGTAAAGCAGTTGAAAATTATATCAACTGCTTATTAAGTGGAGAAGA Homo sapiens hg19 +ATM14.chr11.108204681.108204681_tile_1 ATM14.chr11.108204681.108204681_tile_1 1 chr11 108204651 108204823 + TACTATGGAAATTAAGGTAATTTGCAATTAACTCTTGATTTTTTTTAAACTAAATTTTTTTTATTAGATTGAACCATTTGAAATAGTATTTTTATGTAGGTCAAAATTGGTTAAATA Homo sapiens hg19 +ATM15.chr11.108205769.108205769_tile_1 ATM15.chr11.108205769.108205769_tile_1 1 chr11 108205739 108205928 + AGGTGTAAATTTACCAAAAATAATAGATTGTGTAGGTTCCGATGGCAAGGAGAGGAGACAGCTTGTTAAGGTGAGCCTTCCCTTCTCTGGCTTAGCCCTTAGAGTTTTAGTGATGAAAATTTTTAGTTCATATT Homo sapiens hg19 +ATM16.chr11.108206594.108206594_tile_1 ATM16.chr11.108206594.108206594_tile_1 1 chr11 108206566 108206750 + GATGCTGTCATGCAACAGGTCTTCCAGATGTGTAATACATTACTGCAGAGAAACACGGAAACTAGGAAGAGGAAATTAACTATCTGTACTTATAAGGTAACTATTTGTACTTCTGTTAGTTCACCAAAAAC Homo sapiens hg19 +ATM17.chr11.108218089.108218089_tile_1 ATM17.chr11.108218089.108218089_tile_1 1 chr11 108218061 108218247 + TCTAGGTAAGTAATAAAATCTATGTATCTATTCTTTTTAGTAAATATTTGGTCATCATGGAATGTTGTTTGCCTACCAAGATATTACAAATATAAGAGACAGATAAATTGAAGCAGTAAATATTGGGTTTTTT Homo sapiens hg19 +ATM18.chr11.108225590.108225590_tile_1 ATM18.chr11.108225590.108225590_tile_1 1 chr11 108225562 108225751 + AACCATTGTAGAGGTAAAGTATTTTATAAGGAAGACTTTATTTTTTTTCTTACCAGGTAGACTGTGTATCTCATCAGGAAGTCACTGATGTGAAGAGCACTGCTTCATTTTAACATAGGGGGATGTGGCTGGGCAGC Homo sapiens hg19 +ATM19.chr11.108236086.108236203_tile_1 ATM19.chr11.108236086.108236203_tile_1 1 chr11 108236058 108236241 + ACGTGTCTTAATGAGACTACAAGAGAAACTGAAAGGAGTGGAAGAAGGCACTGTGCTCAGTGTTGGTGGACAAGTGAATTTGCTCATACAGCAGGCCATAGACCCCAAAAATCTCAGCCGACTTTTCCCAG Homo sapiens hg19 +KRAS1.chr12.25378562.25378562_tile_1 KRAS1.chr12.25378562.25378562_tile_1 1 chr12 25378532 25378717 + TTGCTGATGTTTCAATAAAAGGAATTCCATAACTTCTTGCTAAGTCCTGAGCCTGTTTTGTGTCTACTGTTCTAGAAGGCAAATCACATTTATTTCCTACTAGGACCATAGGTACATCTTCAGAGTCCTTA Homo sapiens hg19 +KRAS2.chr12.25380275.25380283_tile_1 KRAS2.chr12.25380275.25380283_tile_1 1 chr12 25380245 25380427 + CCTCTTGACCTGCTGTGTCGAGAATATCCAAGAGACAGGTTTCTCCATCAATTACTACTTGCTTCCTGTAGGAATCCTGAGAAGGGAGAAACACAGTCTGGATTATTACAGTGCACCTTTTACTTCAA Homo sapiens hg19 +KRAS7.chr12.25398255.25398285_tile_1 KRAS7.chr12.25398255.25398285_tile_1 1 chr12 25398225 25398414 + TGTATCGTCAAGGCACTCTTGCCTACGCCACCAGCTCCAACTACCACAAGTTTATATTCAGTCATTTTCAGCAGGCCTTATAATAAAAATAATGAAAATGTGACTATATTAGAACATGTCACACATAAGGTTA Homo sapiens hg19 +PTPN11_1.chr12.112888163.112888211_tile_1 PTPN11_1.chr12.112888163.112888211_tile_1 1 chr12 112888135 112888323 + TGGTGATTACTATGACCTGTATGGAGGGGAGAAATTTGCCACTTTGGCTGAGTTGGTCCAGTATTACATGGAACATCACGGGCAATTAAAAGAGAAGAATGGAGATGTCATTGAGCTTAAATATCCTCTGAACTGT Homo sapiens hg19 +PTPN11_10.chr12.112926884.112926888_tile_1 PTPN11_10.chr12.112926884.112926888_tile_1 1 chr12 112926856 112927032 + GGTCAGGGATGGTCCAGACAGAAGCACAGTACCGATTTATCTATATGGCGGTCCAGCATTATATTGAAACACTACAGCGCAGGATTGAAGAAGAGCAGGTACCAGCCTGAGGGCTGGCATGCGG Homo sapiens hg19 +HNF1A_1.chr12.121431413.121431414_tile_1 HNF1A_1.chr12.121431413.121431414_tile_1 1 chr12 121431385 121431558 + GTGGGGCCCAGCATCCCAGCAGATCCTGTTCCAGGCCTATGAGAGGCAGAAGAACCCTAGCAAGGAGGAGCGAGAGACGCTAGTGGAGGAGTGCAATAGGTACAACGGCGGGCGGGAAACAG Homo sapiens hg19 +HNF1A_3.chr12.121432070.121432070_tile_1 HNF1A_3.chr12.121432070.121432070_tile_1 1 chr12 121432042 121432221 + GCGCAAAGAAGAAGCCTTCCGGCACAAGCTGGCCATGGACACGTACAGCGGGCCCCCCCCAGGGCCAGGCCCGGGACCTGCGCTGCCCGCTCACAGCTCCCCTGGCCTGCCTCCACCTGCCCTCTCCCCC Homo sapiens hg19 +FLT3_1.chr13.28592620.28592653_tile_1 FLT3_1.chr13.28592620.28592653_tile_1 1 chr13 28592590 28592766 + CATAGTTGGAATCACTCATGATATCTCGAGCCAATCCAAAGTCACATATCTTCACCACTTTCCCGTGGGTGACAAGCACGTTCCTGGCGGCCAGGTCTCTGTGAACACACTGTCAAGAATGA Homo sapiens hg19 +FLT3_13.chr13.28602329.28602329_tile_1 FLT3_13.chr13.28602329.28602329_tile_1 1 chr13 28602295 28602464 + GTGTGCACGCCCCCAGCAGGTTCACAATATTCTCGTGGCTTCCCAGCTGGGTCATCATCTTGAGTTCTGACATGAGTGCCTCTCTTTCAGAGCTGTCTGCTTTTTCTGTCAAAGAA Homo sapiens hg19 +FLT3_14.chr13.28608244.28608341_tile_1 FLT3_14.chr13.28608244.28608341_tile_1 1 chr13 28608214 28608402 + ACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCATACCTAAATTGCTTCAGAGATGAAATGATGAGTCA Homo sapiens hg19 +FLT3_22.chr13.28610138.28610138_tile_1 FLT3_22.chr13.28610138.28610138_tile_1 1 chr13 28610098 28610267 - TATAGGAGTGAACCACTATGCCCAGCCAGTGAGCTTATTTCACACGTTCTTTTCTATAGGGAAACCTCAAGTGCTCGCAGAAGCATCGGCAAGTCAGGCGTCCTGTTTCTCGGATGG Homo sapiens hg19 +RB1_1.chr13.48919244.48919244_tile_1 RB1_1.chr13.48919244.48919244_tile_1 1 chr13 48919156 48919336 + ATTTACTTTTTTCTATTCTTTCCTTTGTAGTGTCCATAAATTCTTTAACTTACTAAAAGAAATTGATACCAGTACCAAAGTTGATAATGCTATGTCAAGACTGTTGAAGAAGTATGATGTATTG Homo sapiens hg19 +RB1_2.chr13.48923148.48923148_tile_1 RB1_2.chr13.48923148.48923148_tile_1 1 chr13 48923120 48923296 + TTATTAGCTAAAGGTAAGTTCATTATATTTATTAAATGCTAATATTTCAAATGTAATAATTAAATTGGCATTCCTTTGGACTAAATTCCCCAATTTTTATTGAGTAATGTACTCCTCCCTCAT Homo sapiens hg19 +RB1_3.chr13.48942685.48942685_tile_1 RB1_3.chr13.48942685.48942685_tile_1 1 chr13 48942655 48942826 + ACGAAAAAGTAACCTTGATGAAGAGGTGAATGTAATTCCTCCACACACTCCAGTTAGGTATGAATTTTCCTACTTTTAATTATATTATAATTTTGTTATTCATGGCTTTATAGTG Homo sapiens hg19 +RB1_4.chr13.48955538.48955550_tile_1 RB1_4.chr13.48955538.48955550_tile_1 1 chr13 48955504 48955684 + TAGAACGATGTGAACATCGAATCATGGAATCCCTTGCATGGCTCTCAGTAAGTAGCTAAATAATTGAAGAAATTCATTCATGTGCATATGGCTAACAAATTATTGTTAGTGAGAGGTGTTTCTTA Homo sapiens hg19 +RB1_6.chr13.49027168.49027168_tile_1 RB1_6.chr13.49027168.49027168_tile_1 1 chr13 49027112 49027288 + TTTGATCTTATTAAACAATCAAAGGACCGAGAAGGACCAACTGATCACCTTGAATCTGCTTGTCCTCTTAATCTTCCTCTCCAGAATAATCACACTGCAGCAGATATGTAAGCAAAATATA Homo sapiens hg19 +RB1_7.chr13.49033843.49033846_tile_1 RB1_7.chr13.49033843.49033846_tile_1 1 chr13 49033813 49033989 + TCTCCGGCTAAATACACTTTGTGAACGCCTTCTGTCTGAGCACCCAGAATTAGAACATATCATCTGGACCCTTTTCCAGCACACCCTGCAGAATGAGTATGAACTCATGAGAGACAGGCATTT Homo sapiens hg19 +RB1_8.chr13.49037877.49037877_tile_1 RB1_8.chr13.49037877.49037877_tile_1 1 chr13 49037815 49037985 + TTTACATCAATTTATTTACTAGATTATGATGTGTTCCATGTATGGCATATGCAAAGTGAAGAATATAGACCTTAAATTCAAAATCATTGTAACAGCATACAAGGATCTTCCTCA Homo sapiens hg19 +RB1_9.chr13.49039164.49039164_tile_1 RB1_9.chr13.49039164.49039164_tile_1 1 chr13 49039132 49039304 + AAGAGGAGTATGATTCTATTATAGTATTCTATAACTCGGTCTTCATGCAGAGACTGAAAACAAATATTTTGCAGTATGCTTCCACCAGGGTAGGTCAAAAGTATCCTTTGATTGGAAAA Homo sapiens hg19 +AKT1.chr14.105246455.105246455_tile_1 AKT1.chr14.105246455.105246455_tile_1 1 chr14 105246429 105246600 + CTCACGTTGGTCCACATCCTGCGGCCGCTCCTTGTAGCCAATGAAGGTGCCATCATTCTTGAGGAGGAAGTAGCGTGGCCGCCAGGTCTTGATGTACTCCCCTACAGACGTGCGGGTGGTGA Homo sapiens hg19 +CDH1_1.chr16.68835649.68835650_tile_1 CDH1_1.chr16.68835649.68835650_tile_1 1 chr16 68835613 68835782 + TGGGCACAGATGGTGTGATTACAGTCAAAAGGCCTCTACGGTTTCATAACCCACAGATCCATTTCTTGGTCTACGCCTGGGACTCCACCTACAGAAAGTTTTCCACCAAAGTCACGCTGAAT Homo sapiens hg19 +CDH1_2.chr16.68846137.68846137_tile_1 CDH1_2.chr16.68846137.68846137_tile_1 1 chr16 68846109 68846283 + CGATAATCCTCCGATCTTCAATCCCACCACGGTAATTCTATAACTCCTTAGAGGGTTTCCAAAGAAAGGTCTTTTGTTGTTCATGAACTAAGTGTCACCACTGCTCATGGGCGAAGTCTTT Homo sapiens hg19 +CDH1_3.chr16.68847274.68847277_tile_1 CDH1_3.chr16.68847274.68847277_tile_1 1 chr16 68847246 68847422 + ACTGATGCTGATGCCCCCAATACCCCAGCGTGGGAGGCTGTATACACCATATTGAATGATGATGGTGGACAATTTGTCGTCACCACAAATCCAGTGAACAACGATGGCATTTTGAAAACAGCA Homo sapiens hg19 +TP53_1.chr17.7574003.7574021_tile_1 TP53_1.chr17.7574003.7574021_tile_1 1 chr17 7573977 7574147 + CGGAACATCTCGAAGCGCTCACGCCCACGGATCTGCAGCAACAGAGGAGGGGGAGAAGTAAGTATATACACAGTACCTGAGTTAAAAGATGGTTCAAGTTACAATTGTTTGACTTTATG Homo sapiens hg19 +TP53_3.chr17.7577022.7577129_tile_1 TP53_3.chr17.7577022.7577129_tile_1 1 chr17 7576996 7577166 + CGCTTAGTGCTCCCTGGGGGCAGCTCGTGGTGAGGCTCCCCTTTCTTGCGGAGATTCTCTTCCTCTGTGCGCCGGTCTCTCCCAGGACAGGCACAAACACGCACCTCAAAGCTGTTCCG Homo sapiens hg19 +TP53_17.chr17.7577523.7577574_tile_1 TP53_17.chr17.7577523.7577574_tile_1 1 chr17 7577495 7577683 + GGTGAGGATGGGCCTCCGGTTCATGCCGCCCATGCAGGAACTGTTACACATGTAGTTGTAGTGGATGGTGGTACAGTCAGAGCCAACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_1 TP53_31_59.chr17.7578190.7578536_tile_1 1 chr17 7578064 7578234 + AGAAAGCCCCCCTACTGCTCACCTGGAGGGCCACTGACAACCACCCTTAACCCCTCCTCCCAGAGACCCCAGTTGCAAACCAGACCTCAGGCGGCTCATAGGGCACCACCACACTA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_2 TP53_31_59.chr17.7578190.7578536_tile_2 1 chr17 7578156 7578325 - CTGATTGCTCTTAGGTCTGGCCCCTCCTCAGCATCTTATCCGAGTGGAAGGAAATTTGCGTGTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCC Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_3 TP53_31_59.chr17.7578190.7578536_tile_3 1 chr17 7578246 7578415 + TGAGGAGGGGCCAGACCTAAGAGCAATCAGTGAGGAATCAGAGGCCTGGGGACCCTGGGCAACCAGCCCTGTCGTCTCTCCAGCCCCAGCTGCTCACCATCGCTATCTGAGCAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_4 TP53_31_59.chr17.7578190.7578536_tile_4 1 chr17 7578346 7578515 - GTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAGTCACAGCACATGACGGAGGTTGTGAGGCGCTGCCCCCACCATGAGCGCTGCTCAGATAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_5 TP53_31_59.chr17.7578190.7578536_tile_5 1 chr17 7578468 7578645 + CCCACAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTAGGAAGAGGAAGGAGACAGAGTTGAAAGTCAGGGCACAAGTGAACAGATAAAGCAACTGGA Homo sapiens hg19 +TP53_60.chr17.7579358.7579403_tile_1 TP53_60.chr17.7579358.7579403_tile_1 1 chr17 7579324 7579507 + GCCCAGACGGAAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGGACAGAAGATGACAGGGGCCAGGAGGGGGCTGGTGCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGCAGGGGCCACGGGGGGAGCAG Homo sapiens hg19 +TP53_64.chr17.7579882.7579882_tile_1 TP53_64.chr17.7579882.7579882_tile_1 1 chr17 7579852 7580032 + GCTCGACGCTAGGATCTGACTGCGGCTCCTCCATGGCAGTGACCCGGAAGGCAGTCTGGCTGCTGCAAGAGGAAAAGTGGGGATCCAGCATGAGACACTTCCAACCCTGGGTCACCTGGGCCTGCAG Homo sapiens hg19 +ERBB2_1.chr17.37880219.37880261_tile_1 ERBB2_1.chr17.37880219.37880261_tile_1 1 chr17 37880191 37880361 + TGTTGAGGGAAAACACATCCCCCAAAGCCAACAAAGAAATCTTAGACGTAAGCCCCTCCACCCTCTCCTGCTAGGAGGACAGGAAGGACCCCATGGCTGCAGGTCTGGGCTCTGGTCT Homo sapiens hg19 +ERBB2_4.chr17.37880993.37881012_tile_1 ERBB2_4.chr17.37880993.37881012_tile_1 1 chr17 37880963 37881151 + CGTGATGGCTGGTGTGGGCTCCCCATATGTCTCCCGCCTTCTGGGCATCTGCCTGACATCCACGGTGCAGCTGGTGACACAGCTTATGCCCTATGGCTGCCTCTTAGACCATGTCCGGGAAAACCGCGGACGCCTGGG Homo sapiens hg19 +ERBB2_13.chr17.37881332.37881440_tile_1 ERBB2_13.chr17.37881332.37881440_tile_1 1 chr17 37881298 37881482 + GCGGCTCGTACACAGGGACTTGGCCGCTCGGAACGTGCTGGTCAAGAGTCCCAACCATGTCAAAATTACAGACTTCGGGCTGGCTCGGCTGCTGGACATTGACGAGACAGAGTACCATGCAGATGGGGGCA Homo sapiens hg19 +SMAD4_1.chr18.48575169.48575170_tile_1 SMAD4_1.chr18.48575169.48575170_tile_1 1 chr18 48575131 48575301 + TTTGACTTAAAATGTGATAGTGTCTGTGTGAATCCATATCACTACGAACGAGTTGTATCACCTGGAATTGGTAAGTAGACTTTGCTTTCATCCTAAGAAACATAAAGGGAAA Homo sapiens hg19 +SMAD4_2.chr18.48581198.48581198_tile_1 SMAD4_2.chr18.48581198.48581198_tile_1 1 chr18 48581168 48581346 + AGGGACAGCCATCGTTGTCCACTGAAGGACATTCAATTCAAACCATCCAGCATCCACCAAGTAATCGTGCATCGACAGAGACATACAGCACCCCAGCTCTGTTAGCCCCATCTGAGTCTAATGC Homo sapiens hg19 +SMAD4_3.chr18.48584560.48584560_tile_1 SMAD4_3.chr18.48584560.48584560_tile_1 1 chr18 48584528 48584714 + GGGCCTCAGCCAGGACAGCAGCAGAATGGATTTACTGGTCAGCCAGCTACTTACCATCATAGTATGTACATACTTTAAAAAATCTTTTAAATAGTTGAGAAAAAAGTAGGCAGCCTTTATAAAAGCAAATTAAC Homo sapiens hg19 +SMAD4_4.chr18.48586262.48586262_tile_1 SMAD4_4.chr18.48586262.48586262_tile_1 1 chr18 48586234 48586416 + CCAGCCTCCCATTTCCAATCATCCTGGTAAGTGTATTTCAAAATTGATTTCCTGTATTTAGATTGATTTAGTGGTGATTGAAACGCACAAACACAGGCTTTAATGGAATTATGGGGTCACTTCTCAGAT Homo sapiens hg19 +SMAD4_5.chr18.48591826.48591919_tile_1 SMAD4_5.chr18.48591826.48591919_tile_1 1 chr18 48591796 48591982 + TTGAAATGGATGTTCAGGTAGGAGAGACATTTAAGGTTCCTTCAAGCTGCCCTATTGTTACTGTTGATGGATACGTGGACCCTTCTGGAGGAGATCGCTTTTGTTTGGGTCAACTCTCCAATGTCCACAGGAC Homo sapiens hg19 +SMAD4_11.chr18.48593405.48593405_tile_1 SMAD4_11.chr18.48593405.48593405_tile_1 1 chr18 48593377 48593547 + AAGGTGTGCAGTTGGAATGTAAAGGTGAAGGTGATGTTTGGGTCAGGTGCCTTAGTGACCACGCGGTCTTTGTACAGAGTTACTACTTAGACAGAGAAGCTGGGCGTGCACCTGGAGA Homo sapiens hg19 +SMAD4_12.chr18.48603032.48603094_tile_1 SMAD4_12.chr18.48603032.48603094_tile_1 1 chr18 48602998 48603168 + TGTCATCGACAGATGCAGCAGCAGGCGGCTACTGCACAAGCTGCAGCAGCTGCCCAGGCAGCAGCCGTGGCAGGAAACATCCCTGGCCCAGGATCAGTAGGTGGAATAGCTCCA Homo sapiens hg19 +SMAD4_15.chr18.48604668.48604754_tile_1 SMAD4_15.chr18.48604668.48604754_tile_1 1 chr18 48604638 48604808 + CGTCGCTTATGCATACTCAGGATGAGTTTTGTGAAAGGCTGGGGACCGGATTACCCAAGACAGAGCATCAAAGAAACACCTTGCTGGATTGAAATTCACTTACACCGGGCCCTCCAGC Homo sapiens hg19 +STK11_1.chr19.1207021.1207092_tile_1 STK11_1.chr19.1207021.1207092_tile_1 1 chr19 1206993 1207169 + CCAGCCGCGCCGCAAGCGGGCCAAGCTCATCGGCAAGTACCTGATGGGGGACCTGCTGGGGGAAGGCTCTTACGGCAAGGTGAAGGAGGTGCTGGACTCGGAGACGCTGTGCAGGAGGGCCGT Homo sapiens hg19 +STK11_4.chr19.1220487.1220502_tile_1 STK11_4.chr19.1220487.1220502_tile_1 1 chr19 1220459 1220638 + CCGACCTGGGCGTGGCCGAGGTAGGCACGTGCTAGGGGGGGCCCTGGGGCGCCCCCTCCCGGGCACTCCCTGAGGGCTGCACGGCACCGCCACAGGCACTGCACCCGTTCGCGGCGGACGACACCTGCCG Homo sapiens hg19 +STK11_8.chr19.1221264.1221319_tile_1 STK11_8.chr19.1221264.1221319_tile_1 1 chr19 1221232 1221407 - CCCGCCTCCCTGGGGCTGCGGGCAGAGGGATGAGGCTCCCACCTTTCAGCAGGTCAGAGAGCGGGGGGCCACAGTCGCCCGGGATGGCGTAGCTCCCCTTCCCGATGTTCTCAAACAACTTG Homo sapiens hg19 +STK11_12.chr19.1223059.1223125_tile_1 STK11_12.chr19.1223059.1223125_tile_1 1 chr19 1223035 1223221 + GGCGCAGCATGACTGTGGTGCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACATCATCTACACTCAGGACTTCACGGTGCCCGGTGAGTCTGGCGGGGGCCCCTGCCC Homo sapiens hg19 +JAK3_1.chr19.17945696.17945696_tile_1 JAK3_1.chr19.17945696.17945696_tile_1 1 chr19 17945666 17945840 + GGTGACGCCACTAAACACTTCCCAGACCGTGGCGCCGAAGCCCCACTTGTCAGCTTCCAAGCTAAGTGTCTGCGCCTCCCGGAGACACTCGGGGGCCACCCAGGGGATCCTGTCGGTGAGCAC Homo sapiens hg19 +JAK3_2.chr19.17948009.17948009_tile_1 JAK3_2.chr19.17948009.17948009_tile_1 1 chr19 17947981 17948169 + CGCTGCTTCCAGGAATGACTGGGGAAGGTGGGAAGGGAGAGAAGATGCGTGGGTTTCTTCCACTCCAATAATCCCAAATTTTGTGCTCACAGACCTGCCTTAGGGGAACACCTGGCCACAGGTCACCTTTGGCCCTGG Homo sapiens hg19 +SRC.chr20.36031762.36031762_tile_1 SRC.chr20.36031762.36031762_tile_1 1 chr20 36031734 36031923 + CCAGCCCGGGGAGAACCTCTAGGCACAGGCGGGCCCAGACCGGCTTCTCGGCTTGGATCCTGGGCTGGGTGGCCCCTGTCTCGGGGCTTGCCCCACTCTGCCTGCCTGCTGTTGGTCCTCTCTCTGTGGGGCTGA Homo sapiens hg19 +GNAS1.chr20.57484420.57484421_tile_1 GNAS1.chr20.57484420.57484421_tile_1 1 chr20 57484390 57484560 + TGCCGTGTCCTGACTTCTGGAATCTTTGAGACCAAGTTCCAGGTGGACAAAGTCAACTTCCAGTAAGCCAACTGTTACCTTTTTATATAACAGAGATCATGGTTTCTTGACATTCAC Homo sapiens hg19 +SMARCB1_1.chr22.24133967.24133990_tile_1 SMARCB1_1.chr22.24133967.24133990_tile_1 1 chr22 24133939 24134126 + TCCGAGGTTCTCTGTACAAGAGATACCCCTCACTCTGGAGGCGACTAGCCACTGTGGAAGAGAGGAAGAAAATAGTTGCATCGTCACATGGTAAAAAAACAAAACCTAACACTAAGGGTGCGTCTTCACGAGGGTT Homo sapiens hg19 +SMARCB1_3.chr22.24143240.24143240_tile_1 SMARCB1_3.chr22.24143240.24143240_tile_1 1 chr22 24143210 24143383 + GGGCCGAGACAAGAAGAGAACCTTCCCCCTTTGGTGTGGATGCATCGCTGCACTCACCCTCCGTGCTGATTCCGCCTTAGTTCTCCAGCACGTTTCAGTTCCTTCCTCCCCAGAAAAACACT Homo sapiens hg19 +SMARCB1_4.chr22.24145582.24145582_tile_1 SMARCB1_4.chr22.24145582.24145582_tile_1 1 chr22 24145552 24145726 + GCTGCGAGACGCCTTCACCTGGAACATGAATGGTACAAGGCAGTCGGGCTTGGCTGGGCCTGGCCCCAACCCCTGTGTGTTACGTGGGAACAGTCCCGTTTCCTGCCAGCTGCCTGTCAGGC Homo sapiens hg19 +SMARCB1_5_6.chr22.24176352.24176357_tile_1 SMARCB1_5_6.chr22.24176352.24176357_tile_1 1 chr22 24176324 24176495 + CGGCCCCGGCCTGGTAACCAGCCCATCAGCACACGGCTCCCACGGAGCATCTCAGAAGATTGGGCCGCCTCTCCTCCATCTTCTGGCAAGGACAGAGGCGAGGGGACAGCCCAGCGCCA Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_1 GNA11_4.chr19.3114942.3115070_tile_1 1 chr19 3114824 3115004 - GTAGCCCAAGGTGGCGATGCGGTCAACGTCGGTCAGGTAGCTGCAACACAGCGGTGGGTGCTCAGGCCGGCTGCCGGGGGTGGGGGGGCAGGACAGGGACACAGCACCCAAACCAGCGGGAGGACGGAAAGCCACC Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_2 GNA11_4.chr19.3114942.3115070_tile_2 1 chr19 3114958 3115133 + CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCATCATCGAGTACCCTTTCGACCTGGAGAACATCATCTTCCGGTACCGCCCGGGCCACAGCAGGCGGGGAGGGGGCACTGAGA Homo sapiens hg19 +GNA11_5.chr19.3118922.3119051_tile_1 GNA11_5.chr19.3118922.3119051_tile_1 1 chr19 3118802 3118989 - CACTTCCTCCGCTCCGACCGCTGGCCCCCCACATCCACCATCCTGAAAGGACACAGCGCCAGGACTCAGCCACCTGGCGCCCCAAGGCCCAATCTGCAATCCCAGGACGGCTCCCACCCAAGCCCCTCCTGCCACACC Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_6.chr19.3119204.3119357_tile_2 1 chr19 3119208 3119395 - CCGCAGCCCGGCGCACCATCGAACTCGGGGAAGTAGTCCACCAGGTGCGAGTACAGGATCTTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGAGGATGACGGAGGAGTTCTGGAACCAGGGGTAGGTGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_7.chr19.3120987.3121177_tile_1 1 chr19 3120865 3121035 + GGGCCTTACTCGCTCATCCCCTGGGAGTGACAAAGGGGCCCACGAGTCCCTTGCCCTGGGCCGGGCTGGGGCACAGCCTCACCCTCTGCCCTCCCCCAGGTCCCCAGCGGGACGCCCAGGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 1 chr19 3120985 3121170 - CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTCCGTGTCGGTGGCACACGTGAAGTGTGAGTAGATGATCTTGTCGCTGTCGGGGTTCAGGTCCACGAACATCTTCAGGATGAACTCCCGCGCCGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_3 GNA11_7.chr19.3120987.3121177_tile_3 1 chr19 3121121 3121304 + GCAGCTCAACCTCAAGGAGTACAACCTGGTCTGAGCGCCCAGGCCCAGGGAGACGGGATGGAGACACGGGGCAGGACCTTCCTTCCACGGAGCCTGCGGCTGCCGGGCGGGTGGCGCTGCCGAGTCCGGGCCGGGGC Homo sapiens hg19 +GNAQ_4.chr9.80412436.80412564_tile_1 GNAQ_4.chr9.80412436.80412564_tile_1 1 chr9 80412406 80412592 + TACCTGAAAATGACACTTTGTAAGTCAAAGGGGTATTCGATGATCCCTGTGGTGGGGACTCGAACTCTAAGCACATCTTGTTGCGTAGGCAGGTAGGCAGGGTCAGCTACGCGGTCCAAGTCATTAAGATAGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_5.chr9.80409379.80409508_tile_1 1 chr9 80409249 80409421 + AAAGAAGTAAGTTCACTCCATTCCCCACACCCTACTTTCTATCATTTACTTGTATCAGATAATAAAATGATAATCCATTGCCTGTCTAAAGAACACTTACCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 1 chr9 80409335 80409510 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCAAGTTCTCGTGGAGTCAGACAATGAGGTAAGTGTTCTTTA Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_3 GNAQ_5.chr9.80409379.80409508_tile_3 1 chr9 80409459 80409639 + TTTGGCCCCCTACATCGACCATTCTGCAAGGTTAACAATACTCATATTAATAACATATAAAGTAAAACTAAAAAGTCAACATAAATATAGCACTACTTACAAACTTAGGGAAAATATTCTCTTGAAT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_6.chr9.80343430.80343583_tile_1 1 chr9 80343306 80343476 + GGGCAGCAATGGTGCACTGTAGTGCGTTAACTCCCACACTGGGGTTTGGAGACAAAACCTATTCACAGCTACTGAGCTGTGGTATGAGTGCTGACTTACCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_2 GNAQ_6.chr9.80343430.80343583_tile_2 1 chr9 80343392 80343561 - GGTTCCAGAACTCCTCGGTTATTCTGTTCTTAAACAAGAAAGATCTTCTAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGTAAGTCAGCAC Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_3 GNAQ_6.chr9.80343430.80343583_tile_3 1 chr9 80343504 80343689 + CAGGGGTATGTGATAATTGTTCTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTGGAAAAAAAAAAAAAATCAGAAAAAACAAGGAGTGAATTACATGATTACTTAATTTGTGAATTGTGTTTATTTT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 1 chr9 80336110 80336280 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCAGGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAATTAGACCAGATTGTACT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_7.chr9.80336240.80336429_tile_2 1 chr9 80336204 80336374 - CTACTCCCACTTCACGTGCGCCACAGACACCGAGAATATCCGCTTTGTCTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGAGTACAATCTGGTCTAATTGTGCCTCC Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_3 GNAQ_7.chr9.80336240.80336429_tile_3 1 chr9 80336320 80336495 + GATAATTTTGTCACTGTCTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCTTTCGGCCAAGAGACAAGAGGGACACTTTGTTACCTA Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 2 chr22 17052964 17053133 + ATCCTCTCTCTGAAATCACTGCGCAGGAGAAAGATTTTCTATGGACCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGACTTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 2 chr22 17055413 17055585 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTGTCAAACAGGAGAAGAAGGATGAAACACAAAAGTTGTGTGACTCTAGTCTGTGTTTGAGACTCTT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN3.chr10.89685307.89685307_tile_1 2 chr9 33675957 33676480 - ATACACAATCTTTGTGCTGAAAGACATTATGACACCGCCAAATCTAATTACAGAGTTGCGCAATATCCTTTTGAAGACCATAACCCACCACAGCTAGAACTTATCAAACCCTTTTGTGAAGATCTTGACCAATGGCTAAGTGAAGATGACAATCATGTTGCAGCAATTCACTGTAAAGCTGGAAAGGGACGAACTGGTATAATGATTTATGCATATTTATTACATCGGGGCAAATTTTTAAAGGCACAAGAGGCCCTAGATTTCTATGGGGAAGTAAGGACCAGAGACAAAAAGGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTACTATAGCTACCTGGTAAAGAATCATGTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 2 chr9 33675629 33675815 - CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATTGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAGTATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 2 chr7 65970150 65970483 + CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTTCGTGTCGGTGGCGTACGTGAAGTGGGAGTCGATGATCTTGTCGCTGTCGGGGTTCATGTCCACTAACATCTTCAGGATGAACTCCCGCGCCGCCTGGGCGTCCTGCTGGGGCCCTTCGAACTCGGGGAAGTAGTCCACCATGTGTGAGTACAGGATATTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGGTGATGACGGGGGAGTTCTGGAACCAGGGGTAGTCGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_4.chr19.3114942.3115070_tile_2 2 chr7 65970285 65970719 - CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCGTCTTTCGACCTGGAGAACATCATCTTCAGGATGGCGGATGTTGGGGGACAGCGGTCGGCGCAGAGGAAGTGGATCCACTGCTTTGAGAACCTGACGTCCATCCCGTTTCTCGTCGCCCTCAGTGAATACGACCAAGTCCTGGTGGAGTCGGACAACGAGAACCGGATGGAGGAGAGCAAAGCCCTGTTCCGGACCATCATCGACTACCCCTGGTTCCAGAACTCCCCCGTCATCACCTTCCTCAACAAGAAGGACCTGCTGGAGGACAATATCCTGTACTCACACATGGTGGACTACTTCCCCGAGTTCGAAGGGCCCCAGCAGGACGCCCAGGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 2 chr2 132181238 132181750 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCATGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAACTAGACCAGATTGTAATCCTTCAGGTTCAACTGGAGGATGGTGTCCTTGACGGCAGCAAACACAAAGCGGATATTCTCGGTGTCTGTGGCGCATGTGAAGTGGGAGTAGATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGTAGTCGACTAGATGGGAATACATGATTTTCTCCTCTGGAAGATCTTTCTTGTTTAACAACAGAATAACCGAGGAGTTCTGGAACCAGGGATACGTGATAATTGTACTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_7.chr9.80336240.80336429_tile_3 2 chr2 132181448 132181600 + GATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 2 chr2 132181332 132181839 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCGAGTTCTCGTGGAGTCAGACAATGAGAACCGAATGGAGGAAAGCAAGGCTCTCTTTAGTACAATTATCACGTATCCCTGGTTCCAGAACTCCTCGGTTATTCTGTTGTTAAACAAGAAAGATCTTCCAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGACCCCAGAGAGATGCCCAGGCAGCCCGAGAATTCATTCTGAAGATGTTCGTGGACCTGAACCCAGTGACCAAATTATCTACTCCCACTTCACATGCGCCACAGACACCGAGAATATCCGCTTTGTGTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGATTACAATCTGGTCTAGTTGTGCCTCC Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 2 chr2 132181238 132181408 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCATGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAACTAGACCAGATTGTAAT Homo sapiens hg19 +IDH1_1_2.chr2.209113112.209113113_tile_1 IDH1_1_2.chr2.209113112.209113113_tile_1 2 chr6 7517651 7517831 + GCGACCTACGATGATGGATTTTACCCATCCACTCACAAGCTGGGGGATATTTTTGCAGATAATGGCTTCTCTGAGGACCGTGCCAACCAGAATATTTTGGATGGTGCCATTTGGCGATTTCCACATT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN4.chr10.89711893.89711900_tile_1 2 chr9 33675957 33676167 - GTCAGAGGCGCTATGTGTATTACTATAGCTACCTGGTAAAGAATCATGTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN4.chr10.89711893.89711900_tile_1 2 chr9 33675629 33676167 - GTCAGAGGCGCTATGTGTATTACTATAGCTACCTGGTAAAGAATCATGTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAGGTGAAGATGTATTCCTCCAATTCAGGACCCACACGATGGGAGGACAAGTTCATGTATTTTGAGTTCCCTCAGCCGTTACCTGTGTGTGGTGATATCAAAGTAGAGTTCTTCCACAAACAGAACAAGATGCTAAAAAAGGACAAAATGTTTCACTTTTGGGTAAATACATTCTTCATACCAGGACCAGAGGAAACCTCAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATTGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAGTATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/filters/CosmicCodingMuts_v64_26032013_noLimit_wgs.f.vcf Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,3210 @@ +##fileformat=VCFv4.1 +##source=COSMICv64 +##reference=GRCh37 +##fileDate=20130327 +##comment="Missing nucleotide details indicate ambiguity during curation process" +##comment="URL stub for COSM ID field='http://www.sanger.ac.uk/cgi-bin/genetics/CGP/directive?id='" +##comment="REF and ALT sequences are both forward strand +##INFO=<ID=GENE,Number=1,Type=String,Description="Gene name"> +##INFO=<ID=STRAND,Number=1,Type=String,Description="Gene strand"> +##INFO=<ID=CDS,Number=1,Type=String,Description="CDS annotation"> +##INFO=<ID=AA,Number=1,Type=String,Description="Peptide annotation"> +##INFO=<ID=CNT,Number=1,Type=Integer,Description="How many samples have this mutation"> +#CHROM POS ID REF ALT QUAL FILTER INFO +1 115256508 COSM43344 C G . . GENE=NRAS;STRAND=-;CDS=c.203G>C;AA=p.R68T;CNT=1 +1 115256528 COSM586 T G . . GENE=NRAS;STRAND=-;CDS=c.183A>C;AA=p.Q61H;CNT=3 +1 115256528 COSM585 T A . . GENE=NRAS;STRAND=-;CDS=c.183A>T;AA=p.Q61H;CNT=4 +1 115256529 COSM582 T G . . GENE=NRAS;STRAND=-;CDS=c.182A>C;AA=p.Q61P;CNT=2 +1 115256529 COSM583 T A . . GENE=NRAS;STRAND=-;CDS=c.182A>T;AA=p.Q61L;CNT=9 +1 115256529 COSM584 T C . . GENE=NRAS;STRAND=-;CDS=c.182A>G;AA=p.Q61R;CNT=25 +1 115256529 COSM221918 TGT TTG . . GENE=NRAS;STRAND=-;CDS=c.180_181AC>CA;AA=p.G60>?;CNT=1 +1 115256530 COSM580 G T . . GENE=NRAS;STRAND=-;CDS=c.181C>A;AA=p.Q61K;CNT=22 +1 115256562 COSM222543 G A . . GENE=NRAS;STRAND=-;CDS=c.149C>T;AA=p.T50I;CNT=2 +1 115256591 COSM675199 G T . . GENE=NRAS;STRAND=-;CDS=c.120C>A;AA=p.Y40*;CNT=1 +1 115258712 COSM212982 T G . . GENE=NRAS;STRAND=-;CDS=c.70A>C;AA=p.I24L;CNT=1 +1 115258718 COSM1167956 G T . . GENE=NRAS;STRAND=-;CDS=c.64C>A;AA=p.Q22K;CNT=1 +1 115258744 COSM574 C A . . GENE=NRAS;STRAND=-;CDS=c.38G>T;AA=p.G13V;CNT=1 +1 115258744 COSM573 C T . . GENE=NRAS;STRAND=-;CDS=c.38G>A;AA=p.G13D;CNT=3 +1 115258745 COSM569 C G . . GENE=NRAS;STRAND=-;CDS=c.37G>C;AA=p.G13R;CNT=3 +1 115258747 COSM564 C T . . GENE=NRAS;STRAND=-;CDS=c.35G>A;AA=p.G12D;CNT=9 +1 115258747 COSM566 C A . . GENE=NRAS;STRAND=-;CDS=c.35G>T;AA=p.G12V;CNT=1 +1 115258747 COSM565 C G . . GENE=NRAS;STRAND=-;CDS=c.35G>C;AA=p.G12A;CNT=2 +1 115258748 COSM562 C A . . GENE=NRAS;STRAND=-;CDS=c.34G>T;AA=p.G12C;CNT=5 +1 115258748 COSM563 C T . . GENE=NRAS;STRAND=-;CDS=c.34G>A;AA=p.G12S;CNT=2 +10 43609932 COSM538678 A G . . GENE=RET;STRAND=+;CDS=c.1884A>G;AA=p.P628P;CNT=1 +10 43609955 COSM72408 C T . . GENE=RET;STRAND=+;CDS=c.1907C>T;AA=p.T636M;CNT=1 +10 43609990 COSM1223553 G A . . GENE=RET;STRAND=+;CDS=c.1942G>A;AA=p.V648I;CNT=1 +10 43609995 COSM343849 G T . . GENE=RET;STRAND=+;CDS=c.1947G>T;AA=p.S649S;CNT=1 +10 43610062 COSM918117 G T . . GENE=RET;STRAND=+;CDS=c.2014G>T;AA=p.A672S;CNT=1 +10 43613825 COSM918121 C T . . GENE=RET;STRAND=+;CDS=c.2289C>T;AA=p.N763N;CNT=1 +10 43613844 COSM272178 C T . . GENE=RET;STRAND=+;CDS=c.2308C>T;AA=p.R770*;CNT=1 +10 43613905 COSM343401 T A . . GENE=RET;STRAND=+;CDS=c.2369T>A;AA=p.L790*;CNT=1 +10 43613908 COSM1159820 A T . . GENE=RET;STRAND=+;CDS=c.2372A>T;AA=p.Y791F;CNT=1 +10 43615538 COSM225294 C T . . GENE=RET;STRAND=+;CDS=c.2617C>T;AA=p.R873W;CNT=2 +10 43615593 COSM538676 C A . . GENE=RET;STRAND=+;CDS=c.2672C>A;AA=p.S891*;CNT=1 +10 43617398 COSM188545 G T . . GENE=RET;STRAND=+;CDS=c.2735G>T;AA=p.R912L;CNT=1 +10 89624234 COSM87309 C A . . GENE=PTEN;STRAND=+;CDS=c.8C>A;AA=p.A3D;CNT=1 +10 89624245 COSM5298 G T . . GENE=PTEN;STRAND=+;CDS=c.19G>T;AA=p.E7*;CNT=1 +10 89624266 COSM5101 A G . . GENE=PTEN;STRAND=+;CDS=c.40A>G;AA=p.R14G;CNT=1 +10 89624267 COSM284348 G T . . GENE=PTEN;STRAND=+;CDS=c.41G>T;AA=p.R14M;CNT=1 +10 89624269 COSM1159817 A G . . GENE=PTEN;STRAND=+;CDS=c.43A>G;AA=p.R15G;CNT=1 +10 89624270 COSM214443 GAT G . . GENE=PTEN;STRAND=+;CDS=c.45_46delAT;AA=p.Y16fs*27;CNT=1 +10 89624274 COSM346197 T C . . GENE=PTEN;STRAND=+;CDS=c.48T>C;AA=p.Y16Y;CNT=1 +10 89624274 COSM921056 T G . . GENE=PTEN;STRAND=+;CDS=c.48T>G;AA=p.Y16*;CNT=1 +10 89624275 COSM5153 C T . . GENE=PTEN;STRAND=+;CDS=c.49C>T;AA=p.Q17*;CNT=2 +10 89624305 COSM163810 T G . . GENE=PTEN;STRAND=+;CDS=c.79T>G;AA=p.Y27D;CNT=2 +10 89685281 COSM685105 C G . . GENE=PTEN;STRAND=+;CDS=c.176C>G;AA=p.S59*;CNT=1 +10 89685287 COSM5042 A G . . GENE=PTEN;STRAND=+;CDS=c.182A>G;AA=p.H61R;CNT=1 +10 89685303 COSM5191 G T . . GENE=PTEN;STRAND=+;CDS=c.198G>T;AA=p.K66N;CNT=1 +10 89685305 COSM921071 T C . . GENE=PTEN;STRAND=+;CDS=c.200T>C;AA=p.I67T;CNT=1 +10 89685307 COSM249839 T A . . GENE=PTEN;STRAND=+;CDS=c.202T>A;AA=p.Y68N;CNT=1 +10 89685314 COSM1162066 TG T . . GENE=PTEN;STRAND=+;CDS=c.209+1delg;AA=p.?;CNT=1 +10 89711873 COSM5963 A G . . GENE=PTEN;STRAND=+;CDS=c.493-2A>G;AA=p.?;CNT=1 +10 89711874 COSM5961 G A . . GENE=PTEN;STRAND=+;CDS=c.493-1G>A;AA=p.?;CNT=1 +10 89711874 COSM14213 GGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTATTATAGCTACCTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCA G . . GENE=PTEN;STRAND=+;CDS=c.493_634del142;AA=p.?;CNT=1 +10 89711875 COSM5091 G A . . GENE=PTEN;STRAND=+;CDS=c.493G>A;AA=p.G165R;CNT=3 +10 89711876 COSM5114 G A . . GENE=PTEN;STRAND=+;CDS=c.494G>A;AA=p.G165E;CNT=2 +10 89711877 COSM314554 A T . . GENE=PTEN;STRAND=+;CDS=c.495A>T;AA=p.G165G;CNT=1 +10 89711884 COSM1192818 AT A . . GENE=PTEN;STRAND=+;CDS=c.503delT;AA=p.S170fs*13;CNT=1 +10 89711891 COSM5045 G A . . GENE=PTEN;STRAND=+;CDS=c.509G>A;AA=p.S170N;CNT=2 +10 89711893 COSM685103 C A . . GENE=PTEN;STRAND=+;CDS=c.511C>A;AA=p.Q171K;CNT=1 +10 89711898 COSM297456 G A . . GENE=PTEN;STRAND=+;CDS=c.516G>A;AA=p.R172R;CNT=1 +10 89711899 COSM5089 C T . . GENE=PTEN;STRAND=+;CDS=c.517C>T;AA=p.R173C;CNT=1 +10 89711900 COSM5039 G A . . GENE=PTEN;STRAND=+;CDS=c.518G>A;AA=p.R173H;CNT=1 +10 89711905 COSM76106 G T . . GENE=PTEN;STRAND=+;CDS=c.523G>T;AA=p.V175L;CNT=1 +10 89711913 COSM13116 T A . . GENE=PTEN;STRAND=+;CDS=c.531T>A;AA=p.Y177*;CNT=1 +10 89711935 COSM216385 C G . . GENE=PTEN;STRAND=+;CDS=c.553C>G;AA=p.H185D;CNT=1 +10 89712017 COSM5968 G T . . GENE=PTEN;STRAND=+;CDS=c.634+1G>T;AA=p.?;CNT=1 +10 89712018 COSM428086 T C . . GENE=PTEN;STRAND=+;CDS=c.634+2T>C;AA=p.?;CNT=1 +10 89717607 COSM1167768 CAGATCCTCAGTTT C . . GENE=PTEN;STRAND=+;CDS=c.635-2_645delagATCCTCAGTTT;AA=p.?;CNT=1 +10 89717609 COSM28920 G A . . GENE=PTEN;STRAND=+;CDS=c.635-1G>A;AA=p.?;CNT=2 +10 89717609 COSM5971 G T . . GENE=PTEN;STRAND=+;CDS=c.635-1G>T;AA=p.?;CNT=1 +10 89717609 COSM921121 G C . . GENE=PTEN;STRAND=+;CDS=c.635-1G>C;AA=p.?;CNT=1 +10 89717609 COSM26624 GATCCTCAGTTTGTGGTCTGCCAGCTAAAGGTGAAGATATATTCCTCCAATTCAGGACCCACACGACGGGAAGACAAGTTCATGTACTTTGAGTTCCCTCAGCCGTTACCTGTGTGTGGTGATATCAAAGTAGAGTTCTTCCACAAACAGAACAAGATGCTAAAAAAGGTTTGTACTTTACTTTCATTGGGAGAAATATCCAAAATAAGGACAGATTAAAAGCTATATTTTATTTTATGACATGTAAGGAACTATAATTTGTTTTCTATTAGATCTGCAGGTGTTTTGCTTACTCTGGCATTGGTGAGACATTATAAGGGTAAATAATCCTGTTTGAAGGAAAAGGCCTTATGGCATTGTAACATGAGAGGAATTTTTCTTAACAAGGATGGTTAACTGAGAAGAAATTAGCATGGGACCAATATTTTAAAAATTTTGGTCTATAGGTAGAAATGAGATCTGTTCTGTGGTCTTATGTAGTGACACAAACCACTTTTTCTCCATTTTGGCTTATGTTTCTTTTTCTTTCCTTTTTTTTTTTTTTCCTTTTTGTTAGAGACAGGGTCTTGTTCTATTGCCCAGGCTGAGTAGCTAAGACTACAAGCATGTGCCACCACACCCAGCTAATTTTTTTTATTTTTATTTTTGTAGGGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCACAAGCAGTCCTCACGCTTTGGCATCCCAAAGAGTTGGAATTACAGGTGTGCGCCATCATGCCTGGCCTTAACGTTTCTTAAGACTTGATTATTTTCTATTTAGCTTCTGTGGATTTACTGATTAATTTTTTAACTAGGAGAGAAATCAGTATGAAGAGGAAGTAATAAAGAATGAAAACATGGTATTTAAATGTGCAGGTTTAGAAAGTTAATGAAGTTTGAATTTGATTGATCTGTATTTAGAGAAGGCAACGTCTTATTATTTTAAAACCAACTATCCGCCCTGTGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGTGGGCAGATCAGCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTTAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCGGGTGTGGTGGCAGGCGCCTGTTTTCCCAGCTACTCAGGAGGCTTGAGGCAGGATAATTGCTGAACCCGAGAGGCGGAGGTTGCAGTAAGCCAAGAATGCACCATTGTACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAAAAAAGAAAAAAAAAACAACAACTATCTTCATTTAAAATATTAAATGTGAATATTTAAAGTGAGACTAAGGTGCAACATTTTTAGATAGTAATGAAGAAAAGGACTAACTTTGTAGTGTTGCTGCCTTGTTAAACATACTAGATAGCATATTGCCAATCTTTAAACATTCTCAATGATAGGATTTATTTACTTTTTCTGATTTTTAGCTTTTCTTTTGAAAGAAAATAAGAGGAAGTTTCATTTACTGCAAAATTTTAAATGCTGCTTTGATGTATCAGTAGAGATATAATTTTCCTTTATCCAGAATCCAAGTAGCTGGAAAAAAAAATCAAAATATGCTGAACTTTTTTTTTTTTAGCCAGAAACCCATTTCCTATCGTCTGTACAAATAAAAGTTAAATATATCTCAATAACTTAGAAAAATTATTTTTTGATAATCCAGGAAGTATTAGCAACTGTTTTAAAATTAAGATAACTAGTAAGTTTTATTTAGCTTTCAAAAATAGGCATCTACATCATCATCTCTGCATACCTTTAGGAATTTCCTAATTCTTATTTCCCTTCATCTGTACTTTAACACATGCAAAATTGAAGGTTAGATTAAATATTTATGATTTATTTGTTTATCCTTGACTACATAAATTTCCATTTTATTGATTTTCCCTGCCTTATTTAAGAATATGCTATGATTAAAACACAAAAAATTTTAGTATAACCCATATATATATAGAATTCACCTTTTTGTTATTTAAATATTATTGGCTTATTTTCTTCTAAGTAAAATACAATTACTGGCTAAAATAATTGAAATAAGCAAAAAAAAAATTTTAAAGACCTTGTATACAAGATTACTTTGCCAGGTACTGTTAAAAGATGCAATGACATTTAAGACGTAACATCCTTAAGGATCTTATTTTCTGGGGGATAAAAAACTTTAAGATAAATTAGAATAAAAGATTTAAATGGCATTTTAAGGTACCAGGTACCAGATAAGATGTCACAAGGCTGTATATCATTAATTGCCAAATGATTTATACAGGCCAGATTTCTTTGTTGGTCAATAGAGGTTTAAAGTGATGAACTTCTGTTGTGTTTTTTTATTAAGAAGGTATTATCTTATTAGTAAGAAGTGATTTTTTTTAAGAACAAGCATTTTATAACATCAAAAGAAATCAGTAGTACTCTTTCCTACCCCCTCATATTTATTCTGAAAGTATTCAAGCATTATATTGTCATGTAAGAAACTGGAGCTTCTCATGTTTGTATTGCTGTAGAAGTAAACATGTATTTGCCATGCGTCATCAGGGAAGTTGCACTCACCGTCCAAGAACTTTTGTTAAAGTAAATCTTGGAATAGGTAGCTCATTTGAAATGTAGAAAAAATTAAATCCATATCTGAATTTTGTTTATATGTATGTACACGTAAACTAAAAACGTATTTAAAGCTAGTATTAGATGAGAAAAGAGGTTTTTTTACTTAAAATTTTAAGGCAAAAGTAGTTTATCTTAGATCTTGTGAGATTGTATTTTTGGTTTAAAATTTGAGAATTTGAGTGAAGAAAAATCATGTGAATGAAAATGCAACAGATAACTCAGATTGCCTTATAATAGTCTTTGTGTTTACCTTTATTCAGAATATCAAATGATAGTTTATTTTGTTGACTTTTTGCAAATGTTTAACATAGGTGACAGATTTTCTTTTTTAAAAAAATAAAACATCATTAATTAAATATGTCATTTCATTTCTTTTTCTTTTCTTTTTTTTTTTTTTTAGGACAAAATGTTTCACTTTTGGGTAAATACATTCTTCATACCAGGACCAGAGGAAACCTCAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATCGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACAAAGCCAACCGATACTTTTCTCCAAATTTTAAGGTCAGTTAAATTAAACATTTTGTGGGGGTTGTTGACTTGTATGTATGTGATGTGTGTTTAATTCTAGGAGTACAGCTGATGAAGAACTTGCTTGACAAGTTTTTAACTTATGTATTATTTCGAAGCAGTGTTTACGTAGCAGTAACATGAAAGTTTCTAATAAAATACCCAATGTACACAGCGTCAAAAAAGCTGCATTTTTCCTTTTCCTAATTCTTCGTTGTTTGCTGAAATCTGGGGCAAAGGTGCGGGAGGGGGCTAAATGACTGGGATATGAAGTAGGAATGGGAGAGGAAAGAAATAGATGGGAACTCAGTCATTTGGGAATGATTCATATGGAATGTTTTTACTGCTTCCACTCCTGTCTGCCTTCCAATTTATTCTCAATCCCTCAGAGTGATCTTAAAAATAGACTTGATTGTGTCACTTCTGTTTACACTTTATAAGGACCTTGTGTTTTTTTTTTTACCATGACCTACAAGGCCCAGCATAATTTAGCACAGGGCTACCTCCTACATCAGCACTAGTCACCTTCTCTCCTTGTTTCTTGAGATTCAGTCATACTGGTCTTTCTTCAGTTCTTCAAAATGCTAAGCTTCTGCCTCTTCTAGTCTTTCCAGTTATTTTCCTTCTCCCTGTACCTTTTCATCTCAGCCTTTTCCCCTGACCTTCCATAGCTATCTTCATATTTCCAGCCTTAGCTTCAATCTCATATTCTCTGAAGTCCTTTGATTGTCCTCCCGTTATTCTTTTTTTAAAAATCCTATTTCCTTATATTGTATCTTAGAATTATTTGGTTTGTTTCATTTTTGCCTATGTGTGATATATGTATTTCTACATAGGTATATATATCTACTTATAGACAAGAATTCTTCAGATTAAAAAAATCTGATTTGTAAACATTCCCAAGTGGTTGTTTACCATTTTTTTCTTCCCCCTTCCTATTTCTTATTCTACCTGATTTTCCCCTGTTCATTCACCACACTCGTTTCTTTCTCTTTTTTACTCTCTCTTAATTTTTCATTCAATTTTTATAACATGTAATAAATCTAACTGTAGCGTCTGAGTATTAAGAATATTGCTAGTAATACTTCACCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGCGGATCACTTGAGGCCCAGGAGTTTAAGACCAGCCGGCCAATATGGCGAAACCCTATCTGCACTACAAATACAAAAATTAGCTGGGCATGGTGTCGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACAAGAATTGCTTGAGCCTGTGAGATGGAGGTTGCAGTGAGCCGAGATCACACCAGTGCACGTGCACTTCAGCCTGGGCAACAGAGCAAGACTCTGTCTTAAAAAAAAAAAAAAAAAAAAAATATATACACACACACACACACACACACACACACACACACACTATTACTACCAATATACATACATATATGTATGTATGTATGTATGTATATTGGTAGTAATAGTAATACTTGGGCCCCTGCACGTTTTAAGTGAAAATAGATCTAATATTAAATGTCTTTAGCCCTTAAATTTTTTTTAAGTGTTCAGAAGTTTCCCTTTAAAAAAATTTTTAATATATAATAATTGTACATATTTATGGGATACAGAGTGATATTTTCATGTATGCAGTGTGTGATGATCAAATCAGGATAATTAGCATATGGATCACCTCAAACATTTGTCATTTCTTTGTGTTAGGAACATTCAAAATTCTGTCTTCTAGCTATTTGAAAATATACAGTAAATTATTGTTGACTAGTTACAGTTCTATAGAACACTATAATTTATTCCTCCTGTGTGTAATTTTTTATCTTTTAACCAACATCTCCCTATCCTCCCCTCCCACTCCCTTTCCCGGCCTCTAATAACCACACTCTTATGAGCTCAACTTTTTTAGCTTCCATATATGAGTGAGAACATACGGTATTTATCTTTCTGTACCTGACTTATTTTACTTAACATCATGTCCTCCGGGCTAGACATTCTCTTTAGAATCCACAGGTTTCCTTTCTTTTCTCTAAATCTGCATTTTGCTCAGCCATTAACTTTTAAAATGTCTTTTTCCCTTTAGTTTTATTGTTTTCTATTTTAATATTGCAAGATGTTTTATATTTGTGATTACAAATAAAAACTCCATTATTAGTAAACAAATACAATGTCATATAGTAGTAAGTGCTATAAAAAATAGACAGGATAGAAAGTAATCTTGGTTTGTATGTTTTTTGTTTTTTAGCAAAGATGATTAGAGAAGGCCCAACCAAGCAGATAACATTTAAGCAGAGGCCTAAATCATATAAGTGAGTTATACAAATATCTGGGAAAAGAGTTAAGAGTACAGATGCAAAAGCCCTTAGACAAGAGAATGAGCTTGGTATATCTGAAGAGTGGATAAGTCATTTTGACTGAAACAGAGTGGACAAGAAAACCAGTCCAAGTGTAAAGACACTAGTGTGTGTTCAGCATAGGAAGGATGTAATCTGAATTTTGTGTTTAATATTCCCTGTGTTCATGCTTTCAAAATACAGATGAGTGAGGAAAGTAGGGAGAAGGGGTAATAAAGGAAGCTGAGAGATCAGTTAAGAGGTACTTGAATAGTTTAGTAAAGATGAGAGAAGATGTTTGCTTCTTGTTGCCCCTCACTGCTTAGAATAGTGGCAGTGAAGGGTAACAAGAAGCTGTCAGATTAACTTAAAGAGTTTACTGATGCAGTGGATGTTGGTTGTAAGAGAAGAATTGATAATGACTCTTGGATAATAGGGGAGGGAGGGGCTGTCAATATAATATAATGAAGAAGGGATTTGAAGTCATTTCTGATTTAAATCTCACATCCACTACCTACTTTTAATAGATATGTAGCCTTTAACAAGTTCCCTAACCTTTCTGGGCCTTAGCTACCTCCCCTTGGAAATGGAAATACCTAACATGTAAGGTTGTTTTGACAGTTATTTTCACTAGGCATGTAAAGGCACTTGACTCTCTGTTATAGACCACTGTATTATGTTAATGTCCCTCTCCTTCCTCCCTTTAGGTAAAGTTTTTAGGGCTAATAAATCCCAAATATCAATGTTGATCAGTAGTTTGTGTTTGTGTAGTGTTGTTTATATCAAAAACTACATTGAAGCCGGGCACAGTGGTTCACGCCTAAAATCGCAACACTTTGGGAGGCCAAGGTGGGCCTCCCACCTTGAACTAAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAATCCCATCTCTACAAAAAATATAAAAGCTAGCTGGGTGTGGTGGCATGCACCTGTAGTCCTAGCTACTTGGGAGGCTGAGGTTGATCCTGGGAGTTTGAGCCTGCAGTGAGCTGTGAAGATGCCACTGCACTCTAGTCTGGGTGACAGAGCAAGACCCTGTCTCAAAAACACACACACACACACACACACACACAAAGAAATACATTGATTTTTCACATAGGTAGTAAGAGAAACATTCTTTTTGAACTCAGCTGTTTGTGAATTGAATTTTGTAATTCAAATGCTATATTATGTAAACTATTGATGACTTTCAATCTGCATTTATTTTGTATAATTATTTAGTTAATATTTGCCACTTATATTCCTTAAAAAATAAAATTGAGGTTGGGCGTGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATTGCCTGAGCTCAGGAGTTTGAGATCAGCCTGGGCAACATCATGAACCCCATTTCTACTAAAATACAAAAAATTATCTGGGCATGGTGGTGTACACCTGTAGCCCTAGCTGTTTGGGAGGCTAAGGCACGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCTTGGCAACAGAGCAAGACTCTTGTCTCCAGAAATAAAAATAAATAAATTGTATTAACATCCTGATAGTTTATCTGTTTAGTACCTAGCAAGAAAGAAAATGTTGAACATCTTAAGAAGAGGGTCATTTAAAAGGCCTCTTAAAGATCATGTTTGTTACAGTGCTTAAAAATTAATATGTTCATCTGCAAAATGGAATAAAAAATCTGTTAAAAATATATTTCACTAAATAGTTTAAGATGAGTCATATTTGTGGGTTTTCATTTTAAATTTTCTTTCTCTAGGTGAAGCTGTACTTCACAAAAACAGTAGAGGAGCCGTCAAATCCAGAGGCTAGCAGTTCAACTTCTGTAACACCAGATGTTAGTGACAATGAACCTGATCATTATAGATATTCTGACACCACTGACTCTGATCCAGAGAATGAACCTTTTGATGAAGATCAGCATACACAAATTACAAAAGTCTGA G . . GENE=PTEN;STRAND=+;CDS=c.635_1212del578;AA=p.N212fs*1;CNT=1 +10 89717613 COSM241294 C G . . GENE=PTEN;STRAND=+;CDS=c.638C>G;AA=p.P213R;CNT=1 +10 89717615 COSM5150 C T . . GENE=PTEN;STRAND=+;CDS=c.640C>T;AA=p.Q214*;CNT=2 +10 89717619 COSM212632 T C . . GENE=PTEN;STRAND=+;CDS=c.644T>C;AA=p.F215S;CNT=1 +10 89717625 COSM1159818 T A . . GENE=PTEN;STRAND=+;CDS=c.650T>A;AA=p.V217D;CNT=1 +10 89717671 COSM69004 AC A . . GENE=PTEN;STRAND=+;CDS=c.697delC;AA=p.R233fs*23;CNT=1 +10 89717672 COSM5154 C T . . GENE=PTEN;STRAND=+;CDS=c.697C>T;AA=p.R233*;CNT=14 +10 89717676 COSM540238 G T . . GENE=PTEN;STRAND=+;CDS=c.701G>T;AA=p.R234L;CNT=2 +10 89717678 COSM5292 G T . . GENE=PTEN;STRAND=+;CDS=c.703G>T;AA=p.E235*;CNT=1 +10 89717695 COSM921125 C G . . GENE=PTEN;STRAND=+;CDS=c.720C>G;AA=p.Y240*;CNT=1 +10 89717697 COSM5126 T C . . GENE=PTEN;STRAND=+;CDS=c.722T>C;AA=p.F241S;CNT=1 +10 89717708 COSM5159 C T . . GENE=PTEN;STRAND=+;CDS=c.733C>T;AA=p.Q245*;CNT=2 +10 89717712 COSM5111 C T . . GENE=PTEN;STRAND=+;CDS=c.737C>T;AA=p.P246L;CNT=1 +10 89717712 COSM1167796 C CGTAA . . GENE=PTEN;STRAND=+;CDS=c.737_738insGTAA;AA=p.L247fs*1;CNT=1 +10 89717712 COSM5822 CG C . . GENE=PTEN;STRAND=+;CDS=c.738delG;AA=p.P246fs*10;CNT=1 +10 89717716 COSM685102 A C . . GENE=PTEN;STRAND=+;CDS=c.741A>C;AA=p.L247F;CNT=1 +10 89717718 COSM685101 C A . . GENE=PTEN;STRAND=+;CDS=c.743C>A;AA=p.P248H;CNT=1 +10 89717718 COSM166165 CTG C . . GENE=PTEN;STRAND=+;CDS=c.744_745delTG;AA=p.C250fs*2;CNT=1 +10 89717721 COSM921128 T A . . GENE=PTEN;STRAND=+;CDS=c.746T>A;AA=p.V249E;CNT=1 +10 89717727 COSM13981 G A . . GENE=PTEN;STRAND=+;CDS=c.752G>A;AA=p.G251D;CNT=2 +10 89717729 COSM5246 G T . . GENE=PTEN;STRAND=+;CDS=c.754G>T;AA=p.D252Y;CNT=2 +10 89717739 COSM921130 T G . . GENE=PTEN;STRAND=+;CDS=c.764T>G;AA=p.V255G;CNT=1 +10 89717762 COSM43075 A T . . GENE=PTEN;STRAND=+;CDS=c.787A>T;AA=p.K263*;CNT=1 +10 89717778 COSM921136 T C . . GENE=PTEN;STRAND=+;CDS=c.801+2T>C;AA=p.?;CNT=1 +10 89720726 COSM5303 G T . . GENE=PTEN;STRAND=+;CDS=c.877G>T;AA=p.G293*;CNT=1 +10 89720741 COSM5156 C T . . GENE=PTEN;STRAND=+;CDS=c.892C>T;AA=p.Q298*;CNT=3 +10 89720744 COSM5312 G T . . GENE=PTEN;STRAND=+;CDS=c.895G>T;AA=p.E299*;CNT=1 +10 89720798 COSM39615 GTACT G . . GENE=PTEN;STRAND=+;CDS=c.950_953delTACT;AA=p.L318fs*2;CNT=3 +10 89720808 COSM35671 T A . . GENE=PTEN;STRAND=+;CDS=c.959T>A;AA=p.L320*;CNT=1 +10 89720817 COSM4990 A AA . . GENE=PTEN;STRAND=+;CDS=c.968_969insA;AA=p.N323fs*2;CNT=1 +10 89720823 COSM921154 T G . . GENE=PTEN;STRAND=+;CDS=c.974T>G;AA=p.L325R;CNT=1 +10 89720826 COSM5128 A G . . GENE=PTEN;STRAND=+;CDS=c.977A>G;AA=p.D326G;CNT=1 +10 89720852 COSM921156 C G . . GENE=PTEN;STRAND=+;CDS=c.1003C>G;AA=p.R335G;CNT=1 +10 89720852 COSM5151 C T . . GENE=PTEN;STRAND=+;CDS=c.1003C>T;AA=p.R335*;CNT=3 +10 89720857 COSM5290 C G . . GENE=PTEN;STRAND=+;CDS=c.1008C>G;AA=p.Y336*;CNT=2 +10 89720875 COSM921159 G T . . GENE=PTEN;STRAND=+;CDS=c.1026G>T;AA=p.K342N;CNT=1 +10 89720876 COSM5978 G A . . GENE=PTEN;STRAND=+;CDS=c.1026+1G>A;AA=p.?;CNT=1 +10 123258030 COSM174658 G T . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.1384C>A;AA=p.L462I;CNT=1 +10 123258030 COSM174657 G T . . GENE=FGFR2;STRAND=-;CDS=c.1651C>A;AA=p.L551I;CNT=1 +10 123258034 COSM427158 A T . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.1380T>A;AA=p.N460K;CNT=4 +10 123258034 COSM427159 A T . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.1641T>A;AA=p.N547K;CNT=4 +10 123258034 COSM1152148 A T . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.1650T>A;AA=p.N550K;CNT=4 +10 123258034 COSM36912 A T . . GENE=FGFR2;STRAND=-;CDS=c.1647T>A;AA=p.N549K;CNT=4 +10 123258070 COSM915489 C A . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.1605G>T;AA=p.M535I;CNT=1 +10 123258070 COSM915487 C A . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.1344G>T;AA=p.M448I;CNT=1 +10 123258070 COSM915488 C A . . GENE=FGFR2;STRAND=-;CDS=c.1611G>T;AA=p.M537I;CNT=1 +10 123258070 COSM1152149 C A . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.1614G>T;AA=p.M538I;CNT=1 +10 123258086 COSM227560 A C . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.1328T>G;AA=p.V443G;CNT=1 +10 123258086 COSM227559 A C . . GENE=FGFR2;STRAND=-;CDS=c.1595T>G;AA=p.V532G;CNT=1 +10 123274774 COSM36906 A G . . GENE=FGFR2;STRAND=-;CDS=c.1144T>C;AA=p.C382R;CNT=1 +10 123274774 COSM915497 A G . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.1144T>C;AA=p.C382R;CNT=1 +10 123274774 COSM915496 A G . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.877T>C;AA=p.C293R;CNT=1 +10 123274774 COSM1152150 A G . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.1147T>C;AA=p.C383R;CNT=1 +10 123274794 COSM915499 T C . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.1124A>G;AA=p.Y375C;CNT=1 +10 123274794 COSM915498 T C . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.857A>G;AA=p.Y286C;CNT=1 +10 123274794 COSM1152151 T C . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.1127A>G;AA=p.Y376C;CNT=1 +10 123274794 COSM36904 T C . . GENE=FGFR2;STRAND=-;CDS=c.1124A>G;AA=p.Y375C;CNT=1 +10 123279562 COSM41286 C G . . GENE=FGFR2;STRAND=-;CDS=c.870G>C;AA=p.W290C;CNT=1 +10 123279562 COSM1146411 C G . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.870G>C;AA=p.W290C;CNT=1 +10 123279562 COSM683046 C G . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.870G>C;AA=p.W290C;CNT=1 +10 123279562 COSM683045 C G . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.603G>C;AA=p.W201C;CNT=1 +10 123279674 COSM537801 G A . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.491C>T;AA=p.P164L;CNT=1 +10 123279674 COSM537803 G A . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.758C>T;AA=p.P253L;CNT=1 +10 123279674 COSM915504 G C . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.491C>G;AA=p.P164R;CNT=1 +10 123279674 COSM1139349 G A . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.758C>T;AA=p.P253L;CNT=1 +10 123279674 COSM1152152 G C . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.758C>G;AA=p.P253R;CNT=1 +10 123279674 COSM915505 G C . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.758C>G;AA=p.P253R;CNT=1 +10 123279674 COSM49170 G C . . GENE=FGFR2;STRAND=-;CDS=c.758C>G;AA=p.P253R;CNT=1 +10 123279674 COSM537802 G A . . GENE=FGFR2;STRAND=-;CDS=c.758C>T;AA=p.P253L;CNT=1 +10 123279677 COSM915507 G C . . GENE=FGFR2_ENST00000351936;STRAND=-;CDS=c.755C>G;AA=p.S252W;CNT=13 +10 123279677 COSM915506 G C . . GENE=FGFR2_ENST00000357555;STRAND=-;CDS=c.488C>G;AA=p.S163W;CNT=13 +10 123279677 COSM36903 G C . . GENE=FGFR2;STRAND=-;CDS=c.755C>G;AA=p.S252W;CNT=13 +10 123279677 COSM1152153 G C . . GENE=FGFR2_ENST00000457416;STRAND=-;CDS=c.755C>G;AA=p.S252W;CNT=13 +11 533860 COSM161605 C T . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.196G>A;AA=p.A66T;CNT=1 +11 533860 COSM161604 C T . . GENE=HRAS;STRAND=-;CDS=c.196G>A;AA=p.A66T;CNT=1 +11 533874 COSM498 T A . . GENE=HRAS;STRAND=-;CDS=c.182A>T;AA=p.Q61L;CNT=3 +11 533874 COSM499 T C . . GENE=HRAS;STRAND=-;CDS=c.182A>G;AA=p.Q61R;CNT=2 +11 533874 COSM99664 T A . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.182A>T;AA=p.Q61L;CNT=3 +11 533874 COSM244958 T C . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.182A>G;AA=p.Q61R;CNT=2 +11 533875 COSM123649 G T . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.181C>A;AA=p.Q61K;CNT=3 +11 533875 COSM496 G T . . GENE=HRAS;STRAND=-;CDS=c.181C>A;AA=p.Q61K;CNT=3 +11 534282 COSM238587 A C . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.41T>G;AA=p.V14G;CNT=1 +11 534282 COSM238586 A C . . GENE=HRAS;STRAND=-;CDS=c.41T>G;AA=p.V14G;CNT=1 +11 534285 COSM120918 C A . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.38G>T;AA=p.G13V;CNT=2 +11 534285 COSM489 C A . . GENE=HRAS;STRAND=-;CDS=c.38G>T;AA=p.G13V;CNT=2 +11 534286 COSM488 C A . . GENE=HRAS;STRAND=-;CDS=c.37G>T;AA=p.G13C;CNT=1 +11 534286 COSM99938 C G . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.37G>C;AA=p.G13R;CNT=3 +11 534286 COSM486 C G . . GENE=HRAS;STRAND=-;CDS=c.37G>C;AA=p.G13R;CNT=3 +11 534286 COSM689078 C A . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.37G>T;AA=p.G13C;CNT=1 +11 534288 COSM484 C T . . GENE=HRAS;STRAND=-;CDS=c.35G>A;AA=p.G12D;CNT=3 +11 534288 COSM120919 C G . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.35G>C;AA=p.G12A;CNT=1 +11 534288 COSM485 C G . . GENE=HRAS;STRAND=-;CDS=c.35G>C;AA=p.G12A;CNT=1 +11 534288 COSM99915 C T . . GENE=HRAS_ENST00000397594;STRAND=-;CDS=c.35G>A;AA=p.G12D;CNT=3 +11 108117844 COSM1183957 T A . . GENE=ATM;STRAND=+;CDS=c.1055T>A;AA=p.I352N;CNT=2 +11 108117844 COSM1183956 T A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.1055T>A;AA=p.I352N;CNT=2 +11 108119810 COSM1146564 G A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.1216G>A;AA=p.D406N;CNT=1 +11 108119810 COSM685593 G A . . GENE=ATM;STRAND=+;CDS=c.1216G>A;AA=p.D406N;CNT=1 +11 108119829 COSM352332 G T . . GENE=ATM;STRAND=+;CDS=c.1235G>T;AA=p.W412L;CNT=1 +11 108123582 COSM200656 G A . . GENE=ATM;STRAND=+;CDS=c.1841G>A;AA=p.S614N;CNT=1 +11 108123623 COSM1139582 C T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.1882C>T;AA=p.Q628*;CNT=1 +11 108123623 COSM540414 C T . . GENE=ATM;STRAND=+;CDS=c.1882C>T;AA=p.Q628*;CNT=1 +11 108123641 COSM1158827 T A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.1898+2T>A;AA=p.?;CNT=2 +11 108123641 COSM1158828 T A . . GENE=ATM;STRAND=+;CDS=c.1898+2T>A;AA=p.?;CNT=2 +11 108137952 COSM1139584 G T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.2521G>T;AA=p.D841Y;CNT=1 +11 108137952 COSM540412 G T . . GENE=ATM;STRAND=+;CDS=c.2521G>T;AA=p.D841Y;CNT=1 +11 108138007 COSM365639 A T . . GENE=ATM;STRAND=+;CDS=c.2576A>T;AA=p.N859I;CNT=1 +11 108155174 COSM685592 A G . . GENE=ATM;STRAND=+;CDS=c.3967A>G;AA=p.K1323E;CNT=1 +11 108155174 COSM1146565 A G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.3967A>G;AA=p.K1323E;CNT=1 +11 108155202 COSM1183954 T C . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.3993+2T>C;AA=p.?;CNT=2 +11 108155202 COSM1183955 T C . . GENE=ATM;STRAND=+;CDS=c.3993+2T>C;AA=p.?;CNT=2 +11 108170450 COSM371274 G T . . GENE=ATM;STRAND=+;CDS=c.5015G>T;AA=p.G1672V;CNT=1 +11 108170450 COSM1127934 G C . . GENE=ATM;STRAND=+;CDS=c.5015G>C;AA=p.G1672A;CNT=1 +11 108170460 COSM1146568 G T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5025G>T;AA=p.L1675F;CNT=1 +11 108170460 COSM685589 G T . . GENE=ATM;STRAND=+;CDS=c.5025G>T;AA=p.L1675F;CNT=1 +11 108170468 COSM466266 T G . . GENE=ATM;STRAND=+;CDS=c.5033T>G;AA=p.V1678G;CNT=1 +11 108170468 COSM1135095 T G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5033T>G;AA=p.V1678G;CNT=1 +11 108170469 COSM540834 G T . . GENE=ATM;STRAND=+;CDS=c.5034G>T;AA=p.V1678V;CNT=1 +11 108170469 COSM1139590 G T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5034G>T;AA=p.V1678V;CNT=1 +11 108170587 COSM218294 C G . . GENE=ATM;STRAND=+;CDS=c.5152C>G;AA=p.L1718V;CNT=2 +11 108170587 COSM1159126 C G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5152C>G;AA=p.L1718V;CNT=1 +11 108173640 COSM12792 C T . . GENE=ATM;STRAND=+;CDS=c.5380C>T;AA=p.L1794L;CNT=2 +11 108173681 COSM159255 G A . . GENE=ATM;STRAND=+;CDS=c.5421G>A;AA=p.K1807K;CNT=1 +11 108173724 COSM272064 G T . . GENE=ATM;STRAND=+;CDS=c.5464G>T;AA=p.E1822*;CNT=1 +11 108173736 COSM1183962 T G . . GENE=ATM;STRAND=+;CDS=c.5476T>G;AA=p.L1826V;CNT=2 +11 108173736 COSM1183961 T G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5476T>G;AA=p.L1826V;CNT=2 +11 108180931 COSM1127930 T C . . GENE=ATM;STRAND=+;CDS=c.5807T>C;AA=p.L1936S;CNT=1 +11 108181051 COSM685587 A C . . GENE=ATM;STRAND=+;CDS=c.5918+9A>C;AA=p.?;CNT=1 +11 108181051 COSM1146570 A C . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.5918+9A>C;AA=p.?;CNT=1 +11 108200958 COSM12951 A C . . GENE=ATM;STRAND=+;CDS=c.7325A>C;AA=p.Q2442P;CNT=1 +11 108200961 COSM20404 G A . . GENE=ATM;STRAND=+;CDS=c.7328G>A;AA=p.R2443Q;CNT=1 +11 108200998 COSM428363 G A . . GENE=ATM;STRAND=+;CDS=c.7365G>A;AA=p.L2455L;CNT=1 +11 108200998 COSM1133925 G A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.7365G>A;AA=p.L2455L;CNT=1 +11 108201009 COSM332194 G C . . GENE=ATM;STRAND=+;CDS=c.7376G>C;AA=p.R2459P;CNT=1 +11 108204678 COSM540830 C A . . GENE=ATM;STRAND=+;CDS=c.7993C>A;AA=p.P2665T;CNT=1 +11 108204678 COSM1139594 C A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.7993C>A;AA=p.P2665T;CNT=1 +11 108205756 COSM922745 C T . . GENE=ATM;STRAND=+;CDS=c.8071C>T;AA=p.R2691C;CNT=1 +11 108205756 COSM1176661 C T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8071C>T;AA=p.R2691C;CNT=1 +11 108205763 COSM265665 CAGG C . . GENE=ATM;STRAND=+;CDS=c.8079_8081delAGG;AA=p.G2695delG;CNT=1 +11 108205768 COSM540828 G T . . GENE=ATM;STRAND=+;CDS=c.8083G>T;AA=p.G2695C;CNT=1 +11 108205768 COSM1139596 G T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8083G>T;AA=p.G2695C;CNT=1 +11 108205768 COSM1139595 G A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8083G>A;AA=p.G2695S;CNT=1 +11 108205768 COSM540829 G A . . GENE=ATM;STRAND=+;CDS=c.8083G>A;AA=p.G2695S;CNT=2 +11 108206572 COSM466271 G C . . GENE=ATM;STRAND=+;CDS=c.8152G>C;AA=p.G2718R;CNT=1 +11 108206572 COSM1135100 G C . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8152G>C;AA=p.G2718R;CNT=1 +11 108206578 COSM540827 G C . . GENE=ATM;STRAND=+;CDS=c.8158G>C;AA=p.D2720H;CNT=1 +11 108206578 COSM1139597 G C . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8158G>C;AA=p.D2720H;CNT=1 +11 108206578 COSM1133926 G A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8158G>A;AA=p.D2720N;CNT=1 +11 108206578 COSM428364 G A . . GENE=ATM;STRAND=+;CDS=c.8158G>A;AA=p.D2720N;CNT=1 +11 108206581 COSM200673 G A . . GENE=ATM;STRAND=+;CDS=c.8161G>A;AA=p.D2721N;CNT=1 +11 108218083 COSM415350 A T . . GENE=ATM;STRAND=+;CDS=c.8662A>T;AA=p.I2888L;CNT=1 +11 108218083 COSM1133334 A T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8662A>T;AA=p.I2888L;CNT=1 +11 108218084 COSM21679 T C . . GENE=ATM;STRAND=+;CDS=c.8663T>C;AA=p.I2888T;CNT=1 +11 108218090 COSM1139599 T G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.8669T>G;AA=p.L2890R;CNT=1 +11 108218090 COSM540823 T G . . GENE=ATM;STRAND=+;CDS=c.8669T>G;AA=p.L2890R;CNT=1 +11 108218092 COSM168512 G C . . GENE=ATM;STRAND=+;CDS=c.8671G>C;AA=p.G2891R;CNT=1 +11 108236071 COSM922759 A G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9007A>G;AA=p.N3003D;CNT=1 +11 108236074 COSM466274 A G . . GENE=ATM;STRAND=+;CDS=c.9010A>G;AA=p.K3004E;CNT=1 +11 108236074 COSM1135102 A G . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9010A>G;AA=p.K3004E;CNT=1 +11 108236087 COSM21626 G A . . GENE=ATM;STRAND=+;CDS=c.9023G>A;AA=p.R3008H;CNT=2 +11 108236087 COSM356707 G T . . GENE=ATM;STRAND=+;CDS=c.9023G>T;AA=p.R3008L;CNT=1 +11 108236087 COSM1139600 G A . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9023G>A;AA=p.R3008H;CNT=2 +11 108236107 COSM1139601 G T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9043G>T;AA=p.E3015*;CNT=1 +11 108236107 COSM540821 G T . . GENE=ATM;STRAND=+;CDS=c.9043G>T;AA=p.E3015*;CNT=1 +11 108236172 COSM1162928 A T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9108A>T;AA=p.I3036I;CNT=1 +11 108236172 COSM1162929 A T . . GENE=ATM;STRAND=+;CDS=c.9108A>T;AA=p.I3036I;CNT=1 +11 108236203 COSM1152251 C T . . GENE=ATM_ENST00000278616;STRAND=+;CDS=c.9139C>T;AA=p.R3047*;CNT=1 +11 108236203 COSM21624 C T . . GENE=ATM;STRAND=+;CDS=c.9139C>T;AA=p.R3047*;CNT=1 +12 25378557 COSM124019 C G . . GENE=KRAS;STRAND=-;CDS=c.441G>C;AA=p.K147N;CNT=1 +12 25378561 COSM19900 G A . . GENE=KRAS;STRAND=-;CDS=c.437C>T;AA=p.A146V;CNT=1 +12 25378562 COSM19404 C T . . GENE=KRAS;STRAND=-;CDS=c.436G>A;AA=p.A146T;CNT=11 +12 25378562 COSM1165198 C T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.436G>A;AA=p.A146T;CNT=2 +12 25378562 COSM1140130 C G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.436G>C;AA=p.A146P;CNT=1 +12 25378562 COSM19905 C G . . GENE=KRAS;STRAND=-;CDS=c.436G>C;AA=p.A146P;CNT=2 +12 25378645 COSM692703 C G . . GENE=KRAS;STRAND=-;CDS=c.353G>C;AA=p.C118S;CNT=1 +12 25378645 COSM1146991 C G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.353G>C;AA=p.C118S;CNT=1 +12 25378647 COSM19940 T G . . GENE=KRAS;STRAND=-;CDS=c.351A>C;AA=p.K117N;CNT=2 +12 25378706 COSM288668 C A . . GENE=KRAS;STRAND=-;CDS=c.292G>T;AA=p.E98*;CNT=1 +12 25380254 COSM183929 C A . . GENE=KRAS;STRAND=-;CDS=c.204G>T;AA=p.R68S;CNT=1 +12 25380259 COSM329471 T G . . GENE=KRAS;STRAND=-;CDS=c.199A>C;AA=p.M67L;CNT=1 +12 25380268 COSM1212767 A G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.190T>C;AA=p.Y64H;CNT=1 +12 25380268 COSM1212768 A G . . GENE=KRAS;STRAND=-;CDS=c.190T>C;AA=p.Y64H;CNT=1 +12 25380275 COSM554 T G . . GENE=KRAS;STRAND=-;CDS=c.183A>C;AA=p.Q61H;CNT=9 +12 25380275 COSM1135364 T G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.183A>C;AA=p.Q61H;CNT=5 +12 25380275 COSM1146992 T A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.183A>T;AA=p.Q61H;CNT=4 +12 25380275 COSM555 T A . . GENE=KRAS;STRAND=-;CDS=c.183A>T;AA=p.Q61H;CNT=4 +12 25380276 COSM553 T A . . GENE=KRAS;STRAND=-;CDS=c.182A>T;AA=p.Q61L;CNT=6 +12 25380276 COSM1140131 T A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.182A>T;AA=p.Q61L;CNT=3 +12 25380276 COSM552 T C . . GENE=KRAS;STRAND=-;CDS=c.182A>G;AA=p.Q61R;CNT=5 +12 25380276 COSM1158660 T C . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.182A>G;AA=p.Q61R;CNT=2 +12 25380276 COSM87298 TGA TTT . . GENE=KRAS;STRAND=-;CDS=c.180_181TC>AA;AA=p.Q61K;CNT=2 +12 25380277 COSM549 G T . . GENE=KRAS;STRAND=-;CDS=c.181C>A;AA=p.Q61K;CNT=3 +12 25380277 COSM1159597 G T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.181C>A;AA=p.Q61K;CNT=2 +12 25380278 COSM1159613 A T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.180T>A;AA=p.G60G;CNT=2 +12 25380278 COSM253757 A T . . GENE=KRAS;STRAND=-;CDS=c.180T>A;AA=p.G60G;CNT=3 +12 25380279 COSM87290 C T . . GENE=KRAS;STRAND=-;CDS=c.179G>A;AA=p.G60D;CNT=1 +12 25380281 COSM1162236 T A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.177A>T;AA=p.A59A;CNT=1 +12 25380281 COSM1162237 T A . . GENE=KRAS;STRAND=-;CDS=c.177A>T;AA=p.A59A;CNT=1 +12 25380282 COSM28518 G C . . GENE=KRAS;STRAND=-;CDS=c.176C>G;AA=p.A59G;CNT=1 +12 25380282 COSM1135365 G C . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.176C>G;AA=p.A59G;CNT=1 +12 25380289 COSM1166779 C T . . GENE=KRAS;STRAND=-;CDS=c.169G>A;AA=p.D57N;CNT=1 +12 25380289 COSM1212769 C T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.169G>A;AA=p.D57N;CNT=1 +12 25398248 COSM1152501 A T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.71T>A;AA=p.I24N;CNT=1 +12 25398248 COSM87313 A T . . GENE=KRAS;STRAND=-;CDS=c.71T>A;AA=p.I24N;CNT=1 +12 25398255 COSM543 G T . . GENE=KRAS;STRAND=-;CDS=c.64C>A;AA=p.Q22K;CNT=1 +12 25398260 COSM1152502 G C . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.59C>G;AA=p.T20R;CNT=1 +12 25398260 COSM938161 G C . . GENE=KRAS;STRAND=-;CDS=c.59C>G;AA=p.T20R;CNT=1 +12 25398262 COSM20818 C A . . GENE=KRAS;STRAND=-;CDS=c.57G>T;AA=p.L19F;CNT=1 +12 25398262 COSM1212766 C A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.57G>T;AA=p.L19F;CNT=1 +12 25398279 COSM12721 CGC CAA . . GENE=KRAS;STRAND=-;CDS=c.38_39GC>TT;AA=p.G13V;CNT=1 +12 25398280 COSM536 G A . . GENE=KRAS;STRAND=-;CDS=c.39C>T;AA=p.G13G;CNT=1 +12 25398280 COSM1152503 G A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.39C>T;AA=p.G13G;CNT=1 +12 25398281 COSM534 C A . . GENE=KRAS;STRAND=-;CDS=c.38G>T;AA=p.G13V;CNT=1 +12 25398281 COSM1140132 C T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.38G>A;AA=p.G13D;CNT=14 +12 25398281 COSM532 C T . . GENE=KRAS;STRAND=-;CDS=c.38G>A;AA=p.G13D;CNT=38 +12 25398281 COSM1152504 C A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.38G>T;AA=p.G13V;CNT=1 +12 25398282 COSM1152505 C A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.37G>T;AA=p.G13C;CNT=3 +12 25398282 COSM527 C A . . GENE=KRAS;STRAND=-;CDS=c.37G>T;AA=p.G13C;CNT=6 +12 25398283 COSM1159170 A C . . GENE=KRAS;STRAND=-;CDS=c.36T>G;AA=p.G12G;CNT=2 +12 25398283 COSM1159169 A C . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.36T>G;AA=p.G12G;CNT=2 +12 25398283 COSM512 ACC AAA . . GENE=KRAS;STRAND=-;CDS=c.34_35GG>TT;AA=p.G12F;CNT=3 +12 25398283 COSM1140135 ACC AAA . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.34_35GG>TT;AA=p.G12F;CNT=2 +12 25398284 COSM522 C G . . GENE=KRAS;STRAND=-;CDS=c.35G>C;AA=p.G12A;CNT=19 +12 25398284 COSM520 C A . . GENE=KRAS;STRAND=-;CDS=c.35G>T;AA=p.G12V;CNT=126 +12 25398284 COSM521 C T . . GENE=KRAS;STRAND=-;CDS=c.35G>A;AA=p.G12D;CNT=110 +12 25398284 COSM1140134 C G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.35G>C;AA=p.G12A;CNT=12 +12 25398284 COSM1140133 C A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.35G>T;AA=p.G12V;CNT=86 +12 25398284 COSM1135366 C T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.35G>A;AA=p.G12D;CNT=69 +12 25398284 COSM394409 CCA CTA . . GENE=KRAS;STRAND=-;CDS=c.33_34TG>TA;AA=p.A11>?;CNT=1 +12 25398285 COSM517 C T . . GENE=KRAS;STRAND=-;CDS=c.34G>A;AA=p.G12S;CNT=9 +12 25398285 COSM1157797 C G . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.34G>C;AA=p.G12R;CNT=19 +12 25398285 COSM1152506 C T . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.34G>A;AA=p.G12S;CNT=5 +12 25398285 COSM518 C G . . GENE=KRAS;STRAND=-;CDS=c.34G>C;AA=p.G12R;CNT=26 +12 25398285 COSM1140136 C A . . GENE=KRAS_ENST00000256078;STRAND=-;CDS=c.34G>T;AA=p.G12C;CNT=41 +12 25398285 COSM516 C A . . GENE=KRAS;STRAND=-;CDS=c.34G>T;AA=p.G12C;CNT=73 +12 112888161 COSM314576 T C . . GENE=PTPN11;STRAND=+;CDS=c.177T>C;AA=p.T59T;CNT=1 +12 112888191 COSM201195 G T . . GENE=PTPN11;STRAND=+;CDS=c.207G>T;AA=p.E69D;CNT=1 +12 112888199 COSM13015 C T . . GENE=PTPN11;STRAND=+;CDS=c.215C>T;AA=p.A72V;CNT=1 +12 112888210 COSM13000 G A . . GENE=PTPN11;STRAND=+;CDS=c.226G>A;AA=p.E76K;CNT=1 +12 112888211 COSM13017 A G . . GENE=PTPN11;STRAND=+;CDS=c.227A>G;AA=p.E76G;CNT=1 +12 112926884 COSM13020 T C . . GENE=PTPN11;STRAND=+;CDS=c.1504T>C;AA=p.S502P;CNT=1 +12 112926888 COSM14271 G T . . GENE=PTPN11;STRAND=+;CDS=c.1508G>T;AA=p.G503V;CNT=1 +12 112926889 COSM397442 G T . . GENE=PTPN11;STRAND=+;CDS=c.1509G>T;AA=p.G503G;CNT=1 +12 112926942 COSM353792 A T . . GENE=PTPN11;STRAND=+;CDS=c.1562A>T;AA=p.Y521F;CNT=1 +12 121431482 COSM24911 G A . . GENE=HNF1A;STRAND=+;CDS=c.686G>A;AA=p.R229Q;CNT=1 +12 121431484 COSM251348 GAGACGCTAGTGGAGGAGTGCAATAGGTACAA G . . GENE=HNF1A;STRAND=+;CDS=c.689_713+6del31;AA=p.?;CNT=1 +12 121432067 COSM24920 C A . . GENE=HNF1A;STRAND=+;CDS=c.814C>A;AA=p.R272S;CNT=1 +12 121432110 COSM394948 A T . . GENE=HNF1A;STRAND=+;CDS=c.857A>T;AA=p.Y286F;CNT=1 +12 121432114 COSM202412 C T . . GENE=HNF1A;STRAND=+;CDS=c.861C>T;AA=p.S287S;CNT=1 +13 28592641 COSM784 T A . . GENE=FLT3;STRAND=-;CDS=c.2504A>T;AA=p.D835V;CNT=1 +13 28592642 COSM785 C G . . GENE=FLT3;STRAND=-;CDS=c.2503G>C;AA=p.D835H;CNT=2 +13 28592642 COSM783 C A . . GENE=FLT3;STRAND=-;CDS=c.2503G>T;AA=p.D835Y;CNT=3 +13 28592689 COSM330266 A G . . GENE=FLT3;STRAND=-;CDS=c.2456T>C;AA=p.V819A;CNT=1 +13 28602308 COSM550913 G T . . GENE=FLT3;STRAND=-;CDS=c.2053+7C>A;AA=p.?;CNT=1 +13 28602339 COSM161098 G A . . GENE=FLT3;STRAND=-;CDS=c.2029C>T;AA=p.L677L;CNT=1 +13 28602365 COSM385120 A G . . GENE=FLT3;STRAND=-;CDS=c.2003T>C;AA=p.L668P;CNT=1 +13 28602366 COSM550912 G A . . GENE=FLT3;STRAND=-;CDS=c.2002C>T;AA=p.L668L;CNT=1 +13 28602427 COSM550911 T A . . GENE=FLT3;STRAND=-;CDS=c.1943-2A>T;AA=p.?;CNT=1 +13 28608256 COSM158605 A ATCATATTCATATTCATATTCATAT . . GENE=FLT3;STRAND=-;CDS=c.1799_1800ins24;AA=p.Y599_D600insEYEYEYEY;CNT=2 +13 28608258 COSM158603 C CGGCGATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGG . . GENE=FLT3;STRAND=-;CDS=c.1797_1798ins57;AA=p.Y599_D600ins19;CNT=2 +13 28608273 COSM158601 T TGAAATCAACGTAGAAGTACTCATTATCTGA . . GENE=FLT3;STRAND=-;CDS=c.1782_1783ins30;AA=p.F594_R595ins10;CNT=2 +13 28610128 COSM335014 C A . . GENE=FLT3;STRAND=-;CDS=c.1362G>T;AA=p.S454S;CNT=1 +13 28610129 COSM696841 G A . . GENE=FLT3;STRAND=-;CDS=c.1361C>T;AA=p.S454L;CNT=1 +13 48919214 COSM326324 A T . . GENE=RB1;STRAND=+;CDS=c.381-2A>T;AA=p.?;CNT=1 +13 48919285 COSM147686 A T . . GENE=RB1;STRAND=+;CDS=c.450A>T;AA=p.R150S;CNT=1 +13 48919299 COSM391280 AT A . . GENE=RB1;STRAND=+;CDS=c.465delT;AA=p.Y155fs*1;CNT=1 +13 48923135 COSM317954 TG T . . GENE=RB1;STRAND=+;CDS=c.584delG;AA=p.W195fs*1;CNT=1 +13 48923137 COSM214151 G A . . GENE=RB1;STRAND=+;CDS=c.585G>A;AA=p.W195*;CNT=1 +13 48942688 COSM166169 AAAAGT A . . GENE=RB1;STRAND=+;CDS=c.1076_1080delAAAGT;AA=p.S360fs*2;CNT=1 +13 48942718 COSM318381 AT A . . GENE=RB1;STRAND=+;CDS=c.1106delT;AA=p.P370fs*10;CNT=1 +13 48955539 COSM69074 GATGTGAACATCGAATC G . . GENE=RB1;STRAND=+;CDS=c.1656_1671del16;AA=p.C553fs*53;CNT=1 +13 49027127 COSM347540 A G . . GENE=RB1;STRAND=+;CDS=c.1696-2A>G;AA=p.?;CNT=2 +13 49027127 COSM1152656 A G . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.1696-2A>G;AA=p.?;CNT=1 +13 49027133 COSM13118 C A . . GENE=RB1;STRAND=+;CDS=c.1700C>A;AA=p.S567*;CNT=1 +13 49027183 COSM1152657 G T . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.1750G>T;AA=p.D584Y;CNT=1 +13 49027183 COSM947798 G T . . GENE=RB1;STRAND=+;CDS=c.1750G>T;AA=p.D584Y;CNT=1 +13 49027248 COSM1133428 G A . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.1814+1G>A;AA=p.?;CNT=1 +13 49027248 COSM416348 G A . . GENE=RB1;STRAND=+;CDS=c.1814+1G>A;AA=p.?;CNT=1 +13 49033833 COSM212940 T C . . GENE=RB1;STRAND=+;CDS=c.1970T>C;AA=p.L657P;CNT=1 +13 49033853 COSM270006 A G . . GENE=RB1;STRAND=+;CDS=c.1990A>G;AA=p.T664A;CNT=1 +13 49033857 COSM326321 T G . . GENE=RB1;STRAND=+;CDS=c.1994T>G;AA=p.L665R;CNT=1 +13 49033916 COSM13117 C T . . GENE=RB1;STRAND=+;CDS=c.2053C>T;AA=p.Q685*;CNT=1 +13 49033946 COSM288406 A G . . GENE=RB1;STRAND=+;CDS=c.2083A>G;AA=p.M695V;CNT=1 +13 49033954 COSM1140401 C G . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.2091C>G;AA=p.D697E;CNT=1 +13 49033954 COSM551466 C G . . GENE=RB1;STRAND=+;CDS=c.2091C>G;AA=p.D697E;CNT=1 +13 49033955 COSM49018 A T . . GENE=RB1;STRAND=+;CDS=c.2092A>T;AA=p.R698W;CNT=1 +13 49033964 COSM214511 GACCAAGTAAGAAA G . . GENE=RB1;STRAND=+;CDS=c.2102_2106+8delACCAAgtaagaaa;AA=p.?;CNT=1 +13 49033967 COSM76180 C A . . GENE=RB1;STRAND=+;CDS=c.2104C>A;AA=p.Q702K;CNT=1 +13 49033970 COSM317962 G T . . GENE=RB1;STRAND=+;CDS=c.2106+1G>T;AA=p.?;CNT=1 +13 49033970 COSM323003 G A . . GENE=RB1;STRAND=+;CDS=c.2106+1G>A;AA=p.?;CNT=1 +13 49037867 COSM190077 A T . . GENE=RB1;STRAND=+;CDS=c.2107A>T;AA=p.I703F;CNT=1 +13 49037872 COSM318368 GATGTGTTCC G . . GENE=RB1;STRAND=+;CDS=c.2113_2121delATGTGTTCC;AA=p.C706_M708delCSM;CNT=1 +13 49037877 COSM883 G T . . GENE=RB1;STRAND=+;CDS=c.2117G>T;AA=p.C706F;CNT=2 +13 49037933 COSM392224 G GN . . GENE=RB1;STRAND=+;CDS=c.2173_2174insTT;AA=p.T726fs*1;CNT=1 +13 49037946 COSM318377 AG A . . GENE=RB1;STRAND=+;CDS=c.2187delG;AA=p.D730fs*14;CNT=1 +13 49039132 COSM317963 A T . . GENE=RB1;STRAND=+;CDS=c.2212-2A>T;AA=p.?;CNT=1 +13 49039136 COSM314700 A G . . GENE=RB1;STRAND=+;CDS=c.2214A>G;AA=p.T738T;CNT=1 +13 49039145 COSM1192936 TGTT TATG . . GENE=RB1;STRAND=+;CDS=c.2224_2226GTT>ATG;AA=p.V742M;CNT=1 +13 49039145 COSM1192935 TGTT TATG . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.2224_2226GTT>ATG;AA=p.V742M;CNT=1 +13 49039161 COSM212665 G T . . GENE=RB1;STRAND=+;CDS=c.2239G>T;AA=p.E747*;CNT=1 +13 49039189 COSM1140402 A G . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.2267A>G;AA=p.Y756C;CNT=1 +13 49039189 COSM551465 A G . . GENE=RB1;STRAND=+;CDS=c.2267A>G;AA=p.Y756C;CNT=1 +13 49039206 COSM947804 C T . . GENE=RB1;STRAND=+;CDS=c.2284C>T;AA=p.Q762*;CNT=1 +13 49039206 COSM1152658 C T . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.2284C>T;AA=p.Q762*;CNT=1 +13 49039236 COSM348849 G T . . GENE=RB1;STRAND=+;CDS=c.2314G>T;AA=p.A772S;CNT=1 +13 49039250 COSM696474 A T . . GENE=RB1;STRAND=+;CDS=c.2325+3A>T;AA=p.?;CNT=1 +13 49039250 COSM1147225 A T . . GENE=RB1_ENST00000267163;STRAND=+;CDS=c.2325+3A>T;AA=p.?;CNT=1 +14 105246445 COSM93893 A C . . GENE=AKT1;STRAND=-;CDS=c.155T>G;AA=p.L52R;CNT=1 +14 105246482 COSM469704 C T . . GENE=AKT1;STRAND=-;CDS=c.118G>A;AA=p.E40K;CNT=1 +14 105246551 COSM33765 C T . . GENE=AKT1;STRAND=-;CDS=c.49G>A;AA=p.E17K;CNT=14 +16 68835620 COSM704381 C T . . GENE=CDH1;STRAND=+;CDS=c.211C>T;AA=p.L71F;CNT=1 +16 68835640 COSM558825 G T . . GENE=CDH1;STRAND=+;CDS=c.231G>T;AA=p.V77V;CNT=1 +16 68835693 COSM972774 A T . . GENE=CDH1;STRAND=+;CDS=c.284A>T;AA=p.Q95L;CNT=1 +16 68835711 COSM194599 A G . . GENE=CDH1;STRAND=+;CDS=c.302A>G;AA=p.Y101C;CNT=1 +16 68835746 COSM166000 AAAGTCACGCTG A . . GENE=CDH1;STRAND=+;CDS=c.338_348del11;AA=p.V114fs*50;CNT=1 +16 68846122 COSM294225 G A . . GENE=CDH1;STRAND=+;CDS=c.1093G>A;AA=p.V365I;CNT=1 +16 68846165 COSM1128899 C T . . GENE=CDH1;STRAND=+;CDS=c.1136C>T;AA=p.T379M;CNT=1 +16 68847285 COSM972788 G A . . GENE=CDH1;STRAND=+;CDS=c.1207G>A;AA=p.A403T;CNT=1 +16 68847292 COSM165999 ATACCCCAGCGTGGGAGGCTG A . . GENE=CDH1;STRAND=+;CDS=c.1215_1234del20;AA=p.T406fs*6;CNT=1 +16 68847302 COSM194601 G A . . GENE=CDH1;STRAND=+;CDS=c.1224G>A;AA=p.A408A;CNT=1 +16 68847330 COSM398950 G A . . GENE=CDH1;STRAND=+;CDS=c.1252G>A;AA=p.D418N;CNT=1 +16 68847375 COSM239247 G A . . GENE=CDH1;STRAND=+;CDS=c.1297G>A;AA=p.D433N;CNT=1 +16 68847399 COSM20829 G C . . GENE=CDH1;STRAND=+;CDS=c.1320+1G>C;AA=p.?;CNT=1 +17 7573981 COSM707071 TCC TAA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1044_1045GG>TT;AA=p.L348_E349>F*;CNT=1 +17 7573981 COSM707070 TCC TAA . . GENE=TP53;STRAND=-;CDS=c.1044_1045GG>TT;AA=p.L348_E349>F*;CNT=1 +17 7573982 COSM140784 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1045G>T;AA=p.E349*;CNT=4 +17 7573982 COSM10770 C A . . GENE=TP53;STRAND=-;CDS=c.1045G>T;AA=p.E349*;CNT=5 +17 7573983 COSM46348 C A . . GENE=TP53;STRAND=-;CDS=c.1044G>T;AA=p.L348F;CNT=2 +17 7573983 COSM707069 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1044G>T;AA=p.L348F;CNT=1 +17 7573984 COSM69193 A AAGGCCTT . . GENE=TP53;STRAND=-;CDS=c.1042_1043insAAGGCCT;AA=p.L348fs*1;CNT=1 +17 7573988 COSM45717 C T . . GENE=TP53;STRAND=-;CDS=c.1039G>A;AA=p.A347T;CNT=1 +17 7573988 COSM1191612 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1039G>A;AA=p.A347T;CNT=1 +17 7573993 COSM1169350 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1034A>T;AA=p.N345I;CNT=1 +17 7573993 COSM1169349 T A . . GENE=TP53;STRAND=-;CDS=c.1034A>T;AA=p.N345I;CNT=1 +17 7573994 COSM69016 TC T . . GENE=TP53;STRAND=-;CDS=c.1032delG;AA=p.N345fs*25;CNT=1 +17 7573996 COSM46303 A C . . GENE=TP53;STRAND=-;CDS=c.1031T>G;AA=p.L344R;CNT=1 +17 7573996 COSM323924 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1031T>G;AA=p.L344R;CNT=1 +17 7574000 COSM308326 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1027G>T;AA=p.E343*;CNT=3 +17 7574000 COSM11078 C A . . GENE=TP53;STRAND=-;CDS=c.1027G>T;AA=p.E343*;CNT=3 +17 7574002 COSM45276 C G . . GENE=TP53;STRAND=-;CDS=c.1025G>C;AA=p.R342P;CNT=1 +17 7574002 COSM437468 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1025G>C;AA=p.R342P;CNT=1 +17 7574002 COSM18597 CG C . . GENE=TP53;STRAND=-;CDS=c.1024delC;AA=p.R342fs*3;CNT=1 +17 7574002 COSM128665 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1024delC;AA=p.R342fs*3;CNT=1 +17 7574003 COSM99721 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1024C>T;AA=p.R342*;CNT=12 +17 7574003 COSM11073 G A . . GENE=TP53;STRAND=-;CDS=c.1024C>T;AA=p.R342*;CNT=15 +17 7574003 COSM306101 G GTTCAGCTCTC . . GENE=TP53;STRAND=-;CDS=c.1023_1024ins10;AA=p.R342fs*3;CNT=1 +17 7574003 COSM306102 G GTTCAGCTCTC . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1023_1024ins10;AA=p.R342fs*3;CNT=1 +17 7574003 COSM43795 GG G . . GENE=TP53;STRAND=-;CDS=c.1023delC;AA=p.R342fs*3;CNT=1 +17 7574003 COSM241992 GG G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1023delC;AA=p.R342fs*3;CNT=1 +17 7574009 COSM84370 T C . . GENE=TP53;STRAND=-;CDS=c.1018A>G;AA=p.M340V;CNT=1 +17 7574009 COSM85579 TCTCG T . . GENE=TP53;STRAND=-;CDS=c.1014_1017delCGAG;AA=p.F338fs*6;CNT=1 +17 7574010 COSM85580 CTCG C . . GENE=TP53;STRAND=-;CDS=c.1014_1016delCGA;AA=p.F338_E339>L;CNT=1 +17 7574012 COSM214290 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1015G>T;AA=p.E339*;CNT=1 +17 7574012 COSM11286 C A . . GENE=TP53;STRAND=-;CDS=c.1015G>T;AA=p.E339*;CNT=1 +17 7574017 COSM131485 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1010G>A;AA=p.R337H;CNT=1 +17 7574017 COSM378685 C G . . GENE=TP53;STRAND=-;CDS=c.1010G>C;AA=p.R337P;CNT=1 +17 7574017 COSM220135 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1010G>T;AA=p.R337L;CNT=7 +17 7574017 COSM378686 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1010G>C;AA=p.R337P;CNT=1 +17 7574017 COSM43882 C T . . GENE=TP53;STRAND=-;CDS=c.1010G>A;AA=p.R337H;CNT=1 +17 7574017 COSM11411 C A . . GENE=TP53;STRAND=-;CDS=c.1010G>T;AA=p.R337L;CNT=7 +17 7574017 COSM111628 CG C . . GENE=TP53;STRAND=-;CDS=c.1009delC;AA=p.R337fs*8;CNT=1 +17 7574017 COSM111629 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1009delC;AA=p.R337fs*8;CNT=1 +17 7574018 COSM11071 G A . . GENE=TP53;STRAND=-;CDS=c.1009C>T;AA=p.R337C;CNT=3 +17 7574018 COSM117591 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1009C>T;AA=p.R337C;CNT=3 +17 7574022 COSM295248 AC A . . GENE=TP53;STRAND=-;CDS=c.1004delG;AA=p.R335fs*10;CNT=1 +17 7574022 COSM295249 AC A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1004delG;AA=p.R335fs*10;CNT=1 +17 7574023 COSM288629 C CT . . GENE=TP53;STRAND=-;CDS=c.1003_1004insA;AA=p.R335fs*2;CNT=1 +17 7574023 COSM288630 C CT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1003_1004insA;AA=p.R335fs*2;CNT=1 +17 7574026 COSM330688 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1001G>C;AA=p.G334A;CNT=1 +17 7574026 COSM330687 C G . . GENE=TP53;STRAND=-;CDS=c.1001G>C;AA=p.G334A;CNT=1 +17 7574026 COSM323935 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.1001G>T;AA=p.G334V;CNT=2 +17 7574026 COSM11514 C A . . GENE=TP53;STRAND=-;CDS=c.1001G>T;AA=p.G334V;CNT=2 +17 7574029 COSM69084 CG C . . GENE=TP53;STRAND=-;CDS=c.997delC;AA=p.R333fs*12;CNT=2 +17 7574029 COSM437469 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.997delC;AA=p.R333fs*12;CNT=1 +17 7574034 COSM984869 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.994-1G>C;AA=p.?;CNT=1 +17 7574034 COSM562343 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.994-1G>T;AA=p.?;CNT=1 +17 7574034 COSM49007 C A . . GENE=TP53;STRAND=-;CDS=c.994-1G>T;AA=p.?;CNT=1 +17 7574034 COSM69404 C T . . GENE=TP53;STRAND=-;CDS=c.994-1G>A;AA=p.?;CNT=1 +17 7574034 COSM13745 C G . . GENE=TP53;STRAND=-;CDS=c.994-1G>C;AA=p.?;CNT=1 +17 7574035 COSM318155 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.994-2A>G;AA=p.?;CNT=1 +17 7574035 COSM87027 T C . . GENE=TP53;STRAND=-;CDS=c.994-2A>G;AA=p.?;CNT=1 +17 7577018 COSM44143 C T . . GENE=TP53;STRAND=-;CDS=c.919+1G>A;AA=p.?;CNT=4 +17 7577018 COSM1230104 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.919+1G>C;AA=p.?;CNT=1 +17 7577018 COSM213111 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.919+1G>A;AA=p.?;CNT=3 +17 7577018 COSM13585 C G . . GENE=TP53;STRAND=-;CDS=c.919+1G>C;AA=p.?;CNT=1 +17 7577018 COSM111649 CCT C . . GENE=TP53;STRAND=-;CDS=c.918_919delAG;AA=p.A307fs*29;CNT=1 +17 7577018 COSM111650 CCT C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.918_919delAG;AA=p.A307fs*29;CNT=1 +17 7577022 COSM10663 G A . . GENE=TP53;STRAND=-;CDS=c.916C>T;AA=p.R306*;CNT=18 +17 7577022 COSM99947 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.916C>T;AA=p.R306*;CNT=11 +17 7577025 COSM43773 T A . . GENE=TP53;STRAND=-;CDS=c.913A>T;AA=p.K305*;CNT=1 +17 7577025 COSM99951 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.913A>T;AA=p.K305*;CNT=1 +17 7577046 COSM10710 C A . . GENE=TP53;STRAND=-;CDS=c.892G>T;AA=p.E298*;CNT=5 +17 7577046 COSM121080 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.892G>T;AA=p.E298*;CNT=5 +17 7577057 COSM6621 TC T . . GENE=TP53;STRAND=-;CDS=c.880delG;AA=p.E294fs*51;CNT=1 +17 7577057 COSM318363 TC T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.880delG;AA=p.E294fs*51;CNT=1 +17 7577058 COSM10856 C A . . GENE=TP53;STRAND=-;CDS=c.880G>T;AA=p.E294*;CNT=6 +17 7577058 COSM126981 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.880G>T;AA=p.E294*;CNT=5 +17 7577064 COSM44894 T A . . GENE=TP53;STRAND=-;CDS=c.874A>T;AA=p.K292*;CNT=1 +17 7577064 COSM1172458 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.874A>T;AA=p.K292*;CNT=1 +17 7577064 COSM297085 TCTTGCGG T . . GENE=TP53;STRAND=-;CDS=c.867_873delCCGCAAG;AA=p.R290fs*53;CNT=1 +17 7577064 COSM297086 TCTTGCGG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.867_873delCCGCAAG;AA=p.R290fs*53;CNT=1 +17 7577070 COSM1167879 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.868C>T;AA=p.R290C;CNT=1 +17 7577070 COSM45679 G A . . GENE=TP53;STRAND=-;CDS=c.868C>T;AA=p.R290C;CNT=1 +17 7577071 COSM1158423 GA G . . GENE=TP53;STRAND=-;CDS=c.866delT;AA=p.L289fs*56;CNT=1 +17 7577071 COSM1158424 GA G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.866delT;AA=p.L289fs*56;CNT=1 +17 7577075 COSM111986 T TT . . GENE=TP53;STRAND=-;CDS=c.862_863insA;AA=p.N288fs*18;CNT=1 +17 7577075 COSM111987 T TT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.862_863insA;AA=p.N288fs*18;CNT=1 +17 7577079 COSM214243 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.859G>T;AA=p.E287*;CNT=2 +17 7577079 COSM44133 C A . . GENE=TP53;STRAND=-;CDS=c.859G>T;AA=p.E287*;CNT=2 +17 7577081 COSM43565 T C . . GENE=TP53;STRAND=-;CDS=c.857A>G;AA=p.E286G;CNT=2 +17 7577081 COSM288255 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.857A>G;AA=p.E286G;CNT=2 +17 7577081 COSM341111 TCC TTA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.855_856GG>TA;AA=p.E285>?;CNT=1 +17 7577081 COSM341110 TCC TTA . . GENE=TP53;STRAND=-;CDS=c.855_856GG>TA;AA=p.E285_E286>DK;CNT=1 +17 7577082 COSM318163 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.856G>T;AA=p.E286*;CNT=4 +17 7577082 COSM99924 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.856G>A;AA=p.E286K;CNT=4 +17 7577082 COSM10726 C T . . GENE=TP53;STRAND=-;CDS=c.856G>A;AA=p.E286K;CNT=5 +17 7577082 COSM43919 C A . . GENE=TP53;STRAND=-;CDS=c.856G>T;AA=p.E286*;CNT=4 +17 7577085 COSM44388 C A . . GENE=TP53;STRAND=-;CDS=c.853G>T;AA=p.E285*;CNT=2 +17 7577085 COSM137087 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.853G>A;AA=p.E285K;CNT=4 +17 7577085 COSM10722 C T . . GENE=TP53;STRAND=-;CDS=c.853G>A;AA=p.E285K;CNT=4 +17 7577085 COSM254990 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.853G>T;AA=p.E285*;CNT=2 +17 7577087 COSM69017 GT G . . GENE=TP53;STRAND=-;CDS=c.850delA;AA=p.T284fs*61;CNT=1 +17 7577088 COSM707066 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.850A>C;AA=p.T284P;CNT=1 +17 7577088 COSM44352 T G . . GENE=TP53;STRAND=-;CDS=c.850A>C;AA=p.T284P;CNT=1 +17 7577090 COSM10743 C G . . GENE=TP53;STRAND=-;CDS=c.848G>C;AA=p.R283P;CNT=3 +17 7577090 COSM99941 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.848G>C;AA=p.R283P;CNT=3 +17 7577090 COSM111954 C CA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.847_848insT;AA=p.R283fs*23;CNT=1 +17 7577090 COSM111953 C CA . . GENE=TP53;STRAND=-;CDS=c.847_848insT;AA=p.R283fs*23;CNT=1 +17 7577091 COSM10911 G A . . GENE=TP53;STRAND=-;CDS=c.847C>T;AA=p.R283C;CNT=1 +17 7577091 COSM707064 GCC GGT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.845_846GG>AC;AA=p.R282H;CNT=1 +17 7577091 COSM707063 GCC GGT . . GENE=TP53;STRAND=-;CDS=c.845_846GG>AC;AA=p.R282H;CNT=1 +17 7577092 COSM707065 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.846G>C;AA=p.R282R;CNT=1 +17 7577092 COSM43561 C G . . GENE=TP53;STRAND=-;CDS=c.846G>C;AA=p.R282R;CNT=1 +17 7577093 COSM99936 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.845G>A;AA=p.R282Q;CNT=2 +17 7577093 COSM44306 C G . . GENE=TP53;STRAND=-;CDS=c.845G>C;AA=p.R282P;CNT=1 +17 7577093 COSM44338 C T . . GENE=TP53;STRAND=-;CDS=c.845G>A;AA=p.R282Q;CNT=2 +17 7577093 COSM117157 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.845G>C;AA=p.R282P;CNT=1 +17 7577093 COSM112007 C CG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.844_845insC;AA=p.R282fs*24;CNT=1 +17 7577093 COSM112006 C CG . . GENE=TP53;STRAND=-;CDS=c.844_845insC;AA=p.R282fs*24;CNT=1 +17 7577094 COSM99934 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.844C>G;AA=p.R282G;CNT=2 +17 7577094 COSM99925 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.844C>T;AA=p.R282W;CNT=16 +17 7577094 COSM10704 G A . . GENE=TP53;STRAND=-;CDS=c.844C>T;AA=p.R282W;CNT=19 +17 7577094 COSM10992 G C . . GENE=TP53;STRAND=-;CDS=c.844C>G;AA=p.R282G;CNT=2 +17 7577095 COSM43906 G T . . GENE=TP53;STRAND=-;CDS=c.843C>A;AA=p.D281E;CNT=1 +17 7577095 COSM562342 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.843C>A;AA=p.D281E;CNT=1 +17 7577096 COSM45729 T A . . GENE=TP53;STRAND=-;CDS=c.842A>T;AA=p.D281V;CNT=1 +17 7577096 COSM11232 T C . . GENE=TP53;STRAND=-;CDS=c.842A>G;AA=p.D281G;CNT=1 +17 7577096 COSM562341 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.842A>T;AA=p.D281V;CNT=1 +17 7577097 COSM10943 C G . . GENE=TP53;STRAND=-;CDS=c.841G>C;AA=p.D281H;CNT=2 +17 7577097 COSM1158315 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.841G>C;AA=p.D281H;CNT=1 +17 7577097 COSM214193 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.841G>T;AA=p.D281Y;CNT=5 +17 7577097 COSM11516 C A . . GENE=TP53;STRAND=-;CDS=c.841G>T;AA=p.D281Y;CNT=5 +17 7577097 COSM146336 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.841G>A;AA=p.D281N;CNT=2 +17 7577097 COSM43596 C T . . GENE=TP53;STRAND=-;CDS=c.841G>A;AA=p.D281N;CNT=2 +17 7577099 COSM11287 C A . . GENE=TP53;STRAND=-;CDS=c.839G>T;AA=p.R280I;CNT=4 +17 7577099 COSM254987 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.839G>C;AA=p.R280T;CNT=4 +17 7577099 COSM10728 C T . . GENE=TP53;STRAND=-;CDS=c.839G>A;AA=p.R280K;CNT=2 +17 7577099 COSM10724 C G . . GENE=TP53;STRAND=-;CDS=c.839G>C;AA=p.R280T;CNT=4 +17 7577099 COSM129830 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.839G>A;AA=p.R280K;CNT=2 +17 7577099 COSM562340 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.839G>T;AA=p.R280I;CNT=3 +17 7577100 COSM562339 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.838A>G;AA=p.R280G;CNT=1 +17 7577100 COSM11123 T C . . GENE=TP53;STRAND=-;CDS=c.838A>G;AA=p.R280G;CNT=1 +17 7577102 COSM43714 C T . . GENE=TP53;STRAND=-;CDS=c.836G>A;AA=p.G279E;CNT=1 +17 7577103 COSM46298 C G . . GENE=TP53;STRAND=-;CDS=c.835G>C;AA=p.G279R;CNT=1 +17 7577103 COSM417973 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.835G>C;AA=p.G279R;CNT=1 +17 7577105 COSM43755 G T . . GENE=TP53;STRAND=-;CDS=c.833C>A;AA=p.P278H;CNT=3 +17 7577105 COSM300205 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.833C>G;AA=p.P278R;CNT=2 +17 7577105 COSM10863 G A . . GENE=TP53;STRAND=-;CDS=c.833C>T;AA=p.P278L;CNT=3 +17 7577105 COSM333585 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.833C>A;AA=p.P278H;CNT=2 +17 7577105 COSM129831 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.833C>T;AA=p.P278L;CNT=3 +17 7577105 COSM10887 G C . . GENE=TP53;STRAND=-;CDS=c.833C>G;AA=p.P278R;CNT=3 +17 7577106 COSM10814 G C . . GENE=TP53;STRAND=-;CDS=c.832C>G;AA=p.P278A;CNT=3 +17 7577106 COSM368635 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.832C>A;AA=p.P278T;CNT=2 +17 7577106 COSM43697 G T . . GENE=TP53;STRAND=-;CDS=c.832C>A;AA=p.P278T;CNT=2 +17 7577106 COSM99725 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.832C>G;AA=p.P278A;CNT=3 +17 7577106 COSM10939 G A . . GENE=TP53;STRAND=-;CDS=c.832C>T;AA=p.P278S;CNT=3 +17 7577106 COSM139044 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.832C>T;AA=p.P278S;CNT=3 +17 7577107 COSM44972 A T . . GENE=TP53;STRAND=-;CDS=c.831T>A;AA=p.C277*;CNT=1 +17 7577107 COSM417972 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.831T>A;AA=p.C277*;CNT=1 +17 7577108 COSM10749 C A . . GENE=TP53;STRAND=-;CDS=c.830G>T;AA=p.C277F;CNT=4 +17 7577108 COSM562338 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.830G>T;AA=p.C277F;CNT=3 +17 7577111 COSM393936 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.827C>A;AA=p.A276D;CNT=1 +17 7577111 COSM45268 G T . . GENE=TP53;STRAND=-;CDS=c.827C>A;AA=p.A276D;CNT=1 +17 7577112 COSM43663 C G . . GENE=TP53;STRAND=-;CDS=c.826G>C;AA=p.A276P;CNT=1 +17 7577114 COSM10893 C T . . GENE=TP53;STRAND=-;CDS=c.824G>A;AA=p.C275Y;CNT=6 +17 7577114 COSM45413 C G . . GENE=TP53;STRAND=-;CDS=c.824G>C;AA=p.C275S;CNT=1 +17 7577114 COSM1167915 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.824G>C;AA=p.C275S;CNT=1 +17 7577114 COSM165084 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.824G>A;AA=p.C275Y;CNT=4 +17 7577114 COSM10701 C A . . GENE=TP53;STRAND=-;CDS=c.824G>T;AA=p.C275F;CNT=2 +17 7577114 COSM99932 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.824G>T;AA=p.C275F;CNT=2 +17 7577117 COSM165076 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.821T>A;AA=p.V274D;CNT=1 +17 7577117 COSM43945 A C . . GENE=TP53;STRAND=-;CDS=c.821T>G;AA=p.V274G;CNT=2 +17 7577117 COSM131453 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.821T>C;AA=p.V274A;CNT=3 +17 7577117 COSM44448 A T . . GENE=TP53;STRAND=-;CDS=c.821T>A;AA=p.V274D;CNT=2 +17 7577117 COSM44393 A G . . GENE=TP53;STRAND=-;CDS=c.821T>C;AA=p.V274A;CNT=3 +17 7577117 COSM241993 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.821T>G;AA=p.V274G;CNT=1 +17 7577118 COSM44443 C G . . GENE=TP53;STRAND=-;CDS=c.820G>C;AA=p.V274L;CNT=1 +17 7577118 COSM10769 C A . . GENE=TP53;STRAND=-;CDS=c.820G>T;AA=p.V274F;CNT=3 +17 7577118 COSM165075 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.820G>T;AA=p.V274F;CNT=3 +17 7577118 COSM172146 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.820G>C;AA=p.V274L;CNT=1 +17 7577119 COSM304198 ACG A . . GENE=TP53;STRAND=-;CDS=c.817_818delCG;AA=p.R273fs*32;CNT=1 +17 7577119 COSM304199 ACG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.817_818delCG;AA=p.R273fs*32;CNT=1 +17 7577120 COSM165077 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.818G>C;AA=p.R273P;CNT=4 +17 7577120 COSM10660 C T . . GENE=TP53;STRAND=-;CDS=c.818G>A;AA=p.R273H;CNT=36 +17 7577120 COSM43896 C G . . GENE=TP53;STRAND=-;CDS=c.818G>C;AA=p.R273P;CNT=5 +17 7577120 COSM10779 C A . . GENE=TP53;STRAND=-;CDS=c.818G>T;AA=p.R273L;CNT=14 +17 7577120 COSM318169 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.818G>T;AA=p.R273L;CNT=9 +17 7577120 COSM99729 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.818G>A;AA=p.R273H;CNT=26 +17 7577120 COSM417969 CGC CTT . . GENE=TP53;STRAND=-;CDS=c.816_817GC>AA;AA=p.R273S;CNT=1 +17 7577120 COSM417970 CGC CTT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.816_817GC>AA;AA=p.V272>?;CNT=1 +17 7577121 COSM99933 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.817C>T;AA=p.R273C;CNT=25 +17 7577121 COSM10659 G A . . GENE=TP53;STRAND=-;CDS=c.817C>T;AA=p.R273C;CNT=32 +17 7577121 COSM43909 G T . . GENE=TP53;STRAND=-;CDS=c.817C>A;AA=p.R273S;CNT=2 +17 7577121 COSM417971 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.817C>A;AA=p.R273S;CNT=2 +17 7577122 COSM417968 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.816G>A;AA=p.V272V;CNT=1 +17 7577122 COSM44857 C T . . GENE=TP53;STRAND=-;CDS=c.816G>A;AA=p.V272V;CNT=1 +17 7577122 COSM376176 CAC CTT . . GENE=TP53;STRAND=-;CDS=c.814_815GT>AA;AA=p.V272K;CNT=1 +17 7577122 COSM376177 CAC CTT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.814_815GT>AA;AA=p.V272>?;CNT=1 +17 7577123 COSM562337 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.815T>G;AA=p.V272G;CNT=1 +17 7577123 COSM44870 A C . . GENE=TP53;STRAND=-;CDS=c.815T>G;AA=p.V272G;CNT=1 +17 7577123 COSM13421 AC A . . GENE=TP53;STRAND=-;CDS=c.814delG;AA=p.V272fs*73;CNT=1 +17 7577124 COSM212313 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.814G>T;AA=p.V272L;CNT=1 +17 7577124 COSM1177737 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.814G>C;AA=p.V272L;CNT=1 +17 7577124 COSM99950 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.814G>A;AA=p.V272M;CNT=5 +17 7577124 COSM45898 C G . . GENE=TP53;STRAND=-;CDS=c.814G>C;AA=p.V272L;CNT=1 +17 7577124 COSM10859 C A . . GENE=TP53;STRAND=-;CDS=c.814G>T;AA=p.V272L;CNT=1 +17 7577124 COSM10891 C T . . GENE=TP53;STRAND=-;CDS=c.814G>A;AA=p.V272M;CNT=7 +17 7577125 COSM214520 CT C . . GENE=TP53;STRAND=-;CDS=c.812delA;AA=p.E271fs*74;CNT=1 +17 7577125 COSM214521 CT C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.812delA;AA=p.E271fs*74;CNT=1 +17 7577127 COSM131516 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.811G>T;AA=p.E271*;CNT=2 +17 7577127 COSM43706 C G . . GENE=TP53;STRAND=-;CDS=c.811G>C;AA=p.E271Q;CNT=1 +17 7577127 COSM43750 C A . . GENE=TP53;STRAND=-;CDS=c.811G>T;AA=p.E271*;CNT=3 +17 7577127 COSM165082 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.811G>C;AA=p.E271Q;CNT=1 +17 7577127 COSM10719 C T . . GENE=TP53;STRAND=-;CDS=c.811G>A;AA=p.E271K;CNT=2 +17 7577127 COSM254988 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.811G>A;AA=p.E271K;CNT=2 +17 7577128 COSM45297 A C . . GENE=TP53;STRAND=-;CDS=c.810T>G;AA=p.F270L;CNT=1 +17 7577130 COSM44262 A G . . GENE=TP53;STRAND=-;CDS=c.808T>C;AA=p.F270L;CNT=1 +17 7577130 COSM165083 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.808T>C;AA=p.F270L;CNT=1 +17 7577130 COSM43809 A T . . GENE=TP53;STRAND=-;CDS=c.808T>A;AA=p.F270I;CNT=1 +17 7577130 COSM437484 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.808T>A;AA=p.F270I;CNT=1 +17 7577138 COSM11392 C G . . GENE=TP53;STRAND=-;CDS=c.800G>C;AA=p.R267P;CNT=2 +17 7577138 COSM707909 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.800G>C;AA=p.R267P;CNT=2 +17 7577138 COSM13165 C A . . GENE=TP53;STRAND=-;CDS=c.800G>T;AA=p.R267L;CNT=2 +17 7577138 COSM327262 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.800G>T;AA=p.R267L;CNT=2 +17 7577139 COSM179804 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.799C>T;AA=p.R267W;CNT=2 +17 7577139 COSM11183 G A . . GENE=TP53;STRAND=-;CDS=c.799C>T;AA=p.R267W;CNT=2 +17 7577141 COSM99952 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.797G>T;AA=p.G266V;CNT=7 +17 7577141 COSM216410 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.797G>A;AA=p.G266E;CNT=3 +17 7577141 COSM10867 C T . . GENE=TP53;STRAND=-;CDS=c.797G>A;AA=p.G266E;CNT=3 +17 7577141 COSM10958 C A . . GENE=TP53;STRAND=-;CDS=c.797G>T;AA=p.G266V;CNT=9 +17 7577142 COSM11205 C G . . GENE=TP53;STRAND=-;CDS=c.796G>C;AA=p.G266R;CNT=1 +17 7577142 COSM297539 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.796G>T;AA=p.G266*;CNT=1 +17 7577142 COSM10794 C T . . GENE=TP53;STRAND=-;CDS=c.796G>A;AA=p.G266R;CNT=2 +17 7577142 COSM318165 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.796G>C;AA=p.G266R;CNT=1 +17 7577142 COSM44891 C A . . GENE=TP53;STRAND=-;CDS=c.796G>T;AA=p.G266*;CNT=1 +17 7577144 COSM44092 A C . . GENE=TP53;STRAND=-;CDS=c.794T>G;AA=p.L265R;CNT=1 +17 7577144 COSM437485 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.794T>G;AA=p.L265R;CNT=1 +17 7577144 COSM11011 A G . . GENE=TP53;STRAND=-;CDS=c.794T>C;AA=p.L265P;CNT=1 +17 7577145 COSM69178 GT G . . GENE=TP53;STRAND=-;CDS=c.783-1_792delGTGGTAATCTA;AA=p.?;CNT=1 +17 7577146 COSM69217 T TAGATTACCACTACTC . . GENE=TP53;STRAND=-;CDS=c.791_792ins15;AA=p.L264_L265insSSGNL;CNT=1 +17 7577153 COSM11198 C A . . GENE=TP53;STRAND=-;CDS=c.785G>T;AA=p.G262V;CNT=6 +17 7577153 COSM216411 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.785G>T;AA=p.G262V;CNT=5 +17 7577156 COSM127199 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.783-1G>T;AA=p.?;CNT=4 +17 7577156 COSM6913 C A . . GENE=TP53;STRAND=-;CDS=c.783-1G>T;AA=p.?;CNT=4 +17 7577157 COSM1230105 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.783-2A>T;AA=p.?;CNT=1 +17 7577157 COSM45956 T A . . GENE=TP53;STRAND=-;CDS=c.783-2A>T;AA=p.?;CNT=1 +17 7577498 COSM44640 C A . . GENE=TP53;STRAND=-;CDS=c.782+1G>T;AA=p.?;CNT=2 +17 7577498 COSM473431 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.782+1G>T;AA=p.?;CNT=1 +17 7577498 COSM395657 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.782+1G>A;AA=p.?;CNT=1 +17 7577498 COSM43571 C T . . GENE=TP53;STRAND=-;CDS=c.782+1G>A;AA=p.?;CNT=2 +17 7577498 COSM395658 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.782+1G>A;AA=p.?;CNT=1 +17 7577498 COSM473430 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.782+1G>T;AA=p.?;CNT=1 +17 7577500 COSM45668 TG T . . GENE=TP53;STRAND=-;CDS=c.780delC;AA=p.S261fs*84;CNT=1 +17 7577504 COSM707904 GTC GAA . . GENE=TP53;STRAND=-;CDS=c.775_776GA>TT;AA=p.D259F;CNT=1 +17 7577504 COSM707905 GTC GAA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.775_776GA>TT;AA=p.D259F;CNT=1 +17 7577504 COSM707906 GTC GAA . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.775_776GA>TT;AA=p.D259F;CNT=1 +17 7577505 COSM707907 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.776A>T;AA=p.D259V;CNT=1 +17 7577505 COSM43724 T A . . GENE=TP53;STRAND=-;CDS=c.776A>T;AA=p.D259V;CNT=1 +17 7577505 COSM707908 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.776A>T;AA=p.D259V;CNT=1 +17 7577506 COSM707903 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.775G>T;AA=p.D259Y;CNT=1 +17 7577506 COSM11552 C A . . GENE=TP53;STRAND=-;CDS=c.775G>T;AA=p.D259Y;CNT=3 +17 7577506 COSM707902 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.775G>T;AA=p.D259Y;CNT=1 +17 7577509 COSM43568 C A . . GENE=TP53;STRAND=-;CDS=c.772G>T;AA=p.E258*;CNT=3 +17 7577509 COSM173137 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.772G>T;AA=p.E258*;CNT=3 +17 7577509 COSM173138 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.772G>T;AA=p.E258*;CNT=3 +17 7577511 COSM43530 A T . . GENE=TP53;STRAND=-;CDS=c.770T>A;AA=p.L257Q;CNT=3 +17 7577511 COSM1230108 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.770T>A;AA=p.L257Q;CNT=2 +17 7577511 COSM1230109 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.770T>A;AA=p.L257Q;CNT=2 +17 7577511 COSM1190904 AGTG A . . GENE=TP53;STRAND=-;CDS=c.767_769delCAC;AA=p.T256_L257>M;CNT=1 +17 7577511 COSM1190905 AGTG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.767_769delCAC;AA=p.T256_L257>M;CNT=1 +17 7577511 COSM1190906 AGTG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.767_769delCAC;AA=p.T256_L257>M;CNT=1 +17 7577513 COSM69134 TGTGATGATG T . . GENE=TP53;STRAND=-;CDS=c.759_767delCATCATCAC;AA=p.I254_T256delIIT;CNT=1 +17 7577513 COSM69135 TGTG T . . GENE=TP53;STRAND=-;CDS=c.765_767delCAC;AA=p.T256delT;CNT=2 +17 7577513 COSM1190907 TGTG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.765_767delCAC;AA=p.T256delT;CNT=1 +17 7577513 COSM1190908 TGTG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.765_767delCAC;AA=p.T256delT;CNT=1 +17 7577517 COSM437489 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.764T>G;AA=p.I255S;CNT=1 +17 7577517 COSM437488 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.764T>G;AA=p.I255S;CNT=1 +17 7577517 COSM10788 A C . . GENE=TP53;STRAND=-;CDS=c.764T>G;AA=p.I255S;CNT=1 +17 7577518 COSM220790 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.763A>T;AA=p.I255F;CNT=2 +17 7577518 COSM43651 T A . . GENE=TP53;STRAND=-;CDS=c.763A>T;AA=p.I255F;CNT=2 +17 7577518 COSM220791 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.763A>T;AA=p.I255F;CNT=2 +17 7577518 COSM45601 TGAT T . . GENE=TP53;STRAND=-;CDS=c.760_762delATC;AA=p.I255delI;CNT=1 +17 7577518 COSM1191147 TGAT T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.760_762delATC;AA=p.I255delI;CNT=1 +17 7577518 COSM1191148 TGAT T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.760_762delATC;AA=p.I255delI;CNT=1 +17 7577520 COSM45035 A C . . GENE=TP53;STRAND=-;CDS=c.761T>G;AA=p.I254S;CNT=1 +17 7577520 COSM1230107 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.761T>G;AA=p.I254S;CNT=1 +17 7577520 COSM1230106 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.761T>G;AA=p.I254S;CNT=1 +17 7577521 COSM307260 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.760A>G;AA=p.I254V;CNT=1 +17 7577521 COSM307259 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.760A>G;AA=p.I254V;CNT=1 +17 7577521 COSM44030 T C . . GENE=TP53;STRAND=-;CDS=c.760A>G;AA=p.I254V;CNT=1 +17 7577523 COSM307262 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.758C>A;AA=p.T253N;CNT=1 +17 7577523 COSM44993 G T . . GENE=TP53;STRAND=-;CDS=c.758C>A;AA=p.T253N;CNT=1 +17 7577523 COSM307261 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.758C>A;AA=p.T253N;CNT=1 +17 7577524 COSM44247 TGAG T . . GENE=TP53;STRAND=-;CDS=c.754_756delCTC;AA=p.L252delL;CNT=2 +17 7577524 COSM984891 TGAG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.754_756delCTC;AA=p.L252delL;CNT=2 +17 7577524 COSM984893 TGAG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.754_756delCTC;AA=p.L252delL;CNT=2 +17 7577526 COSM148174 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.755T>C;AA=p.L252P;CNT=1 +17 7577526 COSM44769 A G . . GENE=TP53;STRAND=-;CDS=c.755T>C;AA=p.L252P;CNT=1 +17 7577526 COSM148175 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.755T>C;AA=p.L252P;CNT=1 +17 7577529 COSM11374 A T . . GENE=TP53;STRAND=-;CDS=c.752T>A;AA=p.I251N;CNT=1 +17 7577529 COSM242660 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.752T>A;AA=p.I251N;CNT=1 +17 7577529 COSM43829 A C . . GENE=TP53;STRAND=-;CDS=c.752T>G;AA=p.I251S;CNT=1 +17 7577529 COSM242661 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.752T>A;AA=p.I251N;CNT=1 +17 7577530 COSM169049 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.751A>T;AA=p.I251F;CNT=1 +17 7577530 COSM169050 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.751A>T;AA=p.I251F;CNT=1 +17 7577530 COSM43967 T A . . GENE=TP53;STRAND=-;CDS=c.751A>T;AA=p.I251F;CNT=1 +17 7577532 COSM212254 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.749C>A;AA=p.P250H;CNT=1 +17 7577532 COSM44476 G T . . GENE=TP53;STRAND=-;CDS=c.749C>A;AA=p.P250H;CNT=1 +17 7577532 COSM212111 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.749C>T;AA=p.P250L;CNT=2 +17 7577532 COSM212255 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.749C>A;AA=p.P250H;CNT=1 +17 7577532 COSM212112 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.749C>T;AA=p.P250L;CNT=2 +17 7577532 COSM10771 G A . . GENE=TP53;STRAND=-;CDS=c.749C>T;AA=p.P250L;CNT=4 +17 7577534 COSM10785 C G . . GENE=TP53;STRAND=-;CDS=c.747G>C;AA=p.R249S;CNT=1 +17 7577534 COSM255317 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.747G>C;AA=p.R249S;CNT=1 +17 7577534 COSM131479 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.747G>T;AA=p.R249S;CNT=9 +17 7577534 COSM10817 C A . . GENE=TP53;STRAND=-;CDS=c.747G>T;AA=p.R249S;CNT=9 +17 7577534 COSM255318 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.747G>C;AA=p.R249S;CNT=1 +17 7577534 COSM131478 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.747G>T;AA=p.R249S;CNT=9 +17 7577535 COSM129833 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.746G>A;AA=p.R249K;CNT=1 +17 7577535 COSM375643 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.746G>C;AA=p.R249T;CNT=1 +17 7577535 COSM129832 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.746G>A;AA=p.R249K;CNT=1 +17 7577535 COSM44091 C T . . GENE=TP53;STRAND=-;CDS=c.746G>A;AA=p.R249K;CNT=1 +17 7577535 COSM375642 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.746G>C;AA=p.R249T;CNT=1 +17 7577535 COSM326724 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.746G>T;AA=p.R249M;CNT=4 +17 7577535 COSM43665 C G . . GENE=TP53;STRAND=-;CDS=c.746G>C;AA=p.R249T;CNT=1 +17 7577535 COSM326723 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.746G>T;AA=p.R249M;CNT=4 +17 7577535 COSM43871 C A . . GENE=TP53;STRAND=-;CDS=c.746G>T;AA=p.R249M;CNT=4 +17 7577536 COSM318150 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.745A>T;AA=p.R249W;CNT=3 +17 7577536 COSM363278 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.745A>G;AA=p.R249G;CNT=4 +17 7577536 COSM318149 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.745A>T;AA=p.R249W;CNT=3 +17 7577536 COSM363277 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.745A>G;AA=p.R249G;CNT=4 +17 7577536 COSM43629 T A . . GENE=TP53;STRAND=-;CDS=c.745A>T;AA=p.R249W;CNT=3 +17 7577536 COSM10668 T C . . GENE=TP53;STRAND=-;CDS=c.745A>G;AA=p.R249G;CNT=5 +17 7577538 COSM99021 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.464G>A;AA=p.R155Q;CNT=19 +17 7577538 COSM6549 C A . . GENE=TP53;STRAND=-;CDS=c.743G>T;AA=p.R248L;CNT=7 +17 7577538 COSM340106 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.743G>C;AA=p.R248P;CNT=4 +17 7577538 COSM241994 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.743G>T;AA=p.R248L;CNT=7 +17 7577538 COSM241995 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.743G>T;AA=p.R248L;CNT=7 +17 7577538 COSM11491 C G . . GENE=TP53;STRAND=-;CDS=c.743G>C;AA=p.R248P;CNT=4 +17 7577538 COSM340105 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.743G>C;AA=p.R248P;CNT=4 +17 7577538 COSM99602 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.743G>A;AA=p.R248Q;CNT=19 +17 7577538 COSM99020 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.743G>A;AA=p.R248Q;CNT=19 +17 7577538 COSM10662 C T . . GENE=TP53;STRAND=-;CDS=c.743G>A;AA=p.R248Q;CNT=31 +17 7577538 COSM241996 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.464G>T;AA=p.R155L;CNT=7 +17 7577538 COSM340107 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.464G>C;AA=p.R155P;CNT=4 +17 7577538 COSM6545 CGG CAA . . GENE=TP53;STRAND=-;CDS=c.741_742CC>TT;AA=p.R248W;CNT=3 +17 7577538 COSM112036 C CG . . GENE=TP53;STRAND=-;CDS=c.742_743insC;AA=p.R248fs*16;CNT=1 +17 7577538 COSM112039 C CG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.742_743insC;AA=p.R248fs*16;CNT=1 +17 7577538 COSM112038 C CG . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.463_464insC;AA=p.unknown;CNT=1 +17 7577538 COSM112037 C CG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.742_743insC;AA=p.R248fs*>39;CNT=1 +17 7577539 COSM120007 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.742C>T;AA=p.R248W;CNT=36 +17 7577539 COSM10656 G A . . GENE=TP53;STRAND=-;CDS=c.742C>T;AA=p.R248W;CNT=46 +17 7577539 COSM120005 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.742C>T;AA=p.R248W;CNT=36 +17 7577539 COSM1189381 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.742C>G;AA=p.R248G;CNT=1 +17 7577539 COSM1189383 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.463C>G;AA=p.R155G;CNT=1 +17 7577539 COSM1189382 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.742C>G;AA=p.R248G;CNT=1 +17 7577539 COSM11564 G C . . GENE=TP53;STRAND=-;CDS=c.742C>G;AA=p.R248G;CNT=2 +17 7577539 COSM120006 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.463C>T;AA=p.R155W;CNT=36 +17 7577541 COSM369278 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.740A>T;AA=p.N247I;CNT=2 +17 7577541 COSM43995 T A . . GENE=TP53;STRAND=-;CDS=c.740A>T;AA=p.N247I;CNT=2 +17 7577541 COSM369277 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.740A>T;AA=p.N247I;CNT=2 +17 7577541 COSM369279 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.461A>T;AA=p.N154I;CNT=2 +17 7577543 COSM10757 C G . . GENE=TP53;STRAND=-;CDS=c.738G>C;AA=p.M246I;CNT=1 +17 7577543 COSM1196423 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.738G>C;AA=p.M246I;CNT=1 +17 7577543 COSM1196424 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.459G>C;AA=p.M153I;CNT=1 +17 7577543 COSM1196422 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.738G>C;AA=p.M246I;CNT=1 +17 7577544 COSM213119 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.737T>C;AA=p.M246T;CNT=1 +17 7577544 COSM213121 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.458T>C;AA=p.M153T;CNT=1 +17 7577544 COSM213120 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.737T>C;AA=p.M246T;CNT=1 +17 7577544 COSM11355 A G . . GENE=TP53;STRAND=-;CDS=c.737T>C;AA=p.M246T;CNT=1 +17 7577544 COSM111715 ATGCCGC A . . GENE=TP53;STRAND=-;CDS=c.731_736delGCGGCA;AA=p.G244_M246>V;CNT=1 +17 7577544 COSM111718 ATGCCGC A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.731_736delGCGGCA;AA=p.G244_M246>V;CNT=1 +17 7577544 COSM111716 ATGCCGC A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.731_736delGCGGCA;AA=p.G244_M246>V;CNT=1 +17 7577544 COSM111717 ATGCCGC A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.452_457delGCGGCA;AA=p.G151_M153>V;CNT=1 +17 7577547 COSM179806 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.734G>A;AA=p.G245D;CNT=5 +17 7577547 COSM131475 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.734G>T;AA=p.G245V;CNT=5 +17 7577547 COSM179807 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.455G>A;AA=p.G152D;CNT=5 +17 7577547 COSM11196 C A . . GENE=TP53;STRAND=-;CDS=c.734G>T;AA=p.G245V;CNT=7 +17 7577547 COSM43606 C T . . GENE=TP53;STRAND=-;CDS=c.734G>A;AA=p.G245D;CNT=7 +17 7577547 COSM179805 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.734G>A;AA=p.G245D;CNT=5 +17 7577547 COSM131477 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.455G>T;AA=p.G152V;CNT=5 +17 7577547 COSM131476 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.734G>T;AA=p.G245V;CNT=5 +17 7577548 COSM562651 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.733G>T;AA=p.G245C;CNT=5 +17 7577548 COSM11081 C A . . GENE=TP53;STRAND=-;CDS=c.733G>T;AA=p.G245C;CNT=6 +17 7577548 COSM562652 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.733G>T;AA=p.G245C;CNT=5 +17 7577548 COSM121035 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.733G>A;AA=p.G245S;CNT=12 +17 7577548 COSM10957 C G . . GENE=TP53;STRAND=-;CDS=c.733G>C;AA=p.G245R;CNT=1 +17 7577548 COSM121037 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.454G>A;AA=p.G152S;CNT=12 +17 7577548 COSM121036 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.733G>A;AA=p.G245S;CNT=12 +17 7577548 COSM6932 C T . . GENE=TP53;STRAND=-;CDS=c.733G>A;AA=p.G245S;CNT=15 +17 7577548 COSM562653 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.454G>T;AA=p.G152C;CNT=5 +17 7577550 COSM179810 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.452G>A;AA=p.G151D;CNT=3 +17 7577550 COSM179808 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.731G>A;AA=p.G244D;CNT=3 +17 7577550 COSM10883 C T . . GENE=TP53;STRAND=-;CDS=c.731G>A;AA=p.G244D;CNT=4 +17 7577550 COSM179809 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.731G>A;AA=p.G244D;CNT=3 +17 7577551 COSM673604 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.451G>C;AA=p.G151R;CNT=1 +17 7577551 COSM673602 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.730G>C;AA=p.G244R;CNT=1 +17 7577551 COSM11524 C A . . GENE=TP53;STRAND=-;CDS=c.730G>T;AA=p.G244C;CNT=5 +17 7577551 COSM99683 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.730G>T;AA=p.G244C;CNT=3 +17 7577551 COSM10941 C T . . GENE=TP53;STRAND=-;CDS=c.730G>A;AA=p.G244S;CNT=1 +17 7577551 COSM984901 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.451G>A;AA=p.G151S;CNT=1 +17 7577551 COSM673603 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.730G>C;AA=p.G244R;CNT=1 +17 7577551 COSM44221 C G . . GENE=TP53;STRAND=-;CDS=c.730G>C;AA=p.G244R;CNT=1 +17 7577551 COSM984898 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.730G>A;AA=p.G244S;CNT=1 +17 7577551 COSM99685 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.730G>T;AA=p.G244C;CNT=3 +17 7577551 COSM984900 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.730G>A;AA=p.G244S;CNT=1 +17 7577551 COSM99684 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.451G>T;AA=p.G151C;CNT=3 +17 7577555 COSM1196893 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.447C>G;AA=p.C149W;CNT=2 +17 7577555 COSM11356 G C . . GENE=TP53;STRAND=-;CDS=c.726C>G;AA=p.C242W;CNT=2 +17 7577555 COSM1196892 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.726C>G;AA=p.C242W;CNT=2 +17 7577555 COSM1196891 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.726C>G;AA=p.C242W;CNT=2 +17 7577556 COSM251396 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.725G>A;AA=p.C242Y;CNT=1 +17 7577556 COSM251398 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.446G>A;AA=p.C149Y;CNT=1 +17 7577556 COSM10810 C A . . GENE=TP53;STRAND=-;CDS=c.725G>T;AA=p.C242F;CNT=6 +17 7577556 COSM129835 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.725G>T;AA=p.C242F;CNT=6 +17 7577556 COSM251397 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.725G>A;AA=p.C242Y;CNT=1 +17 7577556 COSM129836 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.446G>T;AA=p.C149F;CNT=6 +17 7577556 COSM129834 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.725G>T;AA=p.C242F;CNT=6 +17 7577556 COSM10646 C T . . GENE=TP53;STRAND=-;CDS=c.725G>A;AA=p.C242Y;CNT=1 +17 7577556 COSM85578 CAGGAACTGTTAC C . . GENE=TP53;STRAND=-;CDS=c.713_724del12;AA=p.N239_C242del;CNT=1 +17 7577557 COSM44935 A T . . GENE=TP53;STRAND=-;CDS=c.724T>A;AA=p.C242S;CNT=1 +17 7577557 COSM342677 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.724T>A;AA=p.C242S;CNT=1 +17 7577557 COSM342678 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.724T>A;AA=p.C242S;CNT=1 +17 7577557 COSM342679 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.445T>A;AA=p.C149S;CNT=1 +17 7577559 COSM10812 G A . . GENE=TP53;STRAND=-;CDS=c.722C>T;AA=p.S241F;CNT=10 +17 7577559 COSM214170 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.722C>T;AA=p.S241F;CNT=5 +17 7577559 COSM437502 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.722C>G;AA=p.S241C;CNT=1 +17 7577559 COSM1230112 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.443C>A;AA=p.S148Y;CNT=1 +17 7577559 COSM1230110 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.722C>A;AA=p.S241Y;CNT=1 +17 7577559 COSM10935 G T . . GENE=TP53;STRAND=-;CDS=c.722C>A;AA=p.S241Y;CNT=2 +17 7577559 COSM10709 G C . . GENE=TP53;STRAND=-;CDS=c.722C>G;AA=p.S241C;CNT=1 +17 7577559 COSM214171 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.722C>T;AA=p.S241F;CNT=5 +17 7577559 COSM1230111 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.722C>A;AA=p.S241Y;CNT=1 +17 7577559 COSM437503 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.443C>G;AA=p.S148C;CNT=1 +17 7577559 COSM437501 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.722C>G;AA=p.S241C;CNT=1 +17 7577559 COSM214172 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.443C>T;AA=p.S148F;CNT=5 +17 7577562 COSM111370 CTGTTACACA C . . GENE=TP53;STRAND=-;CDS=c.710_718delTGTGTAACA;AA=p.M237_N239delMCN;CNT=1 +17 7577562 COSM111373 CTGTTACACA C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.710_718delTGTGTAACA;AA=p.M237_N239delMCN;CNT=1 +17 7577562 COSM111371 CTGTTACACA C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.710_718delTGTGTAACA;AA=p.M237_N239delMCN;CNT=1 +17 7577562 COSM111372 CTGTTACACA C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.431_439delTGTGTAACA;AA=p.M144_N146delMCN;CNT=1 +17 7577564 COSM308202 G GT . . GENE=TP53;STRAND=-;CDS=c.716_717insA;AA=p.N239fs*25;CNT=1 +17 7577564 COSM308205 G GT . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.437_438insA;AA=p.N146fs*>10;CNT=1 +17 7577564 COSM308203 G GT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.716_717insA;AA=p.N239fs*>48;CNT=1 +17 7577564 COSM308204 G GT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.716_717insA;AA=p.N239fs*25;CNT=1 +17 7577565 COSM44094 T C . . GENE=TP53;STRAND=-;CDS=c.716A>G;AA=p.N239S;CNT=4 +17 7577565 COSM473433 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.716A>G;AA=p.N239S;CNT=3 +17 7577565 COSM473432 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.716A>G;AA=p.N239S;CNT=3 +17 7577565 COSM473434 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.437A>G;AA=p.N146S;CNT=3 +17 7577566 COSM984914 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.715A>G;AA=p.N239D;CNT=1 +17 7577566 COSM984917 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.436A>G;AA=p.N146D;CNT=1 +17 7577566 COSM10777 T C . . GENE=TP53;STRAND=-;CDS=c.715A>G;AA=p.N239D;CNT=1 +17 7577566 COSM984916 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.715A>G;AA=p.N239D;CNT=1 +17 7577566 COSM69195 T TA . . GENE=TP53;STRAND=-;CDS=c.714_715insT;AA=p.N239fs*1;CNT=2 +17 7577566 COSM112005 T TA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.714_715insT;AA=p.N239fs*1;CNT=1 +17 7577566 COSM112003 T TA . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.714_715insT;AA=p.N239fs*1;CNT=1 +17 7577566 COSM112004 T TA . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.435_436insT;AA=p.N146fs*1;CNT=1 +17 7577567 COSM1179295 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.714T>G;AA=p.C238W;CNT=1 +17 7577567 COSM44676 A C . . GENE=TP53;STRAND=-;CDS=c.714T>G;AA=p.C238W;CNT=1 +17 7577567 COSM1179297 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.435T>G;AA=p.C145W;CNT=1 +17 7577567 COSM1179296 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.714T>G;AA=p.C238W;CNT=1 +17 7577568 COSM99625 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.434G>T;AA=p.C145F;CNT=4 +17 7577568 COSM44653 C G . . GENE=TP53;STRAND=-;CDS=c.713G>C;AA=p.C238S;CNT=1 +17 7577568 COSM179812 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.713G>A;AA=p.C238Y;CNT=5 +17 7577568 COSM43778 C A . . GENE=TP53;STRAND=-;CDS=c.713G>T;AA=p.C238F;CNT=4 +17 7577568 COSM179811 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.713G>A;AA=p.C238Y;CNT=5 +17 7577568 COSM99626 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.713G>T;AA=p.C238F;CNT=4 +17 7577568 COSM99624 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.713G>T;AA=p.C238F;CNT=4 +17 7577568 COSM11059 C T . . GENE=TP53;STRAND=-;CDS=c.713G>A;AA=p.C238Y;CNT=6 +17 7577568 COSM249081 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.434G>C;AA=p.C145S;CNT=1 +17 7577568 COSM249080 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.713G>C;AA=p.C238S;CNT=1 +17 7577568 COSM179813 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.434G>A;AA=p.C145Y;CNT=5 +17 7577568 COSM249079 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.713G>C;AA=p.C238S;CNT=1 +17 7577570 COSM99647 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.432G>A;AA=p.M144I;CNT=2 +17 7577570 COSM1189385 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.711G>C;AA=p.M237I;CNT=1 +17 7577570 COSM1189384 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.711G>C;AA=p.M237I;CNT=1 +17 7577570 COSM301403 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.711G>T;AA=p.M237I;CNT=2 +17 7577570 COSM301404 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.432G>T;AA=p.M144I;CNT=2 +17 7577570 COSM44415 C G . . GENE=TP53;STRAND=-;CDS=c.711G>C;AA=p.M237I;CNT=1 +17 7577570 COSM99646 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.711G>A;AA=p.M237I;CNT=2 +17 7577570 COSM99648 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.711G>A;AA=p.M237I;CNT=2 +17 7577570 COSM301402 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.711G>T;AA=p.M237I;CNT=2 +17 7577570 COSM10834 C T . . GENE=TP53;STRAND=-;CDS=c.711G>A;AA=p.M237I;CNT=3 +17 7577570 COSM1189386 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.432G>C;AA=p.M144I;CNT=1 +17 7577570 COSM11063 C A . . GENE=TP53;STRAND=-;CDS=c.711G>T;AA=p.M237I;CNT=3 +17 7577571 COSM984920 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.710T>A;AA=p.M237K;CNT=1 +17 7577571 COSM984923 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.431T>A;AA=p.M144K;CNT=1 +17 7577571 COSM984922 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.710T>A;AA=p.M237K;CNT=1 +17 7577571 COSM43952 A T . . GENE=TP53;STRAND=-;CDS=c.710T>A;AA=p.M237K;CNT=2 +17 7577572 COSM220793 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.709A>T;AA=p.M237L;CNT=1 +17 7577572 COSM44965 T A . . GENE=TP53;STRAND=-;CDS=c.709A>T;AA=p.M237L;CNT=1 +17 7577572 COSM220794 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.430A>T;AA=p.M144L;CNT=1 +17 7577572 COSM220792 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.709A>T;AA=p.M237L;CNT=1 +17 7577573 COSM179814 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.708C>G;AA=p.Y236*;CNT=1 +17 7577573 COSM179816 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.429C>G;AA=p.Y143*;CNT=1 +17 7577573 COSM179815 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.708C>G;AA=p.Y236*;CNT=1 +17 7577573 COSM44960 G C . . GENE=TP53;STRAND=-;CDS=c.708C>G;AA=p.Y236*;CNT=1 +17 7577574 COSM116674 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.707A>G;AA=p.Y236C;CNT=5 +17 7577574 COSM10731 T C . . GENE=TP53;STRAND=-;CDS=c.707A>G;AA=p.Y236C;CNT=6 +17 7577574 COSM116673 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.428A>G;AA=p.Y143C;CNT=6 +17 7577574 COSM116672 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.707A>G;AA=p.Y236C;CNT=5 +17 7577575 COSM43826 A T . . GENE=TP53;STRAND=-;CDS=c.706T>A;AA=p.Y236N;CNT=1 +17 7577575 COSM1157852 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.706T>A;AA=p.Y236N;CNT=1 +17 7577575 COSM43602 A C . . GENE=TP53;STRAND=-;CDS=c.706T>G;AA=p.Y236D;CNT=1 +17 7577575 COSM129839 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.427T>G;AA=p.Y143D;CNT=1 +17 7577575 COSM129838 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.706T>G;AA=p.Y236D;CNT=1 +17 7577575 COSM1157851 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.706T>A;AA=p.Y236N;CNT=1 +17 7577575 COSM1157853 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.427T>A;AA=p.Y143N;CNT=1 +17 7577575 COSM129837 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.706T>G;AA=p.Y236D;CNT=1 +17 7577580 COSM99955 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.701A>C;AA=p.Y234S;CNT=2 +17 7577580 COSM165072 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.701A>G;AA=p.Y234C;CNT=7 +17 7577580 COSM165073 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.701A>G;AA=p.Y234C;CNT=7 +17 7577580 COSM99953 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.701A>C;AA=p.Y234S;CNT=2 +17 7577580 COSM99954 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.422A>C;AA=p.Y141S;CNT=2 +17 7577580 COSM43865 T G . . GENE=TP53;STRAND=-;CDS=c.701A>C;AA=p.Y234S;CNT=2 +17 7577580 COSM165074 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.422A>G;AA=p.Y141C;CNT=7 +17 7577580 COSM10725 T C . . GENE=TP53;STRAND=-;CDS=c.701A>G;AA=p.Y234C;CNT=9 +17 7577581 COSM146343 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.700T>G;AA=p.Y234D;CNT=1 +17 7577581 COSM11152 A G . . GENE=TP53;STRAND=-;CDS=c.700T>C;AA=p.Y234H;CNT=4 +17 7577581 COSM238605 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.700T>C;AA=p.Y234H;CNT=4 +17 7577581 COSM220768 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.700T>A;AA=p.Y234N;CNT=1 +17 7577581 COSM220767 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.700T>A;AA=p.Y234N;CNT=1 +17 7577581 COSM146344 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.421T>G;AA=p.Y141D;CNT=1 +17 7577581 COSM220769 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.421T>A;AA=p.Y141N;CNT=1 +17 7577581 COSM146342 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.700T>G;AA=p.Y234D;CNT=1 +17 7577581 COSM43956 A T . . GENE=TP53;STRAND=-;CDS=c.700T>A;AA=p.Y234N;CNT=2 +17 7577581 COSM43768 A C . . GENE=TP53;STRAND=-;CDS=c.700T>G;AA=p.Y234D;CNT=1 +17 7577581 COSM238606 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.421T>C;AA=p.Y141H;CNT=4 +17 7577581 COSM238604 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.700T>C;AA=p.Y234H;CNT=4 +17 7577584 COSM69170 GGATGGTGGTACA G . . GENE=TP53;STRAND=-;CDS=c.685_696del12;AA=p.C229_I232delCTTI;CNT=1 +17 7577585 COSM166246 G GCCA . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.695_696insTGG;AA=p.I232_H233insG;CNT=1 +17 7577585 COSM166245 G GCCA . . GENE=TP53;STRAND=-;CDS=c.695_696insTGG;AA=p.I232_H233insG;CNT=1 +17 7577585 COSM166247 G GCCA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.695_696insTGG;AA=p.I232_H233insG;CNT=1 +17 7577585 COSM166248 G GCCA . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.416_417insTGG;AA=p.I139_H140insG;CNT=1 +17 7577586 COSM984924 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.695T>C;AA=p.I232T;CNT=2 +17 7577586 COSM984927 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.416T>C;AA=p.I139T;CNT=2 +17 7577586 COSM984926 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.695T>C;AA=p.I232T;CNT=2 +17 7577586 COSM10715 A T . . GENE=TP53;STRAND=-;CDS=c.695T>A;AA=p.I232N;CNT=1 +17 7577586 COSM44601 A G . . GENE=TP53;STRAND=-;CDS=c.695T>C;AA=p.I232T;CNT=2 +17 7577587 COSM43550 T A . . GENE=TP53;STRAND=-;CDS=c.694A>T;AA=p.I232F;CNT=2 +17 7577587 COSM562649 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.694A>T;AA=p.I232F;CNT=2 +17 7577587 COSM562648 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.694A>T;AA=p.I232F;CNT=2 +17 7577587 COSM562650 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.415A>T;AA=p.I139F;CNT=2 +17 7577588 COSM44113 G A . . GENE=TP53;STRAND=-;CDS=c.693C>T;AA=p.T231T;CNT=1 +17 7577588 COSM287983 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.414C>T;AA=p.T138T;CNT=1 +17 7577588 COSM287982 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.693C>T;AA=p.T231T;CNT=1 +17 7577588 COSM287981 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.693C>T;AA=p.T231T;CNT=1 +17 7577590 COSM1193070 TGGT T . . GENE=TP53;STRAND=-;CDS=c.688_690delACC;AA=p.T231delT;CNT=1 +17 7577590 COSM1193071 TGGT T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.688_690delACC;AA=p.T231delT;CNT=1 +17 7577590 COSM1193072 TGGT T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.688_690delACC;AA=p.T231delT;CNT=1 +17 7577590 COSM1193073 TGGT T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.409_411delACC;AA=p.T138delT;CNT=1 +17 7577593 COSM44360 TAC T . . GENE=TP53;STRAND=-;CDS=c.686_687delGT;AA=p.C229fs*10;CNT=1 +17 7577593 COSM111637 TAC T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.686_687delGT;AA=p.C229fs*10;CNT=1 +17 7577593 COSM111635 TAC T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.686_687delGT;AA=p.C229fs*10;CNT=1 +17 7577593 COSM111636 TAC T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.407_408delGT;AA=p.C136fs*10;CNT=1 +17 7577595 COSM308323 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.686G>T;AA=p.C229F;CNT=1 +17 7577595 COSM308324 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.686G>T;AA=p.C229F;CNT=1 +17 7577595 COSM308325 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.407G>T;AA=p.C136F;CNT=1 +17 7577595 COSM308322 C A . . GENE=TP53;STRAND=-;CDS=c.686G>T;AA=p.C229F;CNT=1 +17 7577595 COSM308337 C CT . . GENE=TP53;STRAND=-;CDS=c.685_686insA;AA=p.C229fs*1;CNT=1 +17 7577595 COSM308339 C CT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.685_686insA;AA=p.C229fs*1;CNT=1 +17 7577595 COSM308340 C CT . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.406_407insA;AA=p.C136fs*1;CNT=1 +17 7577595 COSM308338 C CT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.685_686insA;AA=p.C229fs*1;CNT=1 +17 7577599 COSM69213 C CA . . GENE=TP53;STRAND=-;CDS=c.681_682insT;AA=p.D228fs*1;CNT=1 +17 7577603 COSM392089 GCCAACCTAGGAGATAACACAGGC G . . GENE=TP53;STRAND=-;CDS=c.673-18_677del23;AA=p.?;CNT=1 +17 7577603 COSM392090 GCCAACCTAGGAGATAACACAGGC G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.673-18_677del23;AA=p.?;CNT=1 +17 7577603 COSM392091 GCCAACCTAGGAGATAACACAGGC G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.673-18_677del23;AA=p.?;CNT=1 +17 7577603 COSM392092 GCCAACCTAGGAGATAACACAGGC G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.394-18_398del23;AA=p.?;CNT=1 +17 7577604 COSM674003 CC C . . GENE=TP53;STRAND=-;CDS=c.676delG;AA=p.G226fs*21;CNT=1 +17 7577604 COSM674005 CC C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.676delG;AA=p.G226fs*21;CNT=1 +17 7577604 COSM674004 CC C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.676delG;AA=p.G226fs*21;CNT=1 +17 7577604 COSM674006 CC C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.397delG;AA=p.G133fs*21;CNT=1 +17 7577609 COSM45135 C A . . GENE=TP53;STRAND=-;CDS=c.673-1G>T;AA=p.?;CNT=2 +17 7577609 COSM562646 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.673-1G>C;AA=p.?;CNT=1 +17 7577609 COSM562645 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.673-1G>C;AA=p.?;CNT=1 +17 7577609 COSM45675 C G . . GENE=TP53;STRAND=-;CDS=c.673-1G>C;AA=p.?;CNT=1 +17 7577609 COSM344604 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.673-1G>T;AA=p.?;CNT=2 +17 7577609 COSM562647 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.394-1G>C;AA=p.?;CNT=1 +17 7577609 COSM344605 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.394-1G>T;AA=p.?;CNT=2 +17 7577609 COSM43751 C T . . GENE=TP53;STRAND=-;CDS=c.673-1G>A;AA=p.?;CNT=1 +17 7577609 COSM344603 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.673-1G>T;AA=p.?;CNT=2 +17 7577610 COSM118999 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.673-2A>G;AA=p.?;CNT=2 +17 7577610 COSM323937 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.673-2A>T;AA=p.?;CNT=1 +17 7577610 COSM6908 T C . . GENE=TP53;STRAND=-;CDS=c.673-2A>G;AA=p.?;CNT=1 +17 7577610 COSM323939 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.394-2A>T;AA=p.?;CNT=1 +17 7577610 COSM323938 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.673-2A>T;AA=p.?;CNT=1 +17 7577610 COSM12559 T A . . GENE=TP53;STRAND=-;CDS=c.673-2A>T;AA=p.?;CNT=6 +17 7577610 COSM25225 T C . . GENE=TP53;STRAND=-;CDS=c.673-2A>G;AA=p.?;CNT=1 +17 7577610 COSM119000 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.394-2A>G;AA=p.?;CNT=2 +17 7577610 COSM119001 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.673-2A>G;AA=p.?;CNT=2 +17 7577610 COSM41575 T A . . GENE=TP53;STRAND=-;CDS=c.673-2A>T;AA=p.?;CNT=2 +17 7578173 COSM673751 AGACCTCAGGCGGCTCATAGGGCACCACCA A . . GENE=TP53;STRAND=-;CDS=c.647_672+3del29;AA=p.?;CNT=1 +17 7578173 COSM673753 AGACCTCAGGCGGCTCATAGGGCACCACCA A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.647_672+3del29;AA=p.?;CNT=1 +17 7578173 COSM673752 AGACCTCAGGCGGCTCATAGGGCACCACCA A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.647_672+3del29;AA=p.?;CNT=1 +17 7578173 COSM673754 AGACCTCAGGCGGCTCATAGGGCACCACCA A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.251_253-16del29;AA=p.?;CNT=1 +17 7578173 COSM673755 AGACCTCAGGCGGCTCATAGGGCACCACCA A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.368_393+3del29;AA=p.?;CNT=1 +17 7578175 COSM165067 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672+2T>A;AA=p.?;CNT=1 +17 7578175 COSM562642 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672+2T>C;AA=p.?;CNT=1 +17 7578175 COSM562644 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393+2T>C;AA=p.?;CNT=1 +17 7578175 COSM165069 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393+2T>A;AA=p.?;CNT=1 +17 7578175 COSM165066 A T . . GENE=TP53;STRAND=-;CDS=c.672+2T>A;AA=p.?;CNT=1 +17 7578175 COSM45517 A G . . GENE=TP53;STRAND=-;CDS=c.672+2T>C;AA=p.?;CNT=1 +17 7578175 COSM562643 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672+2T>C;AA=p.?;CNT=1 +17 7578175 COSM165068 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672+2T>A;AA=p.?;CNT=1 +17 7578176 COSM121038 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672+1G>C;AA=p.?;CNT=1 +17 7578176 COSM119012 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393+1G>A;AA=p.?;CNT=2 +17 7578176 COSM13586 C A . . GENE=TP53;STRAND=-;CDS=c.672+1G>T;AA=p.?;CNT=3 +17 7578176 COSM118940 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393+1G>T;AA=p.?;CNT=2 +17 7578176 COSM119011 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672+1G>A;AA=p.?;CNT=2 +17 7578176 COSM6906 C T . . GENE=TP53;STRAND=-;CDS=c.672+1G>A;AA=p.?;CNT=2 +17 7578176 COSM119013 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672+1G>A;AA=p.?;CNT=2 +17 7578176 COSM118939 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672+1G>T;AA=p.?;CNT=2 +17 7578176 COSM121039 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672+1G>C;AA=p.?;CNT=1 +17 7578176 COSM45367 C G . . GENE=TP53;STRAND=-;CDS=c.672+1G>C;AA=p.?;CNT=1 +17 7578176 COSM118941 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672+1G>T;AA=p.?;CNT=2 +17 7578176 COSM121040 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393+1G>C;AA=p.?;CNT=1 +17 7578177 COSM44754 C T . . GENE=TP53;STRAND=-;CDS=c.672G>A;AA=p.E224E;CNT=3 +17 7578177 COSM707900 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672G>C;AA=p.E224D;CNT=2 +17 7578177 COSM707901 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393G>C;AA=p.E131D;CNT=2 +17 7578177 COSM326731 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672G>T;AA=p.E224D;CNT=2 +17 7578177 COSM11451 C A . . GENE=TP53;STRAND=-;CDS=c.672G>T;AA=p.E224D;CNT=2 +17 7578177 COSM707896 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672G>A;AA=p.E224E;CNT=2 +17 7578177 COSM707897 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.672G>A;AA=p.E224E;CNT=2 +17 7578177 COSM44945 C G . . GENE=TP53;STRAND=-;CDS=c.672G>C;AA=p.E224D;CNT=2 +17 7578177 COSM326732 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672G>T;AA=p.E224D;CNT=2 +17 7578177 COSM707899 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.672G>C;AA=p.E224D;CNT=2 +17 7578177 COSM326733 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393G>T;AA=p.E131D;CNT=2 +17 7578177 COSM707898 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.393G>A;AA=p.E131E;CNT=2 +17 7578178 COSM69018 TCA T . . GENE=TP53;STRAND=-;CDS=c.669_670delTG;AA=p.E224fs*4;CNT=1 +17 7578181 COSM111639 GGC G . . GENE=TP53;STRAND=-;CDS=c.666_667delGC;AA=p.P223fs*1;CNT=1 +17 7578181 COSM111642 GGC G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.666_667delGC;AA=p.P223fs*1;CNT=1 +17 7578181 COSM111640 GGC G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.666_667delGC;AA=p.P223fs*1;CNT=1 +17 7578181 COSM111641 GGC G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.387_388delGC;AA=p.P130fs*1;CNT=1 +17 7578188 COSM126983 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.661G>T;AA=p.E221*;CNT=3 +17 7578188 COSM126982 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.661G>T;AA=p.E221*;CNT=3 +17 7578188 COSM126984 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.382G>T;AA=p.E128*;CNT=3 +17 7578188 COSM44817 C A . . GENE=TP53;STRAND=-;CDS=c.661G>T;AA=p.E221*;CNT=3 +17 7578190 COSM99718 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.659A>G;AA=p.Y220C;CNT=24 +17 7578190 COSM99719 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.380A>G;AA=p.Y127C;CNT=24 +17 7578190 COSM99720 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.659A>G;AA=p.Y220C;CNT=24 +17 7578190 COSM10758 T C . . GENE=TP53;STRAND=-;CDS=c.659A>G;AA=p.Y220C;CNT=30 +17 7578191 COSM1172476 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.658T>C;AA=p.Y220H;CNT=1 +17 7578191 COSM44637 A G . . GENE=TP53;STRAND=-;CDS=c.658T>C;AA=p.Y220H;CNT=1 +17 7578191 COSM1172479 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.252+10T>C;AA=p.?;CNT=1 +17 7578191 COSM1172477 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.658T>C;AA=p.Y220H;CNT=1 +17 7578191 COSM1172478 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.379T>C;AA=p.Y127H;CNT=1 +17 7578202 COSM119679 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.251T>G;AA=p.V84G;CNT=1 +17 7578202 COSM707895 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.251T>A;AA=p.V84E;CNT=1 +17 7578202 COSM119681 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.647T>G;AA=p.V216G;CNT=1 +17 7578202 COSM43681 A C . . GENE=TP53;STRAND=-;CDS=c.647T>G;AA=p.V216G;CNT=1 +17 7578202 COSM119680 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.368T>G;AA=p.V123G;CNT=1 +17 7578202 COSM707894 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.368T>A;AA=p.V123E;CNT=1 +17 7578202 COSM44274 A T . . GENE=TP53;STRAND=-;CDS=c.647T>A;AA=p.V216E;CNT=1 +17 7578202 COSM707892 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.647T>A;AA=p.V216E;CNT=1 +17 7578202 COSM119678 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.647T>G;AA=p.V216G;CNT=1 +17 7578202 COSM707893 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.647T>A;AA=p.V216E;CNT=1 +17 7578203 COSM120095 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.646G>A;AA=p.V216M;CNT=3 +17 7578203 COSM10667 C T . . GENE=TP53;STRAND=-;CDS=c.646G>A;AA=p.V216M;CNT=4 +17 7578203 COSM120098 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.646G>A;AA=p.V216M;CNT=3 +17 7578203 COSM120096 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.250G>A;AA=p.V84M;CNT=3 +17 7578203 COSM120097 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.367G>A;AA=p.V123M;CNT=3 +17 7578204 COSM220771 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.645T>G;AA=p.S215R;CNT=2 +17 7578204 COSM220773 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.366T>G;AA=p.S122R;CNT=2 +17 7578204 COSM45122 A T . . GENE=TP53;STRAND=-;CDS=c.645T>A;AA=p.S215R;CNT=1 +17 7578204 COSM44979 A C . . GENE=TP53;STRAND=-;CDS=c.645T>G;AA=p.S215R;CNT=3 +17 7578204 COSM220772 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.249T>G;AA=p.S83R;CNT=2 +17 7578204 COSM220770 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.645T>G;AA=p.S215R;CNT=2 +17 7578205 COSM326721 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.248G>T;AA=p.S83I;CNT=2 +17 7578205 COSM326720 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.644G>T;AA=p.S215I;CNT=2 +17 7578205 COSM326719 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.644G>T;AA=p.S215I;CNT=2 +17 7578205 COSM326722 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.365G>T;AA=p.S122I;CNT=2 +17 7578205 COSM11450 C A . . GENE=TP53;STRAND=-;CDS=c.644G>T;AA=p.S215I;CNT=2 +17 7578207 COSM128666 AT A . . GENE=TP53;STRAND=-;CDS=c.641delA;AA=p.H214fs*33;CNT=1 +17 7578207 COSM128667 AT A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.641delA;AA=p.H214fs*33;CNT=1 +17 7578207 COSM128668 AT A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.641delA;AA=p.H214fs*33;CNT=1 +17 7578207 COSM128670 AT A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.245delA;AA=p.H82fs*>9;CNT=1 +17 7578207 COSM128669 AT A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.362delA;AA=p.H121fs*33;CNT=1 +17 7578208 COSM307279 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.641A>G;AA=p.H214R;CNT=5 +17 7578208 COSM307281 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.245A>G;AA=p.H82R;CNT=5 +17 7578208 COSM43687 T C . . GENE=TP53;STRAND=-;CDS=c.641A>G;AA=p.H214R;CNT=6 +17 7578208 COSM307282 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.362A>G;AA=p.H121R;CNT=5 +17 7578208 COSM307280 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.641A>G;AA=p.H214R;CNT=5 +17 7578211 COSM131467 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.638G>A;AA=p.R213Q;CNT=2 +17 7578211 COSM131469 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.242G>A;AA=p.R81Q;CNT=2 +17 7578211 COSM10735 C T . . GENE=TP53;STRAND=-;CDS=c.638G>A;AA=p.R213Q;CNT=2 +17 7578211 COSM241999 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.242G>T;AA=p.R81L;CNT=3 +17 7578211 COSM242000 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.359G>T;AA=p.R120L;CNT=3 +17 7578211 COSM241998 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.638G>T;AA=p.R213L;CNT=3 +17 7578211 COSM43650 C A . . GENE=TP53;STRAND=-;CDS=c.638G>T;AA=p.R213L;CNT=3 +17 7578211 COSM131466 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.638G>A;AA=p.R213Q;CNT=2 +17 7578211 COSM241997 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.638G>T;AA=p.R213L;CNT=3 +17 7578211 COSM131468 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.359G>A;AA=p.R120Q;CNT=2 +17 7578212 COSM707891 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.241C>G;AA=p.R81G;CNT=1 +17 7578212 COSM99616 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.241C>T;AA=p.R81*;CNT=27 +17 7578212 COSM707889 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.637C>G;AA=p.R213G;CNT=1 +17 7578212 COSM707888 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.637C>G;AA=p.R213G;CNT=1 +17 7578212 COSM99615 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.637C>T;AA=p.R213*;CNT=27 +17 7578212 COSM44102 G C . . GENE=TP53;STRAND=-;CDS=c.637C>G;AA=p.R213G;CNT=1 +17 7578212 COSM99617 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.358C>T;AA=p.R120*;CNT=27 +17 7578212 COSM10654 G A . . GENE=TP53;STRAND=-;CDS=c.637C>T;AA=p.R213*;CNT=28 +17 7578212 COSM99618 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.637C>T;AA=p.R213*;CNT=27 +17 7578212 COSM707890 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.358C>G;AA=p.R120G;CNT=1 +17 7578212 COSM128710 G GAA . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.636_637insTT;AA=p.R213fs*35;CNT=1 +17 7578212 COSM128713 G GAA . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.240_241insTT;AA=p.R81fs*>11;CNT=1 +17 7578212 COSM128709 G GAA . . GENE=TP53;STRAND=-;CDS=c.636_637insTT;AA=p.R213fs*35;CNT=1 +17 7578212 COSM128711 G GAA . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.636_637insTT;AA=p.R213fs*35;CNT=1 +17 7578212 COSM128712 G GAA . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.357_358insTT;AA=p.R120fs*35;CNT=1 +17 7578212 COSM44162 GAA G . . GENE=TP53;STRAND=-;CDS=c.635_636delTT;AA=p.F212fs*3;CNT=1 +17 7578212 COSM292496 GAA G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.635_636delTT;AA=p.F212fs*3;CNT=1 +17 7578212 COSM292495 GAA G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.635_636delTT;AA=p.F212fs*3;CNT=1 +17 7578212 COSM292497 GAA G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.239_240delTT;AA=p.F80fs*3;CNT=1 +17 7578212 COSM292498 GAA G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.356_357delTT;AA=p.F119fs*3;CNT=1 +17 7578219 COSM69086 GTTTCT G . . GENE=TP53;STRAND=-;CDS=c.625_629delAGAAA;AA=p.R209fs*5;CNT=1 +17 7578221 COSM13120 TTC T . . GENE=TP53;STRAND=-;CDS=c.626_627delGA;AA=p.R209fs*6;CNT=4 +17 7578221 COSM392316 TTC T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.626_627delGA;AA=p.R209fs*6;CNT=4 +17 7578221 COSM392317 TTC T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.626_627delGA;AA=p.R209fs*6;CNT=4 +17 7578221 COSM392319 TTC T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.230_231delGA;AA=p.R77fs*6;CNT=4 +17 7578221 COSM392318 TTC T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.347_348delGA;AA=p.R116fs*6;CNT=4 +17 7578222 COSM6482 TCT T . . GENE=TP53;STRAND=-;CDS=c.625_626delAG;AA=p.R209fs*6;CNT=1 +17 7578222 COSM242002 TCT T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.625_626delAG;AA=p.R209fs*6;CNT=1 +17 7578222 COSM242001 TCT T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.625_626delAG;AA=p.R209fs*6;CNT=1 +17 7578222 COSM242003 TCT T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.229_230delAG;AA=p.R77fs*6;CNT=1 +17 7578222 COSM242004 TCT T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.346_347delAG;AA=p.R116fs*6;CNT=1 +17 7578224 COSM11290 T A . . GENE=TP53;STRAND=-;CDS=c.625A>T;AA=p.R209*;CNT=2 +17 7578224 COSM323942 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.625A>T;AA=p.R209*;CNT=2 +17 7578224 COSM323943 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.625A>T;AA=p.R209*;CNT=2 +17 7578224 COSM323945 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.346A>T;AA=p.R116*;CNT=2 +17 7578224 COSM323944 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.229A>T;AA=p.R77*;CNT=2 +17 7578226 COSM44249 T A . . GENE=TP53;STRAND=-;CDS=c.623A>T;AA=p.D208V;CNT=1 +17 7578230 COSM179817 C T . . GENE=TP53;STRAND=-;CDS=c.619G>A;AA=p.D207N;CNT=1 +17 7578230 COSM179821 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.340G>A;AA=p.D114N;CNT=1 +17 7578230 COSM179820 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.223G>A;AA=p.D75N;CNT=1 +17 7578230 COSM179819 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.619G>A;AA=p.D207N;CNT=1 +17 7578230 COSM179818 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.619G>A;AA=p.D207N;CNT=1 +17 7578235 COSM99630 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.614A>G;AA=p.Y205C;CNT=6 +17 7578235 COSM99632 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.335A>G;AA=p.Y112C;CNT=6 +17 7578235 COSM215720 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.614A>C;AA=p.Y205S;CNT=1 +17 7578235 COSM215721 T G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.218A>C;AA=p.Y73S;CNT=1 +17 7578235 COSM44169 T G . . GENE=TP53;STRAND=-;CDS=c.614A>C;AA=p.Y205S;CNT=1 +17 7578235 COSM99633 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.614A>G;AA=p.Y205C;CNT=6 +17 7578235 COSM215722 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.335A>C;AA=p.Y112S;CNT=1 +17 7578235 COSM215719 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.614A>C;AA=p.Y205S;CNT=1 +17 7578235 COSM43947 T C . . GENE=TP53;STRAND=-;CDS=c.614A>G;AA=p.Y205C;CNT=8 +17 7578235 COSM99631 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.218A>G;AA=p.Y73C;CNT=6 +17 7578236 COSM220763 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.217T>A;AA=p.Y73N;CNT=2 +17 7578236 COSM1159832 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.334T>C;AA=p.Y112H;CNT=1 +17 7578236 COSM220764 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.334T>A;AA=p.Y112N;CNT=2 +17 7578236 COSM1159830 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.613T>C;AA=p.Y205H;CNT=1 +17 7578236 COSM220761 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.613T>A;AA=p.Y205N;CNT=2 +17 7578236 COSM1159833 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.217T>C;AA=p.Y73H;CNT=1 +17 7578236 COSM220762 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.613T>A;AA=p.Y205N;CNT=2 +17 7578236 COSM1159831 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.613T>C;AA=p.Y205H;CNT=1 +17 7578236 COSM45685 A T . . GENE=TP53;STRAND=-;CDS=c.613T>A;AA=p.Y205N;CNT=2 +17 7578236 COSM43642 A G . . GENE=TP53;STRAND=-;CDS=c.613T>C;AA=p.Y205H;CNT=1 +17 7578237 COSM984941 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.333G>C;AA=p.E111D;CNT=1 +17 7578237 COSM984942 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.216G>C;AA=p.E72D;CNT=1 +17 7578237 COSM984940 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.612G>C;AA=p.E204D;CNT=1 +17 7578237 COSM46471 C G . . GENE=TP53;STRAND=-;CDS=c.612G>C;AA=p.E204D;CNT=1 +17 7578237 COSM984938 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.612G>C;AA=p.E204D;CNT=1 +17 7578239 COSM10804 C A . . GENE=TP53;STRAND=-;CDS=c.610G>T;AA=p.E204*;CNT=5 +17 7578239 COSM165086 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.610G>T;AA=p.E204*;CNT=3 +17 7578239 COSM165089 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.331G>T;AA=p.E111*;CNT=3 +17 7578239 COSM165087 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.610G>T;AA=p.E204*;CNT=3 +17 7578239 COSM165088 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.214G>T;AA=p.E72*;CNT=3 +17 7578247 COSM85577 AAATTTCCTT A . . GENE=TP53;STRAND=-;CDS=c.593_601delAAGGAAATT;AA=p.E198_L201>V;CNT=1 +17 7578253 COSM44140 C A . . GENE=TP53;STRAND=-;CDS=c.596G>T;AA=p.G199V;CNT=3 +17 7578253 COSM255790 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.317G>T;AA=p.G106V;CNT=2 +17 7578253 COSM255789 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.200G>T;AA=p.G67V;CNT=2 +17 7578253 COSM255787 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.596G>T;AA=p.G199V;CNT=2 +17 7578253 COSM255788 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.596G>T;AA=p.G199V;CNT=2 +17 7578254 COSM44537 C A . . GENE=TP53;STRAND=-;CDS=c.595G>T;AA=p.G199*;CNT=1 +17 7578254 COSM378224 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.595G>T;AA=p.G199*;CNT=1 +17 7578254 COSM378227 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.199G>T;AA=p.G67*;CNT=1 +17 7578254 COSM378225 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.595G>T;AA=p.G199*;CNT=1 +17 7578254 COSM378226 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.316G>T;AA=p.G106*;CNT=1 +17 7578256 COSM44702 TC T . . GENE=TP53;STRAND=-;CDS=c.592delG;AA=p.E198fs*49;CNT=1 +17 7578256 COSM166240 TCCACTCGGATAAGATGCTGAG T . . GENE=TP53;STRAND=-;CDS=c.572_592del21;AA=p.P191_E198>Q;CNT=1 +17 7578256 COSM391541 TC T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.592delG;AA=p.E198fs*49;CNT=1 +17 7578256 COSM166242 TCCACTCGGATAAGATGCTGAG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.572_592del21;AA=p.P191_E198>Q;CNT=1 +17 7578256 COSM391542 TC T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.592delG;AA=p.E198fs*49;CNT=1 +17 7578256 COSM166241 TCCACTCGGATAAGATGCTGAG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.572_592del21;AA=p.P191_E198>Q;CNT=1 +17 7578256 COSM391544 TC T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.196delG;AA=p.E66fs*>25;CNT=1 +17 7578256 COSM166243 TCCACTCGGATAAGATGCTGAG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.176_196del21;AA=p.P59_E66>Q;CNT=1 +17 7578256 COSM391543 TC T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.313delG;AA=p.E105fs*49;CNT=1 +17 7578256 COSM166244 TCCACTCGGATAAGATGCTGAG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.293_313del21;AA=p.P98_E105>Q;CNT=1 +17 7578257 COSM118012 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.313G>T;AA=p.E105*;CNT=2 +17 7578257 COSM118010 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.592G>T;AA=p.E198*;CNT=2 +17 7578257 COSM118013 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.592G>T;AA=p.E198*;CNT=2 +17 7578257 COSM118011 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.196G>T;AA=p.E66*;CNT=2 +17 7578257 COSM44241 C A . . GENE=TP53;STRAND=-;CDS=c.592G>T;AA=p.E198*;CNT=3 +17 7578260 COSM307273 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.193G>T;AA=p.V65L;CNT=1 +17 7578260 COSM307274 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.310G>T;AA=p.V104L;CNT=1 +17 7578260 COSM307272 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.589G>T;AA=p.V197L;CNT=1 +17 7578260 COSM46212 C A . . GENE=TP53;STRAND=-;CDS=c.589G>T;AA=p.V197L;CNT=1 +17 7578260 COSM307271 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.589G>T;AA=p.V197L;CNT=1 +17 7578261 COSM1180844 TCG T . . GENE=TP53;STRAND=-;CDS=c.586_587delCG;AA=p.R196fs*12;CNT=2 +17 7578261 COSM1180845 TCG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.586_587delCG;AA=p.R196fs*12;CNT=2 +17 7578261 COSM1180846 TCG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.586_587delCG;AA=p.R196fs*12;CNT=2 +17 7578261 COSM1180848 TCG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.190_191delCG;AA=p.R64fs*12;CNT=2 +17 7578261 COSM1180847 TCG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.307_308delCG;AA=p.R103fs*12;CNT=2 +17 7578262 COSM218534 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.191G>C;AA=p.R64P;CNT=3 +17 7578262 COSM218535 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.308G>C;AA=p.R103P;CNT=3 +17 7578262 COSM218532 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.587G>C;AA=p.R196P;CNT=2 +17 7578262 COSM218533 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.587G>C;AA=p.R196P;CNT=2 +17 7578262 COSM43814 C G . . GENE=TP53;STRAND=-;CDS=c.587G>C;AA=p.R196P;CNT=2 +17 7578262 COSM44757 CG C . . GENE=TP53;STRAND=-;CDS=c.586delC;AA=p.R196fs*51;CNT=2 +17 7578262 COSM166215 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.586delC;AA=p.R196fs*51;CNT=2 +17 7578262 COSM166214 CG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.586delC;AA=p.R196fs*51;CNT=2 +17 7578262 COSM166216 CG C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.190delC;AA=p.R64fs*>27;CNT=2 +17 7578262 COSM166217 CG C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.307delC;AA=p.R103fs*51;CNT=2 +17 7578263 COSM99667 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.307C>T;AA=p.R103*;CNT=13 +17 7578263 COSM99668 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.586C>T;AA=p.R196*;CNT=13 +17 7578263 COSM99665 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.586C>T;AA=p.R196*;CNT=13 +17 7578263 COSM99666 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.190C>T;AA=p.R64*;CNT=13 +17 7578263 COSM10705 G A . . GENE=TP53;STRAND=-;CDS=c.586C>T;AA=p.R196*;CNT=16 +17 7578264 COSM562637 G C . . GENE=TP53;STRAND=-;CDS=c.585C>G;AA=p.I195M;CNT=1 +17 7578264 COSM562639 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.585C>G;AA=p.I195M;CNT=1 +17 7578264 COSM562641 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.189C>G;AA=p.I63M;CNT=1 +17 7578264 COSM562638 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.585C>G;AA=p.I195M;CNT=1 +17 7578264 COSM562640 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.306C>G;AA=p.I102M;CNT=1 +17 7578265 COSM11089 A G . . GENE=TP53;STRAND=-;CDS=c.584T>C;AA=p.I195T;CNT=9 +17 7578265 COSM116922 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.188T>C;AA=p.I63T;CNT=2 +17 7578265 COSM116924 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.584T>C;AA=p.I195T;CNT=2 +17 7578265 COSM44877 A T . . GENE=TP53;STRAND=-;CDS=c.584T>A;AA=p.I195N;CNT=1 +17 7578265 COSM116921 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.584T>C;AA=p.I195T;CNT=2 +17 7578265 COSM212745 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.584T>G;AA=p.I195S;CNT=2 +17 7578265 COSM212746 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.188T>G;AA=p.I63S;CNT=2 +17 7578265 COSM212747 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.305T>G;AA=p.I102S;CNT=2 +17 7578265 COSM44539 A C . . GENE=TP53;STRAND=-;CDS=c.584T>G;AA=p.I195S;CNT=2 +17 7578265 COSM212744 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.584T>G;AA=p.I195S;CNT=2 +17 7578265 COSM116923 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.305T>C;AA=p.I102T;CNT=2 +17 7578265 COSM295520 A AT . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.187_188insA;AA=p.I63fs*14;CNT=1 +17 7578265 COSM295521 A AT . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.304_305insA;AA=p.I102fs*14;CNT=1 +17 7578265 COSM295519 A AT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.583_584insA;AA=p.I195fs*14;CNT=1 +17 7578265 COSM295518 A AT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.583_584insA;AA=p.I195fs*14;CNT=1 +17 7578265 COSM295517 A AT . . GENE=TP53;STRAND=-;CDS=c.583_584insA;AA=p.I195fs*14;CNT=1 +17 7578265 COSM69179 ATAAGATGCTGAGGAGGGGCCAGACC A . . GENE=TP53;STRAND=-;CDS=c.560-1_583del25;AA=p.?;CNT=1 +17 7578266 COSM129840 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.583A>T;AA=p.I195F;CNT=1 +17 7578266 COSM44633 T A . . GENE=TP53;STRAND=-;CDS=c.583A>T;AA=p.I195F;CNT=2 +17 7578266 COSM129841 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.583A>T;AA=p.I195F;CNT=1 +17 7578266 COSM129843 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.187A>T;AA=p.I63F;CNT=1 +17 7578266 COSM129842 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.304A>T;AA=p.I102F;CNT=1 +17 7578268 COSM117650 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.581T>G;AA=p.L194R;CNT=4 +17 7578268 COSM43623 A T . . GENE=TP53;STRAND=-;CDS=c.581T>A;AA=p.L194H;CNT=1 +17 7578268 COSM169018 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.581T>A;AA=p.L194H;CNT=1 +17 7578268 COSM169019 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.581T>A;AA=p.L194H;CNT=1 +17 7578268 COSM169021 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.302T>A;AA=p.L101H;CNT=1 +17 7578268 COSM169020 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.185T>A;AA=p.L62H;CNT=1 +17 7578268 COSM117648 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.185T>G;AA=p.L62R;CNT=4 +17 7578268 COSM44571 A C . . GENE=TP53;STRAND=-;CDS=c.581T>G;AA=p.L194R;CNT=5 +17 7578268 COSM117649 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.302T>G;AA=p.L101R;CNT=4 +17 7578268 COSM117647 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.581T>G;AA=p.L194R;CNT=4 +17 7578269 COSM376383 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.301C>T;AA=p.L101F;CNT=1 +17 7578269 COSM376381 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.580C>T;AA=p.L194F;CNT=1 +17 7578269 COSM376384 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.184C>T;AA=p.L62F;CNT=1 +17 7578269 COSM10995 G A . . GENE=TP53;STRAND=-;CDS=c.580C>T;AA=p.L194F;CNT=1 +17 7578269 COSM376382 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.580C>T;AA=p.L194F;CNT=1 +17 7578271 COSM308308 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.182A>G;AA=p.H61R;CNT=2 +17 7578271 COSM99919 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.578A>T;AA=p.H193L;CNT=5 +17 7578271 COSM131460 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.299A>C;AA=p.H100P;CNT=1 +17 7578271 COSM43833 T G . . GENE=TP53;STRAND=-;CDS=c.578A>C;AA=p.H193P;CNT=1 +17 7578271 COSM99918 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.299A>T;AA=p.H100L;CNT=5 +17 7578271 COSM99916 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.578A>T;AA=p.H193L;CNT=5 +17 7578271 COSM131461 T G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.182A>C;AA=p.H61P;CNT=1 +17 7578271 COSM131459 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.578A>C;AA=p.H193P;CNT=1 +17 7578271 COSM308309 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.299A>G;AA=p.H100R;CNT=2 +17 7578271 COSM10742 T C . . GENE=TP53;STRAND=-;CDS=c.578A>G;AA=p.H193R;CNT=6 +17 7578271 COSM308307 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.578A>G;AA=p.H193R;CNT=2 +17 7578271 COSM11066 T A . . GENE=TP53;STRAND=-;CDS=c.578A>T;AA=p.H193L;CNT=5 +17 7578271 COSM99917 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.182A>T;AA=p.H61L;CNT=5 +17 7578271 COSM131458 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.578A>C;AA=p.H193P;CNT=1 +17 7578271 COSM308306 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.578A>G;AA=p.H193R;CNT=2 +17 7578272 COSM251419 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.298C>G;AA=p.H100D;CNT=1 +17 7578272 COSM44002 G C . . GENE=TP53;STRAND=-;CDS=c.577C>G;AA=p.H193D;CNT=1 +17 7578272 COSM437531 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.298C>T;AA=p.H100Y;CNT=6 +17 7578272 COSM437532 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.181C>T;AA=p.H61Y;CNT=6 +17 7578272 COSM10672 G A . . GENE=TP53;STRAND=-;CDS=c.577C>T;AA=p.H193Y;CNT=7 +17 7578272 COSM251416 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.577C>G;AA=p.H193D;CNT=1 +17 7578272 COSM251417 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.577C>G;AA=p.H193D;CNT=1 +17 7578272 COSM251418 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.181C>G;AA=p.H61D;CNT=1 +17 7578272 COSM437529 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.577C>T;AA=p.H193Y;CNT=6 +17 7578272 COSM437530 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.577C>T;AA=p.H193Y;CNT=6 +17 7578274 COSM45140 TGAG T . . GENE=TP53;STRAND=-;CDS=c.572_574delCTC;AA=p.P191delP;CNT=3 +17 7578274 COSM111724 TGAG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.572_574delCTC;AA=p.P191delP;CNT=2 +17 7578274 COSM111721 TGAG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.572_574delCTC;AA=p.P191delP;CNT=2 +17 7578274 COSM111722 TGAG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.176_178delCTC;AA=p.P59delP;CNT=2 +17 7578274 COSM111723 TGAG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.293_295delCTC;AA=p.P98delP;CNT=2 +17 7578275 COSM117948 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.295C>T;AA=p.Q99*;CNT=7 +17 7578275 COSM117949 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.574C>T;AA=p.Q192*;CNT=7 +17 7578275 COSM117946 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.574C>T;AA=p.Q192*;CNT=7 +17 7578275 COSM117947 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.178C>T;AA=p.Q60*;CNT=7 +17 7578275 COSM10733 G A . . GENE=TP53;STRAND=-;CDS=c.574C>T;AA=p.Q192*;CNT=8 +17 7578280 COSM1189389 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.290C>G;AA=p.P97R;CNT=1 +17 7578280 COSM44004 G C . . GENE=TP53;STRAND=-;CDS=c.569C>G;AA=p.P190R;CNT=1 +17 7578280 COSM1189387 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.569C>G;AA=p.P190R;CNT=1 +17 7578280 COSM1189390 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.173C>G;AA=p.P58R;CNT=1 +17 7578280 COSM1189388 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.569C>G;AA=p.P190R;CNT=1 +17 7578287 COSM391613 GAC G . . GENE=TP53;STRAND=-;CDS=c.560_561delGT;AA=p.G187fs*21;CNT=1 +17 7578287 COSM391614 GAC G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560_561delGT;AA=p.G187fs*21;CNT=1 +17 7578287 COSM391615 GAC G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560_561delGT;AA=p.G187fs*21;CNT=1 +17 7578287 COSM391617 GAC G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164_165delGT;AA=p.G55fs*21;CNT=1 +17 7578287 COSM391616 GAC G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281_282delGT;AA=p.G94fs*21;CNT=1 +17 7578290 COSM341765 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281-1G>C;AA=p.?;CNT=1 +17 7578290 COSM127201 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560-1G>A;AA=p.?;CNT=3 +17 7578290 COSM127200 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560-1G>A;AA=p.?;CNT=3 +17 7578290 COSM341766 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164-1G>C;AA=p.?;CNT=1 +17 7578290 COSM335066 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164-1G>T;AA=p.?;CNT=2 +17 7578290 COSM43872 C G . . GENE=TP53;STRAND=-;CDS=c.560-1G>C;AA=p.?;CNT=2 +17 7578290 COSM127203 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164-1G>A;AA=p.?;CNT=3 +17 7578290 COSM43753 C T . . GENE=TP53;STRAND=-;CDS=c.560-1G>A;AA=p.?;CNT=5 +17 7578290 COSM335065 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281-1G>T;AA=p.?;CNT=2 +17 7578290 COSM335063 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560-1G>T;AA=p.?;CNT=2 +17 7578290 COSM341764 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560-1G>C;AA=p.?;CNT=1 +17 7578290 COSM127202 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281-1G>A;AA=p.?;CNT=3 +17 7578290 COSM43841 C A . . GENE=TP53;STRAND=-;CDS=c.560-1G>T;AA=p.?;CNT=2 +17 7578290 COSM335064 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560-1G>T;AA=p.?;CNT=2 +17 7578290 COSM341763 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560-1G>C;AA=p.?;CNT=1 +17 7578291 COSM323928 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281-2A>C;AA=p.?;CNT=1 +17 7578291 COSM323925 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560-2A>C;AA=p.?;CNT=1 +17 7578291 COSM45031 T G . . GENE=TP53;STRAND=-;CDS=c.560-2A>C;AA=p.?;CNT=1 +17 7578291 COSM323927 T G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164-2A>C;AA=p.?;CNT=1 +17 7578291 COSM323926 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560-2A>C;AA=p.?;CNT=1 +17 7578292 COSM148177 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.560-3T>G;AA=p.?;CNT=1 +17 7578292 COSM148176 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.560-3T>G;AA=p.?;CNT=1 +17 7578292 COSM46059 A C . . GENE=TP53;STRAND=-;CDS=c.560-3T>G;AA=p.?;CNT=1 +17 7578292 COSM148179 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.281-3T>G;AA=p.?;CNT=1 +17 7578292 COSM148178 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.164-3T>G;AA=p.?;CNT=1 +17 7578369 COSM99923 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.559+2T>G;AA=p.?;CNT=1 +17 7578369 COSM99920 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.559+2T>G;AA=p.?;CNT=1 +17 7578369 COSM99922 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.280+2T>G;AA=p.?;CNT=1 +17 7578369 COSM45711 A C . . GENE=TP53;STRAND=-;CDS=c.559+2T>G;AA=p.?;CNT=2 +17 7578369 COSM99921 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.163+2T>G;AA=p.?;CNT=1 +17 7578370 COSM6901 C T . . GENE=TP53;STRAND=-;CDS=c.559+1G>A;AA=p.?;CNT=3 +17 7578370 COSM131535 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.559+1G>A;AA=p.?;CNT=2 +17 7578370 COSM437533 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.559+1G>T;AA=p.?;CNT=3 +17 7578370 COSM131536 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.280+1G>A;AA=p.?;CNT=2 +17 7578370 COSM44268 C A . . GENE=TP53;STRAND=-;CDS=c.559+1G>T;AA=p.?;CNT=5 +17 7578370 COSM437535 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.280+1G>T;AA=p.?;CNT=3 +17 7578370 COSM131537 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.163+1G>A;AA=p.?;CNT=2 +17 7578370 COSM437536 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.163+1G>T;AA=p.?;CNT=3 +17 7578370 COSM131534 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.559+1G>A;AA=p.?;CNT=2 +17 7578370 COSM437534 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.559+1G>T;AA=p.?;CNT=3 +17 7578374 COSM116607 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.277G>A;AA=p.D93N;CNT=1 +17 7578374 COSM116605 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.556G>A;AA=p.D186N;CNT=1 +17 7578374 COSM116606 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.160G>A;AA=p.D54N;CNT=1 +17 7578374 COSM44700 C T . . GENE=TP53;STRAND=-;CDS=c.556G>A;AA=p.D186N;CNT=1 +17 7578374 COSM116608 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.556G>A;AA=p.D186N;CNT=1 +17 7578380 COSM165078 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.550G>C;AA=p.D184H;CNT=1 +17 7578380 COSM165079 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.550G>C;AA=p.D184H;CNT=1 +17 7578380 COSM165080 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.154G>C;AA=p.D52H;CNT=1 +17 7578380 COSM165081 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.271G>C;AA=p.D91H;CNT=1 +17 7578380 COSM43797 C G . . GENE=TP53;STRAND=-;CDS=c.550G>C;AA=p.D184H;CNT=1 +17 7578381 COSM272222 TGAGCAGCGCTCATGGTGG T . . GENE=TP53;STRAND=-;CDS=c.531_548del18;AA=p.H178_S183delHHERCS;CNT=1 +17 7578381 COSM272224 TGAGCAGCGCTCATGGTGG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.531_548del18;AA=p.H178_S183delHHERCS;CNT=1 +17 7578381 COSM272223 TGAGCAGCGCTCATGGTGG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.531_548del18;AA=p.H178_S183delHHERCS;CNT=1 +17 7578381 COSM272225 TGAGCAGCGCTCATGGTGG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.135_152del18;AA=p.H46_S51delHHERCS;CNT=1 +17 7578381 COSM272226 TGAGCAGCGCTCATGGTGG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.252_269del18;AA=p.H85_S90delHHERCS;CNT=1 +17 7578382 COSM562634 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.548C>G;AA=p.S183*;CNT=2 +17 7578382 COSM562633 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.548C>G;AA=p.S183*;CNT=2 +17 7578382 COSM562635 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.269C>G;AA=p.S90*;CNT=2 +17 7578382 COSM10706 G C . . GENE=TP53;STRAND=-;CDS=c.548C>G;AA=p.S183*;CNT=2 +17 7578382 COSM562636 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.152C>G;AA=p.S51*;CNT=2 +17 7578388 COSM45046 C G . . GENE=TP53;STRAND=-;CDS=c.542G>C;AA=p.R181P;CNT=1 +17 7578389 COSM131462 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.541C>T;AA=p.R181C;CNT=1 +17 7578389 COSM131463 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.541C>T;AA=p.R181C;CNT=1 +17 7578389 COSM131465 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.145C>T;AA=p.R49C;CNT=1 +17 7578389 COSM131464 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.262C>T;AA=p.R88C;CNT=1 +17 7578389 COSM11090 G A . . GENE=TP53;STRAND=-;CDS=c.541C>T;AA=p.R181C;CNT=1 +17 7578390 COSM323932 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.261G>T;AA=p.E87D;CNT=1 +17 7578390 COSM323930 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.540G>T;AA=p.E180D;CNT=1 +17 7578390 COSM323931 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.144G>T;AA=p.E48D;CNT=1 +17 7578390 COSM323929 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.540G>T;AA=p.E180D;CNT=1 +17 7578390 COSM45372 C A . . GENE=TP53;STRAND=-;CDS=c.540G>T;AA=p.E180D;CNT=1 +17 7578391 COSM85576 TCATGG T . . GENE=TP53;STRAND=-;CDS=c.534_538delCCATG;AA=p.H178fs*6;CNT=1 +17 7578393 COSM1158095 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.537T>G;AA=p.H179Q;CNT=1 +17 7578393 COSM307266 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.258T>A;AA=p.H86Q;CNT=2 +17 7578393 COSM44214 A T . . GENE=TP53;STRAND=-;CDS=c.537T>A;AA=p.H179Q;CNT=2 +17 7578393 COSM307263 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.537T>A;AA=p.H179Q;CNT=2 +17 7578393 COSM307265 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.141T>A;AA=p.H47Q;CNT=2 +17 7578393 COSM1158096 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.258T>G;AA=p.H86Q;CNT=1 +17 7578393 COSM1158094 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.537T>G;AA=p.H179Q;CNT=1 +17 7578393 COSM307264 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.537T>A;AA=p.H179Q;CNT=2 +17 7578393 COSM1158097 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.141T>G;AA=p.H47Q;CNT=1 +17 7578393 COSM11249 A C . . GENE=TP53;STRAND=-;CDS=c.537T>G;AA=p.H179Q;CNT=2 +17 7578394 COSM214225 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.257A>G;AA=p.H86R;CNT=2 +17 7578394 COSM129847 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.140A>T;AA=p.H47L;CNT=4 +17 7578394 COSM214224 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.140A>G;AA=p.H47R;CNT=2 +17 7578394 COSM129845 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.536A>T;AA=p.H179L;CNT=4 +17 7578394 COSM129846 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.257A>T;AA=p.H86L;CNT=4 +17 7578394 COSM129844 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.536A>T;AA=p.H179L;CNT=4 +17 7578394 COSM214222 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.536A>G;AA=p.H179R;CNT=2 +17 7578394 COSM43635 T A . . GENE=TP53;STRAND=-;CDS=c.536A>T;AA=p.H179L;CNT=4 +17 7578394 COSM214223 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.536A>G;AA=p.H179R;CNT=2 +17 7578394 COSM10889 T C . . GENE=TP53;STRAND=-;CDS=c.536A>G;AA=p.H179R;CNT=7 +17 7578395 COSM326728 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.535C>A;AA=p.H179N;CNT=1 +17 7578395 COSM326730 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.256C>A;AA=p.H86N;CNT=1 +17 7578395 COSM707884 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.535C>G;AA=p.H179D;CNT=1 +17 7578395 COSM129848 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.535C>T;AA=p.H179Y;CNT=5 +17 7578395 COSM44151 G T . . GENE=TP53;STRAND=-;CDS=c.535C>A;AA=p.H179N;CNT=1 +17 7578395 COSM129849 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.535C>T;AA=p.H179Y;CNT=5 +17 7578395 COSM10768 G A . . GENE=TP53;STRAND=-;CDS=c.535C>T;AA=p.H179Y;CNT=5 +17 7578395 COSM129850 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.256C>T;AA=p.H86Y;CNT=5 +17 7578395 COSM326727 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.535C>A;AA=p.H179N;CNT=1 +17 7578395 COSM129851 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.139C>T;AA=p.H47Y;CNT=5 +17 7578395 COSM326729 G T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.139C>A;AA=p.H47N;CNT=1 +17 7578395 COSM707885 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.535C>G;AA=p.H179D;CNT=1 +17 7578395 COSM707886 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.256C>G;AA=p.H86D;CNT=1 +17 7578395 COSM707887 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.139C>G;AA=p.H47D;CNT=1 +17 7578395 COSM44776 G C . . GENE=TP53;STRAND=-;CDS=c.535C>G;AA=p.H179D;CNT=1 +17 7578397 COSM44659 TG T . . GENE=TP53;STRAND=-;CDS=c.532delC;AA=p.H178fs*69;CNT=2 +17 7578397 COSM111498 TG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.532delC;AA=p.H178fs*69;CNT=2 +17 7578397 COSM111495 TG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.532delC;AA=p.H178fs*69;CNT=2 +17 7578397 COSM111496 TG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.136delC;AA=p.H46fs*>45;CNT=2 +17 7578397 COSM111497 TG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.253delC;AA=p.H85fs*69;CNT=2 +17 7578398 COSM44901 G C . . GENE=TP53;STRAND=-;CDS=c.532C>G;AA=p.H178D;CNT=1 +17 7578398 COSM984946 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.532C>G;AA=p.H178D;CNT=1 +17 7578398 COSM984949 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.253C>G;AA=p.H85D;CNT=1 +17 7578398 COSM984950 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.136C>G;AA=p.H46D;CNT=1 +17 7578398 COSM984948 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.532C>G;AA=p.H178D;CNT=1 +17 7578400 COSM117221 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.530C>G;AA=p.P177R;CNT=1 +17 7578400 COSM117222 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.134C>G;AA=p.P45R;CNT=1 +17 7578400 COSM10651 G C . . GENE=TP53;STRAND=-;CDS=c.530C>G;AA=p.P177R;CNT=1 +17 7578400 COSM117223 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.251C>G;AA=p.P84R;CNT=1 +17 7578400 COSM117224 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.530C>G;AA=p.P177R;CNT=1 +17 7578402 COSM179824 G T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.132C>A;AA=p.C44*;CNT=2 +17 7578402 COSM43734 G T . . GENE=TP53;STRAND=-;CDS=c.528C>A;AA=p.C176*;CNT=2 +17 7578402 COSM179823 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.528C>A;AA=p.C176*;CNT=2 +17 7578402 COSM179822 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.528C>A;AA=p.C176*;CNT=2 +17 7578402 COSM179825 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.249C>A;AA=p.C83*;CNT=2 +17 7578403 COSM10645 C A . . GENE=TP53;STRAND=-;CDS=c.527G>T;AA=p.C176F;CNT=13 +17 7578403 COSM99672 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.527G>A;AA=p.C176Y;CNT=4 +17 7578403 COSM10687 C T . . GENE=TP53;STRAND=-;CDS=c.527G>A;AA=p.C176Y;CNT=9 +17 7578403 COSM117398 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.527G>T;AA=p.C176F;CNT=13 +17 7578403 COSM99670 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.131G>A;AA=p.C44Y;CNT=4 +17 7578403 COSM117395 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.527G>T;AA=p.C176F;CNT=13 +17 7578403 COSM99671 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.248G>A;AA=p.C83Y;CNT=4 +17 7578403 COSM99669 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.527G>A;AA=p.C176Y;CNT=4 +17 7578403 COSM117397 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.248G>T;AA=p.C83F;CNT=13 +17 7578403 COSM117396 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.131G>T;AA=p.C44F;CNT=13 +17 7578404 COSM220760 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.247T>G;AA=p.C83G;CNT=1 +17 7578404 COSM44692 A C . . GENE=TP53;STRAND=-;CDS=c.526T>G;AA=p.C176G;CNT=1 +17 7578404 COSM220759 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.130T>G;AA=p.C44G;CNT=1 +17 7578404 COSM220758 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.526T>G;AA=p.C176G;CNT=1 +17 7578404 COSM220757 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.526T>G;AA=p.C176G;CNT=1 +17 7578406 COSM99914 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.524G>A;AA=p.R175H;CNT=40 +17 7578406 COSM99024 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.245G>A;AA=p.R82H;CNT=41 +17 7578406 COSM10648 C T . . GENE=TP53;STRAND=-;CDS=c.524G>A;AA=p.R175H;CNT=50 +17 7578406 COSM99023 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.128G>A;AA=p.R43H;CNT=41 +17 7578406 COSM99022 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.524G>A;AA=p.R175H;CNT=40 +17 7578407 COSM179829 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.244C>T;AA=p.R82C;CNT=2 +17 7578407 COSM179827 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.523C>T;AA=p.R175C;CNT=2 +17 7578407 COSM707882 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.244C>G;AA=p.R82G;CNT=3 +17 7578407 COSM707880 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.523C>G;AA=p.R175G;CNT=3 +17 7578407 COSM707883 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.127C>G;AA=p.R43G;CNT=3 +17 7578407 COSM43680 G A . . GENE=TP53;STRAND=-;CDS=c.523C>T;AA=p.R175C;CNT=2 +17 7578407 COSM10870 G C . . GENE=TP53;STRAND=-;CDS=c.523C>G;AA=p.R175G;CNT=3 +17 7578407 COSM179828 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.127C>T;AA=p.R43C;CNT=2 +17 7578407 COSM179826 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.523C>T;AA=p.R175C;CNT=2 +17 7578407 COSM707881 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.523C>G;AA=p.R175G;CNT=3 +17 7578410 COSM298209 TCA T . . GENE=TP53;STRAND=-;CDS=c.518_519delTG;AA=p.V173fs*7;CNT=1 +17 7578410 COSM298211 TCA T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.518_519delTG;AA=p.V173fs*7;CNT=1 +17 7578410 COSM298210 TCA T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.518_519delTG;AA=p.V173fs*7;CNT=1 +17 7578410 COSM298212 TCA T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.122_123delTG;AA=p.V41fs*7;CNT=1 +17 7578410 COSM298213 TCA T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.239_240delTG;AA=p.V80fs*7;CNT=1 +17 7578413 COSM44057 C G . . GENE=TP53;STRAND=-;CDS=c.517G>C;AA=p.V173L;CNT=2 +17 7578413 COSM121043 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.517G>C;AA=p.V173L;CNT=2 +17 7578413 COSM121044 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.238G>C;AA=p.V80L;CNT=2 +17 7578413 COSM98966 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.238G>A;AA=p.V80M;CNT=2 +17 7578413 COSM99639 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.121G>T;AA=p.V41L;CNT=4 +17 7578413 COSM98964 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.517G>A;AA=p.V173M;CNT=2 +17 7578413 COSM99641 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.517G>T;AA=p.V173L;CNT=4 +17 7578413 COSM11084 C T . . GENE=TP53;STRAND=-;CDS=c.517G>A;AA=p.V173M;CNT=3 +17 7578413 COSM43559 C A . . GENE=TP53;STRAND=-;CDS=c.517G>T;AA=p.V173L;CNT=4 +17 7578413 COSM121042 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.517G>C;AA=p.V173L;CNT=2 +17 7578413 COSM121041 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.517G>A;AA=p.V173M;CNT=2 +17 7578413 COSM99640 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.238G>T;AA=p.V80L;CNT=4 +17 7578413 COSM99638 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.517G>T;AA=p.V173L;CNT=4 +17 7578413 COSM98965 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.121G>A;AA=p.V41M;CNT=2 +17 7578413 COSM121045 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.121G>C;AA=p.V41L;CNT=2 +17 7578415 COSM707878 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.236T>G;AA=p.V79G;CNT=1 +17 7578415 COSM1161214 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.515T>A;AA=p.V172D;CNT=1 +17 7578415 COSM707877 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.515T>G;AA=p.V172G;CNT=1 +17 7578415 COSM1161215 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.236T>A;AA=p.V79D;CNT=1 +17 7578415 COSM1161213 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.515T>A;AA=p.V172D;CNT=1 +17 7578415 COSM45047 A C . . GENE=TP53;STRAND=-;CDS=c.515T>G;AA=p.V172G;CNT=1 +17 7578415 COSM707876 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.515T>G;AA=p.V172G;CNT=1 +17 7578415 COSM44229 A T . . GENE=TP53;STRAND=-;CDS=c.515T>A;AA=p.V172D;CNT=1 +17 7578415 COSM707879 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.119T>G;AA=p.V40G;CNT=1 +17 7578415 COSM1161216 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.119T>A;AA=p.V40D;CNT=1 +17 7578415 COSM437546 ACCTC A . . GENE=TP53;STRAND=-;CDS=c.511_514delGAGG;AA=p.E171fs*2;CNT=1 +17 7578415 COSM437547 ACCTC A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.511_514delGAGG;AA=p.E171fs*2;CNT=1 +17 7578415 COSM437548 ACCTC A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.511_514delGAGG;AA=p.E171fs*2;CNT=1 +17 7578415 COSM437550 ACCTC A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.115_118delGAGG;AA=p.E39fs*2;CNT=1 +17 7578415 COSM437549 ACCTC A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.232_235delGAGG;AA=p.E78fs*2;CNT=1 +17 7578416 COSM354842 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.118G>T;AA=p.V40F;CNT=2 +17 7578416 COSM44240 C A . . GENE=TP53;STRAND=-;CDS=c.514G>T;AA=p.V172F;CNT=2 +17 7578416 COSM354841 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.235G>T;AA=p.V79F;CNT=2 +17 7578416 COSM354839 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.514G>T;AA=p.V172F;CNT=2 +17 7578416 COSM354840 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.514G>T;AA=p.V172F;CNT=2 +17 7578419 COSM417965 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.511G>A;AA=p.E171K;CNT=1 +17 7578419 COSM44312 C T . . GENE=TP53;STRAND=-;CDS=c.511G>A;AA=p.E171K;CNT=1 +17 7578419 COSM10996 C A . . GENE=TP53;STRAND=-;CDS=c.511G>T;AA=p.E171*;CNT=1 +17 7578419 COSM357725 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.232G>T;AA=p.E78*;CNT=1 +17 7578419 COSM417966 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.232G>A;AA=p.E78K;CNT=1 +17 7578419 COSM357726 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.115G>T;AA=p.E39*;CNT=1 +17 7578419 COSM417964 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.511G>A;AA=p.E171K;CNT=1 +17 7578419 COSM417967 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.115G>A;AA=p.E39K;CNT=1 +17 7578419 COSM357724 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.511G>T;AA=p.E171*;CNT=1 +17 7578419 COSM357723 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.511G>T;AA=p.E171*;CNT=1 +17 7578423 COSM357728 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.507G>A;AA=p.M169I;CNT=1 +17 7578423 COSM357727 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.507G>A;AA=p.M169I;CNT=1 +17 7578423 COSM357730 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.111G>A;AA=p.M37I;CNT=1 +17 7578423 COSM44126 C T . . GENE=TP53;STRAND=-;CDS=c.507G>A;AA=p.M169I;CNT=1 +17 7578423 COSM357729 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.228G>A;AA=p.M76I;CNT=1 +17 7578427 COSM562629 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.503A>T;AA=p.H168L;CNT=1 +17 7578427 COSM562632 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.107A>T;AA=p.H36L;CNT=1 +17 7578427 COSM44801 T A . . GENE=TP53;STRAND=-;CDS=c.503A>T;AA=p.H168L;CNT=1 +17 7578427 COSM562630 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.503A>T;AA=p.H168L;CNT=1 +17 7578427 COSM562631 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.224A>T;AA=p.H75L;CNT=1 +17 7578428 COSM437555 GC G . . GENE=TP53;STRAND=-;CDS=c.501delG;AA=p.Q167fs*3;CNT=1 +17 7578428 COSM437556 GC G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.501delG;AA=p.Q167fs*3;CNT=1 +17 7578428 COSM437557 GC G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.501delG;AA=p.Q167fs*3;CNT=1 +17 7578428 COSM437559 GC G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.105delG;AA=p.Q35fs*3;CNT=1 +17 7578428 COSM437558 GC G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.222delG;AA=p.Q74fs*3;CNT=1 +17 7578429 COSM44275 CTG C . . GENE=TP53;STRAND=-;CDS=c.499_500delCA;AA=p.Q167fs*13;CNT=1 +17 7578429 COSM405173 CTG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.499_500delCA;AA=p.Q167fs*13;CNT=1 +17 7578429 COSM405174 CTG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.499_500delCA;AA=p.Q167fs*13;CNT=1 +17 7578429 COSM405176 CTG C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.103_104delCA;AA=p.Q35fs*13;CNT=1 +17 7578429 COSM405175 CTG C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.220_221delCA;AA=p.Q74fs*13;CNT=1 +17 7578431 COSM121082 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.499C>T;AA=p.Q167*;CNT=1 +17 7578431 COSM121081 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.499C>T;AA=p.Q167*;CNT=1 +17 7578431 COSM11333 G A . . GENE=TP53;STRAND=-;CDS=c.499C>T;AA=p.Q167*;CNT=1 +17 7578431 COSM121083 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.220C>T;AA=p.Q74*;CNT=1 +17 7578431 COSM121084 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.103C>T;AA=p.Q35*;CNT=1 +17 7578431 COSM69214 G GT . . GENE=TP53;STRAND=-;CDS=c.498_499insA;AA=p.Q167fs*14;CNT=1 +17 7578432 COSM51646 T TG . . GENE=TP53;STRAND=-;CDS=c.497_498insC;AA=p.Q167fs*14;CNT=3 +17 7578433 COSM369075 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.497C>G;AA=p.S166*;CNT=3 +17 7578433 COSM44467 G C . . GENE=TP53;STRAND=-;CDS=c.497C>G;AA=p.S166*;CNT=3 +17 7578433 COSM369076 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.218C>G;AA=p.S73*;CNT=3 +17 7578433 COSM369074 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.497C>G;AA=p.S166*;CNT=3 +17 7578433 COSM369077 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.101C>G;AA=p.S34*;CNT=3 +17 7578437 COSM1172489 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.493C>T;AA=p.Q165*;CNT=1 +17 7578437 COSM1172490 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.214C>T;AA=p.Q72*;CNT=1 +17 7578437 COSM43632 G A . . GENE=TP53;STRAND=-;CDS=c.493C>T;AA=p.Q165*;CNT=1 +17 7578437 COSM1172488 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.493C>T;AA=p.Q165*;CNT=1 +17 7578437 COSM1172491 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.97C>T;AA=p.Q33*;CNT=1 +17 7578438 COSM1194559 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.96G>T;AA=p.K32N;CNT=1 +17 7578438 COSM1194557 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.492G>T;AA=p.K164N;CNT=1 +17 7578438 COSM1194556 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.492G>T;AA=p.K164N;CNT=1 +17 7578438 COSM1194558 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.213G>T;AA=p.K71N;CNT=1 +17 7578438 COSM11369 C A . . GENE=TP53;STRAND=-;CDS=c.492G>T;AA=p.K164N;CNT=1 +17 7578440 COSM380907 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.94A>T;AA=p.K32*;CNT=1 +17 7578440 COSM380905 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.490A>T;AA=p.K164*;CNT=1 +17 7578440 COSM10750 T A . . GENE=TP53;STRAND=-;CDS=c.490A>T;AA=p.K164*;CNT=1 +17 7578440 COSM707874 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.211A>G;AA=p.K71E;CNT=1 +17 7578440 COSM380904 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.490A>T;AA=p.K164*;CNT=1 +17 7578440 COSM380906 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.211A>T;AA=p.K71*;CNT=1 +17 7578440 COSM707872 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.490A>G;AA=p.K164E;CNT=1 +17 7578440 COSM707875 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.94A>G;AA=p.K32E;CNT=1 +17 7578440 COSM707873 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.490A>G;AA=p.K164E;CNT=1 +17 7578440 COSM10762 T C . . GENE=TP53;STRAND=-;CDS=c.490A>G;AA=p.K164E;CNT=2 +17 7578442 COSM129852 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.488A>G;AA=p.Y163C;CNT=11 +17 7578442 COSM10808 T C . . GENE=TP53;STRAND=-;CDS=c.488A>G;AA=p.Y163C;CNT=16 +17 7578442 COSM129854 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.209A>G;AA=p.Y70C;CNT=11 +17 7578442 COSM129855 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.92A>G;AA=p.Y31C;CNT=11 +17 7578442 COSM129853 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.488A>G;AA=p.Y163C;CNT=11 +17 7578442 COSM437560 TAGA T . . GENE=TP53;STRAND=-;CDS=c.485_487delTCT;AA=p.I162_Y163>N;CNT=1 +17 7578442 COSM437561 TAGA T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.485_487delTCT;AA=p.I162_Y163>N;CNT=1 +17 7578442 COSM437562 TAGA T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.485_487delTCT;AA=p.I162_Y163>N;CNT=1 +17 7578442 COSM437564 TAGA T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.89_91delTCT;AA=p.I30_Y31>N;CNT=1 +17 7578442 COSM437563 TAGA T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.206_208delTCT;AA=p.I69_Y70>N;CNT=1 +17 7578443 COSM226792 A C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.91T>G;AA=p.Y31D;CNT=2 +17 7578443 COSM226793 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.208T>G;AA=p.Y70D;CNT=2 +17 7578443 COSM44216 A C . . GENE=TP53;STRAND=-;CDS=c.487T>G;AA=p.Y163D;CNT=2 +17 7578443 COSM44623 A T . . GENE=TP53;STRAND=-;CDS=c.487T>A;AA=p.Y163N;CNT=2 +17 7578443 COSM307268 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.487T>A;AA=p.Y163N;CNT=1 +17 7578443 COSM307270 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.208T>A;AA=p.Y70N;CNT=1 +17 7578443 COSM43846 A G . . GENE=TP53;STRAND=-;CDS=c.487T>C;AA=p.Y163H;CNT=1 +17 7578443 COSM307269 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.91T>A;AA=p.Y31N;CNT=1 +17 7578443 COSM307267 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.487T>A;AA=p.Y163N;CNT=1 +17 7578443 COSM226791 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.487T>G;AA=p.Y163D;CNT=2 +17 7578443 COSM226790 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.487T>G;AA=p.Y163D;CNT=2 +17 7578445 COSM11966 A T . . GENE=TP53;STRAND=-;CDS=c.485T>A;AA=p.I162N;CNT=2 +17 7578445 COSM327539 A T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.89T>A;AA=p.I30N;CNT=2 +17 7578445 COSM327538 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.485T>A;AA=p.I162N;CNT=2 +17 7578445 COSM327537 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.485T>A;AA=p.I162N;CNT=2 +17 7578445 COSM327540 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.206T>A;AA=p.I69N;CNT=2 +17 7578446 COSM437566 T TN . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.483_484insTGGCC;AA=p.I162fs*10;CNT=1 +17 7578446 COSM437568 T TN . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.204_205insTGGCC;AA=p.I69fs*10;CNT=1 +17 7578446 COSM437565 T TN . . GENE=TP53;STRAND=-;CDS=c.483_484insTGGCC;AA=p.I162fs*10;CNT=1 +17 7578446 COSM437569 T TN . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.87_88insTGGCC;AA=p.I30fs*10;CNT=1 +17 7578446 COSM437567 T TN . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.483_484insTGGCC;AA=p.I162fs*10;CNT=1 +17 7578448 COSM85575 GCCATGGCGCGGACGCGGG G . . GENE=TP53;STRAND=-;CDS=c.464_481del18;AA=p.R156_A161del;CNT=1 +17 7578449 COSM249096 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.85G>A;AA=p.A29T;CNT=4 +17 7578449 COSM10739 C T . . GENE=TP53;STRAND=-;CDS=c.481G>A;AA=p.A161T;CNT=4 +17 7578449 COSM249094 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.481G>A;AA=p.A161T;CNT=4 +17 7578449 COSM249095 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.481G>A;AA=p.A161T;CNT=4 +17 7578449 COSM249097 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.202G>A;AA=p.A68T;CNT=4 +17 7578450 COSM1158488 CA C . . GENE=TP53;STRAND=-;CDS=c.479delT;AA=p.M160fs*10;CNT=1 +17 7578450 COSM1158489 CA C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.479delT;AA=p.M160fs*10;CNT=1 +17 7578450 COSM1158490 CA C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.479delT;AA=p.M160fs*10;CNT=1 +17 7578450 COSM1158492 CA C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.83delT;AA=p.M28fs*10;CNT=1 +17 7578450 COSM1158491 CA C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.200delT;AA=p.M67fs*10;CNT=1 +17 7578452 COSM306853 TGGCGCG TGG . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.76_81CGCGCC>CC;AA=p.R26fs;CNT=2 +17 7578452 COSM306851 TGGCGCG TGG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.472_477CGCGCC>CC;AA=p.R158fs;CNT=2 +17 7578452 COSM306850 TGGCGCG TGG . . GENE=TP53;STRAND=-;CDS=c.472_477CGCGCC>CC;AA=p.R158fs*11;CNT=2 +17 7578452 COSM306852 TGGCGCG TGG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.472_477CGCGCC>CC;AA=p.R158fs;CNT=2 +17 7578452 COSM306854 TGGCGCG TGG . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.193_198CGCGCC>CC;AA=p.R65fs;CNT=2 +17 7578452 COSM405129 TGGCGCGGACG T . . GENE=TP53;STRAND=-;CDS=c.468_477del10;AA=p.V157fs*10;CNT=1 +17 7578452 COSM405130 TGGCGCGGACG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.468_477del10;AA=p.V157fs*10;CNT=1 +17 7578452 COSM405131 TGGCGCGGACG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.468_477del10;AA=p.V157fs*10;CNT=1 +17 7578452 COSM405133 TGGCGCGGACG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.72_81del10;AA=p.V25fs*10;CNT=1 +17 7578452 COSM405132 TGGCGCGGACG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.189_198del10;AA=p.V64fs*10;CNT=1 +17 7578454 COSM288919 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.476C>T;AA=p.A159V;CNT=4 +17 7578454 COSM11148 G A . . GENE=TP53;STRAND=-;CDS=c.476C>T;AA=p.A159V;CNT=6 +17 7578454 COSM288922 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.197C>T;AA=p.A66V;CNT=4 +17 7578454 COSM288920 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.476C>T;AA=p.A159V;CNT=4 +17 7578454 COSM288921 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.80C>T;AA=p.A27V;CNT=4 +17 7578454 COSM43831 GCGCG G . . GENE=TP53;STRAND=-;CDS=c.472_475delCGCG;AA=p.R158fs*11;CNT=1 +17 7578454 COSM215724 GCGCG G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.472_475delCGCG;AA=p.R158fs*11;CNT=1 +17 7578454 COSM215723 GCGCG G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.472_475delCGCG;AA=p.R158fs*11;CNT=1 +17 7578454 COSM215725 GCGCG G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.76_79delCGCG;AA=p.R26fs*11;CNT=1 +17 7578454 COSM215726 GCGCG G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.193_196delCGCG;AA=p.R65fs*11;CNT=1 +17 7578455 COSM562627 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.196G>C;AA=p.A66P;CNT=2 +17 7578455 COSM45286 C A . . GENE=TP53;STRAND=-;CDS=c.475G>T;AA=p.A159S;CNT=1 +17 7578455 COSM43836 C G . . GENE=TP53;STRAND=-;CDS=c.475G>C;AA=p.A159P;CNT=2 +17 7578455 COSM1177659 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.79G>T;AA=p.A27S;CNT=1 +17 7578455 COSM1177657 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.475G>T;AA=p.A159S;CNT=1 +17 7578455 COSM562625 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.475G>C;AA=p.A159P;CNT=2 +17 7578455 COSM1177658 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.196G>T;AA=p.A66S;CNT=1 +17 7578455 COSM1177656 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.475G>T;AA=p.A159S;CNT=1 +17 7578455 COSM562628 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.79G>C;AA=p.A27P;CNT=2 +17 7578455 COSM562626 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.475G>C;AA=p.A159P;CNT=2 +17 7578457 COSM220779 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.473G>A;AA=p.R158H;CNT=5 +17 7578457 COSM10690 C T . . GENE=TP53;STRAND=-;CDS=c.473G>A;AA=p.R158H;CNT=5 +17 7578457 COSM220778 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.473G>A;AA=p.R158H;CNT=5 +17 7578457 COSM99675 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.473G>T;AA=p.R158L;CNT=13 +17 7578457 COSM10714 C A . . GENE=TP53;STRAND=-;CDS=c.473G>T;AA=p.R158L;CNT=13 +17 7578457 COSM99678 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.473G>T;AA=p.R158L;CNT=13 +17 7578457 COSM99676 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.77G>T;AA=p.R26L;CNT=13 +17 7578457 COSM99677 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.194G>T;AA=p.R65L;CNT=13 +17 7578457 COSM220780 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.77G>A;AA=p.R26H;CNT=5 +17 7578457 COSM220781 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.194G>A;AA=p.R65H;CNT=5 +17 7578458 COSM318151 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.472C>G;AA=p.R158G;CNT=2 +17 7578458 COSM318152 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.472C>G;AA=p.R158G;CNT=2 +17 7578458 COSM318154 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.193C>G;AA=p.R65G;CNT=2 +17 7578458 COSM11087 G C . . GENE=TP53;STRAND=-;CDS=c.472C>G;AA=p.R158G;CNT=2 +17 7578458 COSM318153 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.76C>G;AA=p.R26G;CNT=2 +17 7578461 COSM131480 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.469G>T;AA=p.V157F;CNT=9 +17 7578461 COSM10670 C A . . GENE=TP53;STRAND=-;CDS=c.469G>T;AA=p.V157F;CNT=14 +17 7578461 COSM131482 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.190G>T;AA=p.V64F;CNT=9 +17 7578461 COSM131483 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.73G>T;AA=p.V25F;CNT=9 +17 7578461 COSM131481 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.469G>T;AA=p.V157F;CNT=9 +17 7578461 COSM1157909 CGCGGGTGCCGGGCG C . . GENE=TP53;STRAND=-;CDS=c.455_468del14;AA=p.P152fs*24;CNT=1 +17 7578461 COSM1157910 CGCGGGTGCCGGGCG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.455_468del14;AA=p.P152fs*24;CNT=1 +17 7578461 COSM1157911 CGCGGGTGCCGGGCG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.455_468del14;AA=p.P152fs*24;CNT=1 +17 7578461 COSM1157913 CGCGGGTGCCGGGCG C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.59_72del14;AA=p.P20fs*24;CNT=1 +17 7578461 COSM1157912 CGCGGGTGCCGGGCG C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.176_189del14;AA=p.P59fs*24;CNT=1 +17 7578462 COSM250017 GCGGGTGCCGGGCGGGGGTGT G . . GENE=TP53;STRAND=-;CDS=c.468_487del?;AA=p.?;CNT=1 +17 7578462 COSM250019 GCGGGTGCCGGGCGGGGGTGT G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.468_487del?;AA=p.?;CNT=1 +17 7578462 COSM250018 GCGGGTGCCGGGCGGGGGTGT G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.468_487del?;AA=p.?;CNT=1 +17 7578462 COSM250020 GCGGGTGCCGGGCGGGGGTGT G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.93_112del?;AA=p.?;CNT=1 +17 7578462 COSM250021 GCGGGTGCCGGGCGGGGGTGT G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.189_208del?;AA=p.?;CNT=1 +17 7578463 COSM10760 C G . . GENE=TP53;STRAND=-;CDS=c.467G>C;AA=p.R156P;CNT=1 +17 7578466 COSM213311 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.464C>A;AA=p.T155N;CNT=1 +17 7578466 COSM562621 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.464C>T;AA=p.T155I;CNT=1 +17 7578466 COSM213313 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.185C>A;AA=p.T62N;CNT=1 +17 7578466 COSM562623 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.185C>T;AA=p.T62I;CNT=1 +17 7578466 COSM213310 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.464C>A;AA=p.T155N;CNT=1 +17 7578466 COSM11218 G T . . GENE=TP53;STRAND=-;CDS=c.464C>A;AA=p.T155N;CNT=1 +17 7578466 COSM44033 G A . . GENE=TP53;STRAND=-;CDS=c.464C>T;AA=p.T155I;CNT=1 +17 7578466 COSM562624 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.68C>T;AA=p.T23I;CNT=1 +17 7578466 COSM562622 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.464C>T;AA=p.T155I;CNT=1 +17 7578466 COSM213312 G T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.68C>A;AA=p.T23N;CNT=1 +17 7578467 COSM44303 T C . . GENE=TP53;STRAND=-;CDS=c.463A>G;AA=p.T155A;CNT=1 +17 7578467 COSM117049 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.463A>G;AA=p.T155A;CNT=1 +17 7578467 COSM357533 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.184A>C;AA=p.T62P;CNT=2 +17 7578467 COSM357534 T G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.67A>C;AA=p.T23P;CNT=2 +17 7578467 COSM117051 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.184A>G;AA=p.T62A;CNT=1 +17 7578467 COSM10912 T G . . GENE=TP53;STRAND=-;CDS=c.463A>C;AA=p.T155P;CNT=2 +17 7578467 COSM117050 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.67A>G;AA=p.T23A;CNT=1 +17 7578467 COSM357531 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.463A>C;AA=p.T155P;CNT=2 +17 7578467 COSM357532 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.463A>C;AA=p.T155P;CNT=2 +17 7578467 COSM117052 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.463A>G;AA=p.T155A;CNT=1 +17 7578468 COSM111973 G GCCGGGCGGGGGTGTGGAATCAGTG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.461_462ins24;AA=p.T155_R156insDSTPPPGT;CNT=1 +17 7578468 COSM111975 G GCCGGGCGGGGGTGTGGAATCAGTG . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.182_183ins24;AA=p.T62_R63insDSTPPPGT;CNT=1 +17 7578468 COSM111976 G GCCGGGCGGGGGTGTGGAATCAGTG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.461_462ins24;AA=p.T155_R156insDSTPPPGT;CNT=1 +17 7578468 COSM111972 G GCCGGGCGGGGGTGTGGAATCAGTG . . GENE=TP53;STRAND=-;CDS=c.461_462ins24;AA=p.T155_R156insDSTPPPGT;CNT=1 +17 7578468 COSM111974 G GCCGGGCGGGGGTGTGGAATCAGTG . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.65_66ins24;AA=p.T23_R24insDSTPPPGT;CNT=1 +17 7578469 COSM342245 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.182G>T;AA=p.G61V;CNT=5 +17 7578469 COSM6815 C A . . GENE=TP53;STRAND=-;CDS=c.461G>T;AA=p.G154V;CNT=5 +17 7578469 COSM342244 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.461G>T;AA=p.G154V;CNT=5 +17 7578469 COSM342246 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.65G>T;AA=p.G22V;CNT=5 +17 7578469 COSM342243 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.461G>T;AA=p.G154V;CNT=5 +17 7578469 COSM69087 CCGGGCGGGGGTGTGGAATCAACCCACAGCTG C . . GENE=TP53;STRAND=-;CDS=c.430_460del31;AA=p.Q144fs*16;CNT=1 +17 7578469 COSM111416 CCGGGCGGGGGTGT C . . GENE=TP53;STRAND=-;CDS=c.448_460del13;AA=p.T150fs*16;CNT=1 +17 7578469 COSM111420 CCGGGCGGGGGTGT C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.448_460del13;AA=p.T150fs*16;CNT=1 +17 7578469 COSM111417 CCGGGCGGGGGTGT C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.448_460del13;AA=p.T150fs*16;CNT=1 +17 7578469 COSM111418 CCGGGCGGGGGTGT C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.52_64del13;AA=p.T18fs*16;CNT=1 +17 7578469 COSM111419 CCGGGCGGGGGTGT C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.169_181del13;AA=p.T57fs*16;CNT=1 +17 7578470 COSM167465 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.181G>T;AA=p.G61C;CNT=1 +17 7578470 COSM167463 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.460G>T;AA=p.G154C;CNT=1 +17 7578470 COSM167462 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.460G>T;AA=p.G154C;CNT=1 +17 7578470 COSM167464 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.64G>T;AA=p.G22C;CNT=1 +17 7578470 COSM44715 C A . . GENE=TP53;STRAND=-;CDS=c.460G>T;AA=p.G154C;CNT=1 +17 7578470 COSM404850 CG C . . GENE=TP53;STRAND=-;CDS=c.459delC;AA=p.G154fs*16;CNT=1 +17 7578470 COSM404851 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.459delC;AA=p.G154fs*16;CNT=1 +17 7578470 COSM404852 CG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.459delC;AA=p.G154fs*16;CNT=1 +17 7578470 COSM404854 CG C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.63delC;AA=p.G22fs*16;CNT=1 +17 7578470 COSM404853 CG C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.180delC;AA=p.G61fs*16;CNT=1 +17 7578473 COSM392240 G GN . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.456_457insT;AA=p.P153fs*28;CNT=1 +17 7578473 COSM392242 G GN . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.177_178insT;AA=p.P60fs*28;CNT=1 +17 7578473 COSM392239 G GN . . GENE=TP53;STRAND=-;CDS=c.456_457insT;AA=p.P153fs*28;CNT=1 +17 7578473 COSM392241 G GN . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.456_457insT;AA=p.P153fs*28;CNT=1 +17 7578473 COSM392243 G GN . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.60_61insT;AA=p.P21fs*28;CNT=1 +17 7578474 COSM43792 CG C . . GENE=TP53;STRAND=-;CDS=c.455delC;AA=p.P152fs*18;CNT=2 +17 7578474 COSM1180849 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.455delC;AA=p.P152fs*18;CNT=2 +17 7578474 COSM1180850 CG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.455delC;AA=p.P152fs*18;CNT=2 +17 7578474 COSM1180852 CG C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.59delC;AA=p.P20fs*18;CNT=2 +17 7578474 COSM1180851 CG C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.176delC;AA=p.P59fs*18;CNT=2 +17 7578475 COSM171825 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.176C>G;AA=p.P59R;CNT=1 +17 7578475 COSM129858 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.176C>T;AA=p.P59L;CNT=3 +17 7578475 COSM129859 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.59C>T;AA=p.P20L;CNT=3 +17 7578475 COSM129856 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.455C>T;AA=p.P152L;CNT=3 +17 7578475 COSM10790 G A . . GENE=TP53;STRAND=-;CDS=c.455C>T;AA=p.P152L;CNT=3 +17 7578475 COSM171823 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.455C>G;AA=p.P152R;CNT=1 +17 7578475 COSM171822 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.455C>G;AA=p.P152R;CNT=1 +17 7578475 COSM45505 G C . . GENE=TP53;STRAND=-;CDS=c.455C>G;AA=p.P152R;CNT=1 +17 7578475 COSM171824 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.59C>G;AA=p.P20R;CNT=1 +17 7578475 COSM129857 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.455C>T;AA=p.P152L;CNT=3 +17 7578478 COSM707869 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.452C>G;AA=p.P151R;CNT=1 +17 7578478 COSM259152 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.173C>A;AA=p.P58H;CNT=3 +17 7578478 COSM259151 G T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.56C>A;AA=p.P19H;CNT=3 +17 7578478 COSM707871 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.56C>G;AA=p.P19R;CNT=1 +17 7578478 COSM707868 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.452C>G;AA=p.P151R;CNT=1 +17 7578478 COSM707870 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.173C>G;AA=p.P58R;CNT=1 +17 7578478 COSM44003 G C . . GENE=TP53;STRAND=-;CDS=c.452C>G;AA=p.P151R;CNT=1 +17 7578478 COSM11476 G T . . GENE=TP53;STRAND=-;CDS=c.452C>A;AA=p.P151H;CNT=3 +17 7578478 COSM259149 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.452C>A;AA=p.P151H;CNT=3 +17 7578478 COSM259150 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.452C>A;AA=p.P151H;CNT=3 +17 7578479 COSM121049 G T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.55C>A;AA=p.P19T;CNT=1 +17 7578479 COSM99682 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.451C>G;AA=p.P151A;CNT=1 +17 7578479 COSM121048 G T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.172C>A;AA=p.P58T;CNT=1 +17 7578479 COSM984963 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.55C>T;AA=p.P19S;CNT=2 +17 7578479 COSM10905 G A . . GENE=TP53;STRAND=-;CDS=c.451C>T;AA=p.P151S;CNT=3 +17 7578479 COSM121047 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.451C>A;AA=p.P151T;CNT=1 +17 7578479 COSM121046 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.451C>A;AA=p.P151T;CNT=1 +17 7578479 COSM43911 G T . . GENE=TP53;STRAND=-;CDS=c.451C>A;AA=p.P151T;CNT=1 +17 7578479 COSM44944 G C . . GENE=TP53;STRAND=-;CDS=c.451C>G;AA=p.P151A;CNT=1 +17 7578479 COSM984959 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.451C>T;AA=p.P151S;CNT=2 +17 7578479 COSM99681 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.172C>G;AA=p.P58A;CNT=1 +17 7578479 COSM984961 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.451C>T;AA=p.P151S;CNT=2 +17 7578479 COSM99680 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.55C>G;AA=p.P19A;CNT=1 +17 7578479 COSM984962 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.172C>T;AA=p.P58S;CNT=2 +17 7578479 COSM99679 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.451C>G;AA=p.P151A;CNT=1 +17 7578484 COSM44099 GA G . . GENE=TP53;STRAND=-;CDS=c.445delT;AA=p.S149fs*21;CNT=1 +17 7578484 COSM1163644 GA G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.445delT;AA=p.S149fs*21;CNT=1 +17 7578484 COSM1163645 GA G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.445delT;AA=p.S149fs*21;CNT=1 +17 7578484 COSM1163647 GA G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.49delT;AA=p.S17fs*21;CNT=1 +17 7578484 COSM1163646 GA G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.166delT;AA=p.S56fs*21;CNT=1 +17 7578492 COSM131517 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.438G>A;AA=p.W146*;CNT=2 +17 7578492 COSM131519 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.159G>A;AA=p.W53*;CNT=2 +17 7578492 COSM131520 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.42G>A;AA=p.W14*;CNT=2 +17 7578492 COSM10727 C T . . GENE=TP53;STRAND=-;CDS=c.438G>A;AA=p.W146*;CNT=3 +17 7578492 COSM131518 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.438G>A;AA=p.W146*;CNT=2 +17 7578493 COSM417960 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.437G>C;AA=p.W146S;CNT=1 +17 7578493 COSM417961 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.437G>C;AA=p.W146S;CNT=1 +17 7578493 COSM43609 C T . . GENE=TP53;STRAND=-;CDS=c.437G>A;AA=p.W146*;CNT=1 +17 7578493 COSM417962 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.158G>C;AA=p.W53S;CNT=1 +17 7578493 COSM1158445 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.437G>A;AA=p.W146*;CNT=1 +17 7578493 COSM1158446 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.437G>A;AA=p.W146*;CNT=1 +17 7578493 COSM1158448 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.41G>A;AA=p.W14*;CNT=1 +17 7578493 COSM1158447 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.158G>A;AA=p.W53*;CNT=1 +17 7578493 COSM46220 C G . . GENE=TP53;STRAND=-;CDS=c.437G>C;AA=p.W146S;CNT=1 +17 7578493 COSM417963 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.41G>C;AA=p.W14S;CNT=1 +17 7578496 COSM44137 A T . . GENE=TP53;STRAND=-;CDS=c.434T>A;AA=p.L145Q;CNT=1 +17 7578496 COSM45351 A C . . GENE=TP53;STRAND=-;CDS=c.434T>G;AA=p.L145R;CNT=1 +17 7578496 COSM128671 AGCTG A . . GENE=TP53;STRAND=-;CDS=c.430_433delCAGC;AA=p.Q144fs*25;CNT=1 +17 7578496 COSM128672 AGCTG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.430_433delCAGC;AA=p.Q144fs*25;CNT=1 +17 7578496 COSM128673 AGCTG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.430_433delCAGC;AA=p.Q144fs*25;CNT=1 +17 7578496 COSM128675 AGCTG A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.34_37delCAGC;AA=p.Q12fs*25;CNT=1 +17 7578496 COSM128674 AGCTG A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.151_154delCAGC;AA=p.Q51fs*25;CNT=1 +17 7578500 COSM318147 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.34C>T;AA=p.Q12*;CNT=4 +17 7578500 COSM318146 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.430C>T;AA=p.Q144*;CNT=4 +17 7578500 COSM318148 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.151C>T;AA=p.Q51*;CNT=4 +17 7578500 COSM318145 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.430C>T;AA=p.Q144*;CNT=4 +17 7578500 COSM11245 G A . . GENE=TP53;STRAND=-;CDS=c.430C>T;AA=p.Q144*;CNT=8 +17 7578502 COSM98967 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.428T>C;AA=p.V143A;CNT=1 +17 7578502 COSM98969 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.149T>C;AA=p.V50A;CNT=1 +17 7578502 COSM179830 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.428T>C;AA=p.V143A;CNT=1 +17 7578502 COSM11306 A G . . GENE=TP53;STRAND=-;CDS=c.428T>C;AA=p.V143A;CNT=1 +17 7578502 COSM98968 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.32T>C;AA=p.V11A;CNT=1 +17 7578503 COSM220754 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.427G>A;AA=p.V143M;CNT=1 +17 7578503 COSM220753 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.427G>A;AA=p.V143M;CNT=1 +17 7578503 COSM220756 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.148G>A;AA=p.V50M;CNT=1 +17 7578503 COSM43878 C T . . GENE=TP53;STRAND=-;CDS=c.427G>A;AA=p.V143M;CNT=1 +17 7578503 COSM220755 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.31G>A;AA=p.V11M;CNT=1 +17 7578504 COSM69088 AGGGCAGG A . . GENE=TP53;STRAND=-;CDS=c.419_425delCCTGCCC;AA=p.T140fs*28;CNT=1 +17 7578504 COSM111674 AGGGCAGGTCTTGGCC A . . GENE=TP53;STRAND=-;CDS=c.411_425del15;AA=p.A138_P142delAKTCP;CNT=1 +17 7578504 COSM111678 AGGGCAGGTCTTGGCC A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.411_425del15;AA=p.A138_P142delAKTCP;CNT=1 +17 7578504 COSM111675 AGGGCAGGTCTTGGCC A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.411_425del15;AA=p.A138_P142delAKTCP;CNT=1 +17 7578504 COSM111676 AGGGCAGGTCTTGGCC A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.15_29del15;AA=p.A6_P10delAKTCP;CNT=1 +17 7578504 COSM111677 AGGGCAGGTCTTGGCC A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.132_146del15;AA=p.A45_P49delAKTCP;CNT=1 +17 7578507 COSM707867 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.27C>G;AA=p.C9W;CNT=1 +17 7578507 COSM707864 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.423C>G;AA=p.C141W;CNT=1 +17 7578507 COSM707865 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.423C>G;AA=p.C141W;CNT=1 +17 7578507 COSM44204 G C . . GENE=TP53;STRAND=-;CDS=c.423C>G;AA=p.C141W;CNT=1 +17 7578507 COSM707866 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.144C>G;AA=p.C48W;CNT=1 +17 7578508 COSM293912 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.422G>C;AA=p.C141S;CNT=1 +17 7578508 COSM131473 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.26G>A;AA=p.C9Y;CNT=5 +17 7578508 COSM293913 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.26G>C;AA=p.C9S;CNT=1 +17 7578508 COSM293911 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.422G>C;AA=p.C141S;CNT=1 +17 7578508 COSM43708 C T . . GENE=TP53;STRAND=-;CDS=c.422G>A;AA=p.C141Y;CNT=5 +17 7578508 COSM131470 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.422G>A;AA=p.C141Y;CNT=5 +17 7578508 COSM293910 C G . . GENE=TP53;STRAND=-;CDS=c.422G>C;AA=p.C141S;CNT=1 +17 7578508 COSM131472 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.143G>A;AA=p.C48Y;CNT=5 +17 7578508 COSM293914 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.143G>C;AA=p.C48S;CNT=1 +17 7578508 COSM131471 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.422G>A;AA=p.C141Y;CNT=5 +17 7578509 COSM290855 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.421T>C;AA=p.C141R;CNT=1 +17 7578509 COSM43901 A G . . GENE=TP53;STRAND=-;CDS=c.421T>C;AA=p.C141R;CNT=1 +17 7578509 COSM290856 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.25T>C;AA=p.C9R;CNT=1 +17 7578509 COSM290854 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.421T>C;AA=p.C141R;CNT=1 +17 7578509 COSM290857 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.142T>C;AA=p.C48R;CNT=1 +17 7578509 COSM69019 AG A . . GENE=TP53;STRAND=-;CDS=c.420delC;AA=p.C141fs*29;CNT=1 +17 7578509 COSM166235 AGGTCTT A . . GENE=TP53;STRAND=-;CDS=c.415_420delAAGACC;AA=p.K139_T140delKT;CNT=1 +17 7578509 COSM166237 AGGTCTT A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.415_420delAAGACC;AA=p.K139_T140delKT;CNT=1 +17 7578509 COSM166236 AGGTCTT A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.415_420delAAGACC;AA=p.K139_T140delKT;CNT=1 +17 7578509 COSM166238 AGGTCTT A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.19_24delAAGACC;AA=p.K7_T8delKT;CNT=1 +17 7578509 COSM166239 AGGTCTT A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.136_141delAAGACC;AA=p.K46_T47delKT;CNT=1 +17 7578512 COSM255062 TCTTGGCCAGTTGGC T . . GENE=TP53;STRAND=-;CDS=c.404_417del14;AA=p.C135fs*9;CNT=1 +17 7578512 COSM255064 TCTTGGCCAGTTGGC T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.404_417del14;AA=p.C135fs*9;CNT=1 +17 7578512 COSM255063 TCTTGGCCAGTTGGC T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.404_417del14;AA=p.C135fs*9;CNT=1 +17 7578512 COSM255065 TCTTGGCCAGTTGGC T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.8_21del14;AA=p.C3fs*9;CNT=1 +17 7578512 COSM255066 TCTTGGCCAGTTGGC T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.125_138del14;AA=p.C42fs*9;CNT=1 +17 7578513 COSM1158464 C CT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.416_417insA;AA=p.T140fs*9;CNT=1 +17 7578513 COSM1158463 C CT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.416_417insA;AA=p.T140fs*9;CNT=1 +17 7578513 COSM1158466 C CT . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.20_21insA;AA=p.T8fs*9;CNT=1 +17 7578513 COSM1158462 C CT . . GENE=TP53;STRAND=-;CDS=c.416_417insA;AA=p.T140fs*9;CNT=1 +17 7578513 COSM1158465 C CT . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.137_138insA;AA=p.T47fs*9;CNT=1 +17 7578515 COSM1172501 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.415A>T;AA=p.K139*;CNT=1 +17 7578515 COSM1172503 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.136A>T;AA=p.K46*;CNT=1 +17 7578515 COSM44678 T A . . GENE=TP53;STRAND=-;CDS=c.415A>T;AA=p.K139*;CNT=1 +17 7578515 COSM307285 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.415A>G;AA=p.K139E;CNT=1 +17 7578515 COSM307287 T C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.19A>G;AA=p.K7E;CNT=1 +17 7578515 COSM1172504 T A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.19A>T;AA=p.K7*;CNT=1 +17 7578515 COSM1172502 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.415A>T;AA=p.K139*;CNT=1 +17 7578515 COSM44449 T C . . GENE=TP53;STRAND=-;CDS=c.415A>G;AA=p.K139E;CNT=1 +17 7578515 COSM307288 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.136A>G;AA=p.K46E;CNT=1 +17 7578515 COSM307286 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.415A>G;AA=p.K139E;CNT=1 +17 7578515 COSM18594 TG T . . GENE=TP53;STRAND=-;CDS=c.414delC;AA=p.K139fs*31;CNT=1 +17 7578515 COSM166230 TG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.414delC;AA=p.K139fs*31;CNT=1 +17 7578515 COSM166229 TG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.414delC;AA=p.K139fs*31;CNT=1 +17 7578515 COSM166231 TG T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.18delC;AA=p.K7fs*31;CNT=1 +17 7578515 COSM166232 TG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.135delC;AA=p.K46fs*31;CNT=1 +17 7578517 COSM43818 G A . . GENE=TP53;STRAND=-;CDS=c.413C>T;AA=p.A138V;CNT=1 +17 7578517 COSM288786 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.17C>T;AA=p.A6V;CNT=1 +17 7578517 COSM288784 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.413C>T;AA=p.A138V;CNT=1 +17 7578517 COSM288785 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.413C>T;AA=p.A138V;CNT=1 +17 7578517 COSM288787 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.134C>T;AA=p.A45V;CNT=1 +17 7578518 COSM11188 C G . . GENE=TP53;STRAND=-;CDS=c.412G>C;AA=p.A138P;CNT=1 +17 7578518 COSM129861 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.412G>C;AA=p.A138P;CNT=1 +17 7578518 COSM129860 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.412G>C;AA=p.A138P;CNT=1 +17 7578518 COSM129863 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.16G>C;AA=p.A6P;CNT=1 +17 7578518 COSM129862 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.133G>C;AA=p.A45P;CNT=1 +17 7578524 COSM126985 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.406C>T;AA=p.Q136*;CNT=1 +17 7578524 COSM126987 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.127C>T;AA=p.Q43*;CNT=1 +17 7578524 COSM126986 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.406C>T;AA=p.Q136*;CNT=1 +17 7578524 COSM126988 G A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.10C>T;AA=p.Q4*;CNT=1 +17 7578524 COSM11166 G A . . GENE=TP53;STRAND=-;CDS=c.406C>T;AA=p.Q136*;CNT=2 +17 7578525 COSM437602 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.405C>G;AA=p.C135W;CNT=2 +17 7578525 COSM437601 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.405C>G;AA=p.C135W;CNT=2 +17 7578525 COSM437604 G C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.9C>G;AA=p.C3W;CNT=2 +17 7578525 COSM44219 G C . . GENE=TP53;STRAND=-;CDS=c.405C>G;AA=p.C135W;CNT=2 +17 7578525 COSM437603 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.126C>G;AA=p.C42W;CNT=2 +17 7578526 COSM303851 C A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.8G>T;AA=p.C3F;CNT=2 +17 7578526 COSM10801 C T . . GENE=TP53;STRAND=-;CDS=c.404G>A;AA=p.C135Y;CNT=3 +17 7578526 COSM44643 C G . . GENE=TP53;STRAND=-;CDS=c.404G>C;AA=p.C135S;CNT=1 +17 7578526 COSM10647 C A . . GENE=TP53;STRAND=-;CDS=c.404G>T;AA=p.C135F;CNT=2 +17 7578526 COSM300820 C G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.8G>C;AA=p.C3S;CNT=1 +17 7578526 COSM300821 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.125G>C;AA=p.C42S;CNT=1 +17 7578526 COSM303849 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.404G>T;AA=p.C135F;CNT=2 +17 7578526 COSM300819 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.404G>C;AA=p.C135S;CNT=1 +17 7578526 COSM303852 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.125G>T;AA=p.C42F;CNT=2 +17 7578526 COSM99598 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.404G>A;AA=p.C135Y;CNT=2 +17 7578526 COSM99599 C T . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.8G>A;AA=p.C3Y;CNT=2 +17 7578526 COSM99600 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.125G>A;AA=p.C42Y;CNT=2 +17 7578526 COSM99601 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.404G>A;AA=p.C135Y;CNT=2 +17 7578526 COSM300818 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.404G>C;AA=p.C135S;CNT=1 +17 7578526 COSM303850 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.404G>T;AA=p.C135F;CNT=2 +17 7578526 COSM13156 CA C . . GENE=TP53;STRAND=-;CDS=c.403delT;AA=p.C135fs*35;CNT=1 +17 7578526 COSM392225 CA C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.403delT;AA=p.C135fs*35;CNT=1 +17 7578526 COSM392226 CA C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.403delT;AA=p.C135fs*35;CNT=1 +17 7578526 COSM392228 CA C . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.7delT;AA=p.C3fs*35;CNT=1 +17 7578526 COSM392227 CA C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.124delT;AA=p.C42fs*35;CNT=1 +17 7578527 COSM308321 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.124T>C;AA=p.C42R;CNT=1 +17 7578527 COSM10684 A G . . GENE=TP53;STRAND=-;CDS=c.403T>C;AA=p.C135R;CNT=2 +17 7578527 COSM308319 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.403T>C;AA=p.C135R;CNT=1 +17 7578527 COSM308320 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.7T>C;AA=p.C3R;CNT=1 +17 7578527 COSM308318 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.403T>C;AA=p.C135R;CNT=1 +17 7578527 COSM166221 AAAAC A . . GENE=TP53;STRAND=-;CDS=c.399_402delGTTT;AA=p.M133fs*36;CNT=1 +17 7578527 COSM166223 AAAAC A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.399_402delGTTT;AA=p.M133fs*36;CNT=1 +17 7578527 COSM166222 AAAAC A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.399_402delGTTT;AA=p.M133fs*36;CNT=1 +17 7578527 COSM166224 AAAAC A . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.3_6delGTTT;AA=p.?;CNT=1 +17 7578527 COSM166225 AAAAC A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.120_123delGTTT;AA=p.M40fs*36;CNT=1 +17 7578530 COSM44654 A G . . GENE=TP53;STRAND=-;CDS=c.400T>C;AA=p.F134L;CNT=1 +17 7578530 COSM43941 A C . . GENE=TP53;STRAND=-;CDS=c.400T>G;AA=p.F134V;CNT=1 +17 7578530 COSM220775 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.400T>C;AA=p.F134L;CNT=1 +17 7578530 COSM220777 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.121T>C;AA=p.F41L;CNT=1 +17 7578530 COSM220776 A G . . GENE=TP53_ENST00000414315;STRAND=-;CDS=c.4T>C;AA=p.F2L;CNT=1 +17 7578530 COSM220774 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.400T>C;AA=p.F134L;CNT=1 +17 7578534 COSM301220 C G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.396G>C;AA=p.K132N;CNT=1 +17 7578534 COSM301222 C G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.117G>C;AA=p.K39N;CNT=1 +17 7578534 COSM10991 C A . . GENE=TP53;STRAND=-;CDS=c.396G>T;AA=p.K132N;CNT=4 +17 7578534 COSM43963 C G . . GENE=TP53;STRAND=-;CDS=c.396G>C;AA=p.K132N;CNT=1 +17 7578534 COSM213186 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.396G>T;AA=p.K132N;CNT=2 +17 7578534 COSM301221 C G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.396G>C;AA=p.K132N;CNT=1 +17 7578534 COSM213187 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.396G>T;AA=p.K132N;CNT=2 +17 7578534 COSM213188 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.117G>T;AA=p.K39N;CNT=2 +17 7578535 COSM43592 T A . . GENE=TP53;STRAND=-;CDS=c.395A>T;AA=p.K132M;CNT=1 +17 7578535 COSM308311 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.395A>G;AA=p.K132R;CNT=2 +17 7578535 COSM43912 T G . . GENE=TP53;STRAND=-;CDS=c.395A>C;AA=p.K132T;CNT=1 +17 7578535 COSM308310 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.395A>G;AA=p.K132R;CNT=2 +17 7578535 COSM179832 T G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.395A>C;AA=p.K132T;CNT=1 +17 7578535 COSM11582 T C . . GENE=TP53;STRAND=-;CDS=c.395A>G;AA=p.K132R;CNT=3 +17 7578535 COSM179831 T G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.395A>C;AA=p.K132T;CNT=1 +17 7578535 COSM308312 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.116A>G;AA=p.K39R;CNT=2 +17 7578535 COSM179833 T G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.116A>C;AA=p.K39T;CNT=1 +17 7578536 COSM10813 T C . . GENE=TP53;STRAND=-;CDS=c.394A>G;AA=p.K132E;CNT=2 +17 7578536 COSM437609 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.394A>G;AA=p.K132E;CNT=1 +17 7578536 COSM437610 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.394A>G;AA=p.K132E;CNT=1 +17 7578536 COSM437611 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.115A>G;AA=p.K39E;CNT=1 +17 7578538 COSM213374 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.392A>T;AA=p.N131I;CNT=1 +17 7578538 COSM213375 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.113A>T;AA=p.N38I;CNT=1 +17 7578538 COSM213373 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.392A>T;AA=p.N131I;CNT=1 +17 7578538 COSM44794 T A . . GENE=TP53;STRAND=-;CDS=c.392A>T;AA=p.N131I;CNT=1 +17 7578541 COSM69196 A AGG . . GENE=TP53;STRAND=-;CDS=c.388_389insCC;AA=p.L130fs*41;CNT=1 +17 7578541 COSM45499 AG A . . GENE=TP53;STRAND=-;CDS=c.388delC;AA=p.L130fs*40;CNT=1 +17 7578541 COSM404934 AGGGCAG A . . GENE=TP53;STRAND=-;CDS=c.383_388delCTGCCC;AA=p.P128_A129delPA;CNT=1 +17 7578541 COSM1167680 AG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.388delC;AA=p.L130fs*40;CNT=1 +17 7578541 COSM404935 AGGGCAG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.383_388delCTGCCC;AA=p.P128_A129delPA;CNT=1 +17 7578541 COSM1167681 AG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.388delC;AA=p.L130fs*40;CNT=1 +17 7578541 COSM404936 AGGGCAG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.383_388delCTGCCC;AA=p.P128_A129delPA;CNT=1 +17 7578541 COSM1167682 AG A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.109delC;AA=p.L37fs*40;CNT=1 +17 7578541 COSM404937 AGGGCAG A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.104_109delCTGCCC;AA=p.P35_A36delPA;CNT=1 +17 7578542 COSM11449 G A . . GENE=TP53;STRAND=-;CDS=c.388C>T;AA=p.L130F;CNT=3 +17 7578542 COSM11462 G C . . GENE=TP53;STRAND=-;CDS=c.388C>G;AA=p.L130V;CNT=1 +17 7578542 COSM247950 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.388C>T;AA=p.L130F;CNT=3 +17 7578542 COSM247952 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.109C>T;AA=p.L37F;CNT=3 +17 7578542 COSM247951 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.388C>T;AA=p.L130F;CNT=3 +17 7578544 COSM131020 GC G . . GENE=TP53;STRAND=-;CDS=c.385delG;AA=p.A129fs*41;CNT=1 +17 7578544 COSM131021 GC G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.385delG;AA=p.A129fs*41;CNT=1 +17 7578544 COSM131022 GC G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.385delG;AA=p.A129fs*41;CNT=1 +17 7578544 COSM131023 GC G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.106delG;AA=p.A36fs*41;CNT=1 +17 7578550 COSM216414 G A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.101C>T;AA=p.S34F;CNT=5 +17 7578550 COSM216413 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.380C>T;AA=p.S127F;CNT=5 +17 7578550 COSM43970 G T . . GENE=TP53;STRAND=-;CDS=c.380C>A;AA=p.S127Y;CNT=1 +17 7578550 COSM562619 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.380C>G;AA=p.S127C;CNT=2 +17 7578550 COSM562618 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.380C>G;AA=p.S127C;CNT=2 +17 7578550 COSM45483 G C . . GENE=TP53;STRAND=-;CDS=c.380C>G;AA=p.S127C;CNT=2 +17 7578550 COSM216412 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.380C>T;AA=p.S127F;CNT=5 +17 7578550 COSM44226 G A . . GENE=TP53;STRAND=-;CDS=c.380C>T;AA=p.S127F;CNT=7 +17 7578550 COSM562620 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.101C>G;AA=p.S34C;CNT=2 +17 7578550 COSM242005 G GG . . GENE=TP53;STRAND=-;CDS=c.379_380insC;AA=p.A129fs*20;CNT=1 +17 7578550 COSM242007 G GG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.379_380insC;AA=p.A129fs*20;CNT=1 +17 7578550 COSM242008 G GG . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.100_101insC;AA=p.A36fs*20;CNT=1 +17 7578550 COSM242006 G GG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.379_380insC;AA=p.A129fs*20;CNT=1 +17 7578551 COSM1168839 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.379T>A;AA=p.S127T;CNT=1 +17 7578551 COSM1168841 A T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.100T>A;AA=p.S34T;CNT=1 +17 7578551 COSM259102 A G . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.100T>C;AA=p.S34P;CNT=1 +17 7578551 COSM53285 A T . . GENE=TP53;STRAND=-;CDS=c.379T>A;AA=p.S127T;CNT=1 +17 7578551 COSM44687 A G . . GENE=TP53;STRAND=-;CDS=c.379T>C;AA=p.S127P;CNT=1 +17 7578551 COSM259101 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.379T>C;AA=p.S127P;CNT=1 +17 7578551 COSM259100 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.379T>C;AA=p.S127P;CNT=1 +17 7578551 COSM1168840 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.379T>A;AA=p.S127T;CNT=1 +17 7578552 COSM99945 G C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.99C>G;AA=p.Y33*;CNT=2 +17 7578552 COSM99946 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.378C>G;AA=p.Y126*;CNT=2 +17 7578552 COSM99944 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.378C>G;AA=p.Y126*;CNT=2 +17 7578552 COSM10862 G C . . GENE=TP53;STRAND=-;CDS=c.378C>G;AA=p.Y126*;CNT=2 +17 7578554 COSM220784 A C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.97T>G;AA=p.Y33D;CNT=3 +17 7578554 COSM220783 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.376T>G;AA=p.Y126D;CNT=3 +17 7578554 COSM220782 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.376T>G;AA=p.Y126D;CNT=3 +17 7578554 COSM43900 A C . . GENE=TP53;STRAND=-;CDS=c.376T>G;AA=p.Y126D;CNT=3 +17 7578555 COSM1167885 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.376-1G>T;AA=p.?;CNT=1 +17 7578555 COSM1167887 C A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.97-1G>T;AA=p.?;CNT=1 +17 7578555 COSM218536 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.376-1G>A;AA=p.?;CNT=4 +17 7578555 COSM6900 C T . . GENE=TP53;STRAND=-;CDS=c.376-1G>A;AA=p.?;CNT=2 +17 7578555 COSM218538 C T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.97-1G>A;AA=p.?;CNT=5 +17 7578555 COSM1167886 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.376-1G>T;AA=p.?;CNT=1 +17 7578555 COSM21572 C T . . GENE=TP53;STRAND=-;CDS=c.376-1G>A;AA=p.?;CNT=4 +17 7578555 COSM22908 C A . . GENE=TP53;STRAND=-;CDS=c.376-1G>T;AA=p.?;CNT=3 +17 7578555 COSM218537 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.376-1G>A;AA=p.?;CNT=4 +17 7578556 COSM21585 T A . . GENE=TP53;STRAND=-;CDS=c.376-2A>T;AA=p.?;CNT=2 +17 7578556 COSM45672 T C . . GENE=TP53;STRAND=-;CDS=c.376-2A>G;AA=p.?;CNT=4 +17 7578556 COSM562615 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.376-2A>T;AA=p.?;CNT=2 +17 7578556 COSM318168 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.97-2A>G;AA=p.?;CNT=2 +17 7578556 COSM562617 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.97-2A>T;AA=p.?;CNT=2 +17 7578556 COSM562616 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.376-2A>T;AA=p.?;CNT=2 +17 7578556 COSM318167 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.376-2A>G;AA=p.?;CNT=2 +17 7578556 COSM318166 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.376-2A>G;AA=p.?;CNT=2 +17 7579330 COSM122107 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.357C>A;AA=p.A119A;CNT=1 +17 7579330 COSM43668 G T . . GENE=TP53;STRAND=-;CDS=c.357C>A;AA=p.A119A;CNT=1 +17 7579330 COSM122108 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.357C>A;AA=p.A119A;CNT=1 +17 7579334 COSM318158 G GT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.352_353insA;AA=p.T118fs*31;CNT=1 +17 7579334 COSM318157 G GT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.352_353insA;AA=p.T118fs*31;CNT=1 +17 7579334 COSM318156 G GT . . GENE=TP53;STRAND=-;CDS=c.352_353insA;AA=p.T118fs*31;CNT=1 +17 7579335 COSM69197 T TC . . GENE=TP53;STRAND=-;CDS=c.351_352insG;AA=p.T118fs*31;CNT=1 +17 7579346 COSM46344 A T . . GENE=TP53;STRAND=-;CDS=c.341T>A;AA=p.L114*;CNT=2 +17 7579346 COSM331842 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.341T>A;AA=p.L114*;CNT=2 +17 7579346 COSM331841 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.341T>A;AA=p.L114*;CNT=2 +17 7579349 COSM287503 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.338T>G;AA=p.F113C;CNT=2 +17 7579349 COSM10717 A C . . GENE=TP53;STRAND=-;CDS=c.338T>G;AA=p.F113C;CNT=2 +17 7579349 COSM287502 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.338T>G;AA=p.F113C;CNT=2 +17 7579350 COSM165070 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.337T>G;AA=p.F113V;CNT=1 +17 7579350 COSM165071 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.337T>G;AA=p.F113V;CNT=1 +17 7579350 COSM11498 A C . . GENE=TP53;STRAND=-;CDS=c.337T>G;AA=p.F113V;CNT=1 +17 7579355 COSM44570 A C . . GENE=TP53;STRAND=-;CDS=c.332T>G;AA=p.L111R;CNT=2 +17 7579355 COSM707861 A T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.332T>A;AA=p.L111Q;CNT=2 +17 7579355 COSM307284 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.332T>G;AA=p.L111R;CNT=2 +17 7579355 COSM707860 A T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.332T>A;AA=p.L111Q;CNT=2 +17 7579355 COSM307283 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.332T>G;AA=p.L111R;CNT=2 +17 7579355 COSM44630 A T . . GENE=TP53;STRAND=-;CDS=c.332T>A;AA=p.L111Q;CNT=2 +17 7579358 COSM99929 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.329G>T;AA=p.R110L;CNT=5 +17 7579358 COSM10716 C A . . GENE=TP53;STRAND=-;CDS=c.329G>T;AA=p.R110L;CNT=5 +17 7579358 COSM99928 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.329G>T;AA=p.R110L;CNT=5 +17 7579358 COSM44669 CG C . . GENE=TP53;STRAND=-;CDS=c.328delC;AA=p.R110fs*13;CNT=2 +17 7579358 COSM166234 CG C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.328delC;AA=p.R110fs*13;CNT=2 +17 7579358 COSM166233 CG C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.328delC;AA=p.R110fs*13;CNT=2 +17 7579359 COSM43682 G A . . GENE=TP53;STRAND=-;CDS=c.328C>T;AA=p.R110C;CNT=1 +17 7579359 COSM247948 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.328C>T;AA=p.R110C;CNT=1 +17 7579359 COSM247949 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.328C>T;AA=p.R110C;CNT=1 +17 7579361 COSM265871 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.326T>G;AA=p.F109C;CNT=1 +17 7579361 COSM78686 A C . . GENE=TP53;STRAND=-;CDS=c.326T>G;AA=p.F109C;CNT=2 +17 7579361 COSM45169 A G . . GENE=TP53;STRAND=-;CDS=c.326T>C;AA=p.F109S;CNT=1 +17 7579361 COSM148180 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.326T>C;AA=p.F109S;CNT=1 +17 7579361 COSM265872 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.326T>G;AA=p.F109C;CNT=1 +17 7579361 COSM148181 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.326T>C;AA=p.F109S;CNT=1 +17 7579361 COSM111363 AAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGG A . . GENE=TP53;STRAND=-;CDS=c.291_325del35;AA=p.Q100fs*37;CNT=1 +17 7579361 COSM111365 AAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.291_325del35;AA=p.Q100fs*37;CNT=1 +17 7579361 COSM111364 AAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.291_325del35;AA=p.Q100fs*37;CNT=1 +17 7579362 COSM111991 A AACCGT . . GENE=TP53;STRAND=-;CDS=c.324_325insACGGT;AA=p.F109fs*16;CNT=1 +17 7579362 COSM111993 A AACCGT . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.324_325insACGGT;AA=p.F109fs*16;CNT=1 +17 7579362 COSM111992 A AACCGT . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.324_325insACGGT;AA=p.F109fs*16;CNT=1 +17 7579362 COSM13119 AACC A . . GENE=TP53;STRAND=-;CDS=c.322_324delGGT;AA=p.G108delG;CNT=3 +17 7579366 COSM213590 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.321C>A;AA=p.Y107*;CNT=2 +17 7579366 COSM45040 G T . . GENE=TP53;STRAND=-;CDS=c.321C>A;AA=p.Y107*;CNT=2 +17 7579366 COSM213589 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.321C>A;AA=p.Y107*;CNT=2 +17 7579368 COSM220765 A C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.319T>G;AA=p.Y107D;CNT=4 +17 7579368 COSM220766 A C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.319T>G;AA=p.Y107D;CNT=4 +17 7579368 COSM46103 A C . . GENE=TP53;STRAND=-;CDS=c.319T>G;AA=p.Y107D;CNT=4 +17 7579373 COSM562614 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.314G>A;AA=p.G105D;CNT=1 +17 7579373 COSM45997 C T . . GENE=TP53;STRAND=-;CDS=c.314G>A;AA=p.G105D;CNT=1 +17 7579373 COSM562613 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.314G>A;AA=p.G105D;CNT=1 +17 7579374 COSM78687 C T . . GENE=TP53;STRAND=-;CDS=c.313G>A;AA=p.G105S;CNT=1 +17 7579374 COSM338570 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.313G>T;AA=p.G105C;CNT=2 +17 7579374 COSM44481 C A . . GENE=TP53;STRAND=-;CDS=c.313G>T;AA=p.G105C;CNT=3 +17 7579374 COSM338571 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.313G>T;AA=p.G105C;CNT=2 +17 7579374 COSM45179 C G . . GENE=TP53;STRAND=-;CDS=c.313G>C;AA=p.G105R;CNT=1 +17 7579377 COSM308171 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.310C>T;AA=p.Q104*;CNT=4 +17 7579377 COSM308172 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.310C>T;AA=p.Q104*;CNT=4 +17 7579377 COSM10886 G A . . GENE=TP53;STRAND=-;CDS=c.310C>T;AA=p.Q104*;CNT=4 +17 7579378 COSM225046 G C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.309C>G;AA=p.Y103*;CNT=1 +17 7579378 COSM44453 G C . . GENE=TP53;STRAND=-;CDS=c.309C>G;AA=p.Y103*;CNT=1 +17 7579378 COSM225047 G C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.309C>G;AA=p.Y103*;CNT=1 +17 7579378 COSM707859 G T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.309C>A;AA=p.Y103*;CNT=2 +17 7579378 COSM45307 G T . . GENE=TP53;STRAND=-;CDS=c.309C>A;AA=p.Y103*;CNT=2 +17 7579378 COSM707858 G T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.309C>A;AA=p.Y103*;CNT=2 +17 7579379 COSM242009 TAGGT T . . GENE=TP53;STRAND=-;CDS=c.304_307delACCT;AA=p.Y103fs*19;CNT=1 +17 7579379 COSM255314 TAGGTTT T . . GENE=TP53;STRAND=-;CDS=c.302_307delAAACCT;AA=p.K101_Y103>N;CNT=1 +17 7579379 COSM242011 TAGGT T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.304_307delACCT;AA=p.Y103fs*19;CNT=1 +17 7579379 COSM255316 TAGGTTT T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.302_307delAAACCT;AA=p.K101_Y103>N;CNT=1 +17 7579379 COSM242010 TAGGT T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.304_307delACCT;AA=p.Y103fs*19;CNT=1 +17 7579379 COSM255315 TAGGTTT T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.302_307delAAACCT;AA=p.K101_Y103>N;CNT=1 +17 7579386 COSM323940 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.301A>T;AA=p.K101*;CNT=2 +17 7579386 COSM45259 T A . . GENE=TP53;STRAND=-;CDS=c.301A>T;AA=p.K101*;CNT=2 +17 7579386 COSM323941 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.301A>T;AA=p.K101*;CNT=2 +17 7579389 COSM1189392 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.298C>T;AA=p.Q100*;CNT=1 +17 7579389 COSM1189391 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.298C>T;AA=p.Q100*;CNT=1 +17 7579389 COSM44032 G A . . GENE=TP53;STRAND=-;CDS=c.298C>T;AA=p.Q100*;CNT=2 +17 7579389 COSM278467 GGGAA G . . GENE=TP53;STRAND=-;CDS=c.294_297delTTCC;AA=p.S99fs*23;CNT=1 +17 7579389 COSM278469 GGGAA G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.294_297delTTCC;AA=p.S99fs*23;CNT=1 +17 7579389 COSM278468 GGGAA G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.294_297delTTCC;AA=p.S99fs*23;CNT=1 +17 7579391 COSM85574 GAAGGG G . . GENE=TP53;STRAND=-;CDS=c.291_295delCCCTT;AA=p.S99fs*48;CNT=1 +17 7579391 COSM1166925 GAAGG G . . GENE=TP53;STRAND=-;CDS=c.292_295delCCTT;AA=p.S99fs*23;CNT=1 +17 7579391 COSM1166926 GAAGG G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.292_295delCCTT;AA=p.S99fs*23;CNT=1 +17 7579391 COSM1166927 GAAGG G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.292_295delCCTT;AA=p.S99fs*23;CNT=1 +17 7579396 COSM473435 G A . . GENE=TP53;STRAND=-;CDS=c.291C>T;AA=p.V97V;CNT=1 +17 7579396 COSM473436 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.291C>T;AA=p.V97V;CNT=1 +17 7579396 COSM473437 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.291C>T;AA=p.V97V;CNT=1 +17 7579409 COSM166218 AG A . . GENE=TP53;STRAND=-;CDS=c.277delC;AA=p.L93fs*30;CNT=1 +17 7579409 COSM166220 AG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.277delC;AA=p.L93fs*30;CNT=1 +17 7579409 COSM166219 AG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.277delC;AA=p.L93fs*30;CNT=1 +17 7579414 COSM44492 C T . . GENE=TP53;STRAND=-;CDS=c.273G>A;AA=p.W91*;CNT=3 +17 7579414 COSM562612 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.273G>A;AA=p.W91*;CNT=3 +17 7579414 COSM562611 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.273G>A;AA=p.W91*;CNT=3 +17 7579415 COSM323933 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.272G>A;AA=p.W91*;CNT=1 +17 7579415 COSM44192 C T . . GENE=TP53;STRAND=-;CDS=c.272G>A;AA=p.W91*;CNT=1 +17 7579415 COSM323934 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.272G>A;AA=p.W91*;CNT=1 +17 7579416 COSM242657 AGGAGGGGGCT A . . GENE=TP53;STRAND=-;CDS=c.261_270del10;AA=p.A88fs*32;CNT=1 +17 7579416 COSM242659 AGGAGGGGGCT A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.261_270del10;AA=p.A88fs*32;CNT=1 +17 7579416 COSM242658 AGGAGGGGGCT A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.261_270del10;AA=p.A88fs*32;CNT=1 +17 7579419 COSM131025 A AG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.267_268insC;AA=p.S90fs*59;CNT=1 +17 7579419 COSM131024 A AG . . GENE=TP53;STRAND=-;CDS=c.267_268insC;AA=p.S90fs*59;CNT=1 +17 7579419 COSM131026 A AG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.267_268insC;AA=p.S90fs*59;CNT=1 +17 7579419 COSM1180853 AG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.267delC;AA=p.S90fs*33;CNT=2 +17 7579419 COSM1180854 AG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.267delC;AA=p.S90fs*33;CNT=2 +17 7579422 COSM69021 GGGCTGGTGCA G . . GENE=TP53;STRAND=-;CDS=c.255_264del10;AA=p.A86fs*34;CNT=1 +17 7579423 COSM18610 GG G . . GENE=TP53;STRAND=-;CDS=c.263delC;AA=p.S90fs*33;CNT=2 +17 7579457 COSM562610 G A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.230C>T;AA=p.P77L;CNT=1 +17 7579457 COSM562608 G A . . GENE=TP53;STRAND=-;CDS=c.230C>T;AA=p.P77L;CNT=1 +17 7579457 COSM562609 G A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.230C>T;AA=p.P77L;CNT=1 +17 7579461 COSM69022 CA C . . GENE=TP53;STRAND=-;CDS=c.225delT;AA=p.A76fs*47;CNT=1 +17 7579462 COSM166226 AG A . . GENE=TP53;STRAND=-;CDS=c.224delC;AA=p.P75fs*48;CNT=1 +17 7579462 COSM166228 AG A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.224delC;AA=p.P75fs*48;CNT=1 +17 7579462 COSM166227 AG A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.224delC;AA=p.P75fs*48;CNT=1 +17 7579470 COSM128716 C CG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.216_217insC;AA=p.V73fs*76;CNT=3 +17 7579470 COSM128714 C CG . . GENE=TP53;STRAND=-;CDS=c.216_217insC;AA=p.V73fs*76;CNT=3 +17 7579470 COSM128715 C CG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.216_217insC;AA=p.V73fs*76;CNT=3 +17 7579475 COSM111573 GGA G . . GENE=TP53;STRAND=-;CDS=c.210_211delTC;AA=p.P72fs*76;CNT=1 +17 7579475 COSM111575 GGA G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.210_211delTC;AA=p.P72fs*76;CNT=1 +17 7579475 COSM111574 GGA G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.210_211delTC;AA=p.P72fs*76;CNT=1 +17 7579480 COSM707856 A G . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.207T>C;AA=p.A69A;CNT=1 +17 7579480 COSM707855 A G . . GENE=TP53;STRAND=-;CDS=c.207T>C;AA=p.A69A;CNT=1 +17 7579480 COSM707857 A G . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.207T>C;AA=p.A69A;CNT=1 +17 7579485 COSM11513 C A . . GENE=TP53;STRAND=-;CDS=c.202G>T;AA=p.E68*;CNT=1 +17 7579485 COSM131521 C A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.202G>T;AA=p.E68*;CNT=1 +17 7579485 COSM131522 C A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.202G>T;AA=p.E68*;CNT=1 +17 7579490 COSM111959 A AATTCTGGG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.196_197insCCCAGAAT;AA=p.M66fs*60;CNT=1 +17 7579490 COSM111958 A AATTCTGGG . . GENE=TP53;STRAND=-;CDS=c.196_197insCCCAGAAT;AA=p.M66fs*60;CNT=1 +17 7579490 COSM111960 A AATTCTGGG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.196_197insCCCAGAAT;AA=p.M66fs*60;CNT=1 +17 7579493 COSM218541 C CG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.193_194insC;AA=p.R65fs*84;CNT=1 +17 7579493 COSM218540 C CG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.193_194insC;AA=p.R65fs*84;CNT=1 +17 7579493 COSM218539 C CG . . GENE=TP53;STRAND=-;CDS=c.193_194insC;AA=p.R65fs*84;CNT=1 +17 7579494 COSM707853 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.193A>T;AA=p.R65*;CNT=1 +17 7579494 COSM10885 T A . . GENE=TP53;STRAND=-;CDS=c.193A>T;AA=p.R65*;CNT=2 +17 7579494 COSM707854 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.193A>T;AA=p.R65*;CNT=1 +17 7579494 COSM1159554 T TG . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.192_193insC;AA=p.R65fs*84;CNT=1 +17 7579494 COSM1159553 T TG . . GENE=TP53;STRAND=-;CDS=c.192_193insC;AA=p.R65fs*84;CNT=1 +17 7579494 COSM1159555 T TG . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.192_193insC;AA=p.R65fs*84;CNT=1 +17 7579503 COSM116689 C T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.184G>A;AA=p.E62K;CNT=1 +17 7579503 COSM116688 C T . . GENE=TP53;STRAND=-;CDS=c.184G>A;AA=p.E62K;CNT=1 +17 7579503 COSM116690 C T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.184G>A;AA=p.E62K;CNT=1 +17 7579507 COSM295960 TG T . . GENE=TP53;STRAND=-;CDS=c.179delC;AA=p.P60fs*63;CNT=1 +17 7579507 COSM295962 TG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.179delC;AA=p.P60fs*63;CNT=1 +17 7579507 COSM295961 TG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.179delC;AA=p.P60fs*63;CNT=1 +17 7579861 COSM220786 T C . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.52A>G;AA=p.T18A;CNT=1 +17 7579861 COSM220785 T C . . GENE=TP53;STRAND=-;CDS=c.52A>G;AA=p.T18A;CNT=1 +17 7579861 COSM220788 T C . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.52A>G;AA=p.T18A;CNT=1 +17 7579861 COSM220787 T C . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.52A>G;AA=p.T18A;CNT=1 +17 7579866 COSM12732 T A . . GENE=TP53;STRAND=-;CDS=c.47A>T;AA=p.Q16L;CNT=1 +17 7579866 COSM1197253 T A . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.47A>T;AA=p.Q16L;CNT=1 +17 7579866 COSM1197252 T A . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.47A>T;AA=p.Q16L;CNT=1 +17 7579866 COSM1197254 T A . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.47A>T;AA=p.Q16L;CNT=1 +17 7579866 COSM100007 TG T . . GENE=TP53;STRAND=-;CDS=c.46delC;AA=p.Q16fs*28;CNT=1 +17 7579866 COSM100010 TG T . . GENE=TP53_ENST00000269305;STRAND=-;CDS=c.46delC;AA=p.Q16fs*28;CNT=1 +17 7579866 COSM100008 TG T . . GENE=TP53_ENST00000413465;STRAND=-;CDS=c.46delC;AA=p.Q16fs*28;CNT=1 +17 7579866 COSM100009 TG T . . GENE=TP53_ENST00000545858;STRAND=-;CDS=c.46delC;AA=p.Q16fs*61;CNT=1 +17 37880219 COSM1205571 T A . . GENE=ERBB2;STRAND=+;CDS=c.2263T>A;AA=p.L755M;CNT=1 +17 37880220 COSM14060 T C . . GENE=ERBB2;STRAND=+;CDS=c.2264T>C;AA=p.L755S;CNT=2 +17 37880257 COSM51317 C G . . GENE=ERBB2;STRAND=+;CDS=c.2301C>G;AA=p.I767M;CNT=1 +17 37880981 COSM404915 A ANN . . GENE=ERBB2;STRAND=+;CDS=c.2310_2311ins12;AA=p.E770_A771insAYVM;CNT=2 +17 37881000 COSM14062 G T . . GENE=ERBB2;STRAND=+;CDS=c.2329G>T;AA=p.V777L;CNT=2 +17 37881010 COSM12555 C CGGGCTCCCC . . GENE=ERBB2;STRAND=+;CDS=c.2339_2340insGGGCTCCCC;AA=p.P780_Y781insGSP;CNT=1 +17 37881132 COSM116059 G T . . GENE=ERBB2;STRAND=+;CDS=c.2461G>T;AA=p.D821Y;CNT=1 +17 37881312 COSM213147 A T . . GENE=ERBB2;STRAND=+;CDS=c.2504A>T;AA=p.Y835F;CNT=1 +17 37881332 COSM14065 G A . . GENE=ERBB2;STRAND=+;CDS=c.2524G>A;AA=p.V842I;CNT=4 +17 37881410 COSM289684 C T . . GENE=ERBB2;STRAND=+;CDS=c.2602C>T;AA=p.R868W;CNT=1 +18 48575152 COSM84440 C T . . GENE=SMAD4;STRAND=+;CDS=c.346C>T;AA=p.Q116*;CNT=1 +18 48575159 COSM14215 C T . . GENE=SMAD4;STRAND=+;CDS=c.353C>T;AA=p.A118V;CNT=1 +18 48575172 COSM25274 A AA . . GENE=SMAD4;STRAND=+;CDS=c.366_367insA;AA=p.C123fs*2;CNT=1 +18 48575189 COSM1168851 T TA . . GENE=SMAD4;STRAND=+;CDS=c.383_384insA;AA=p.N129fs*14;CNT=1 +18 48575195 COSM218557 C T . . GENE=SMAD4;STRAND=+;CDS=c.389C>T;AA=p.P130L;CNT=1 +18 48575198 COSM84441 A G . . GENE=SMAD4;STRAND=+;CDS=c.392A>G;AA=p.Y131C;CNT=1 +18 48575200 COSM308154 C A . . GENE=SMAD4;STRAND=+;CDS=c.394C>A;AA=p.H132N;CNT=1 +18 48575206 COSM189730 G A . . GENE=SMAD4;STRAND=+;CDS=c.400G>A;AA=p.E134K;CNT=1 +18 48575209 COSM14168 C T . . GENE=SMAD4;STRAND=+;CDS=c.403C>T;AA=p.R135*;CNT=2 +18 48575213 COSM189731 T C . . GENE=SMAD4;STRAND=+;CDS=c.407T>C;AA=p.V136A;CNT=1 +18 48581229 COSM1226725 C A . . GENE=SMAD4;STRAND=+;CDS=c.533C>A;AA=p.S178*;CNT=1 +18 48581231 COSM318051 A T . . GENE=SMAD4;STRAND=+;CDS=c.535A>T;AA=p.I179F;CNT=1 +18 48581243 COSM308153 C T . . GENE=SMAD4;STRAND=+;CDS=c.547C>T;AA=p.Q183*;CNT=2 +18 48581307 COSM709388 C A . . GENE=SMAD4;STRAND=+;CDS=c.611C>A;AA=p.S204Y;CNT=1 +18 48584552 COSM563754 C G . . GENE=SMAD4;STRAND=+;CDS=c.725C>G;AA=p.S242*;CNT=1 +18 48584564 COSM1226728 C G . . GENE=SMAD4;STRAND=+;CDS=c.737C>G;AA=p.P246R;CNT=1 +18 48584569 COSM218558 C T . . GENE=SMAD4;STRAND=+;CDS=c.742C>T;AA=p.Q248*;CNT=1 +18 48584605 COSM85616 T TT . . GENE=SMAD4;STRAND=+;CDS=c.778_779insT;AA=p.Y260fs*4;CNT=2 +18 48584709 COSM87476 G T . . GENE=SMAD4;STRAND=+;CDS=c.788-1G>T;AA=p.?;CNT=1 +18 48586261 COSM164467 C G . . GENE=SMAD4;STRAND=+;CDS=c.930C>G;AA=p.F310L;CNT=1 +18 48586274 COSM438195 TC T . . GENE=SMAD4;STRAND=+;CDS=c.944delC;AA=p.N316fs*20;CNT=1 +18 48591803 COSM218559 T A . . GENE=SMAD4;STRAND=+;CDS=c.966T>A;AA=p.Y322*;CNT=1 +18 48591807 COSM189733 T C . . GENE=SMAD4;STRAND=+;CDS=c.970T>C;AA=p.C324R;CNT=1 +18 48591817 COSM189734 C T . . GENE=SMAD4;STRAND=+;CDS=c.980C>T;AA=p.A327V;CNT=1 +18 48591846 COSM417827 G A . . GENE=SMAD4;STRAND=+;CDS=c.1009G>A;AA=p.E337K;CNT=1 +18 48591865 COSM14111 C G . . GENE=SMAD4;STRAND=+;CDS=c.1028C>G;AA=p.S343*;CNT=1 +18 48591866 COSM362907 A T . . GENE=SMAD4;STRAND=+;CDS=c.1029A>T;AA=p.S343S;CNT=1 +18 48591888 COSM14135 G C . . GENE=SMAD4;STRAND=+;CDS=c.1051G>C;AA=p.D351H;CNT=1 +18 48591889 COSM373800 A G . . GENE=SMAD4;STRAND=+;CDS=c.1052A>G;AA=p.D351G;CNT=2 +18 48591901 COSM14232 A G . . GENE=SMAD4;STRAND=+;CDS=c.1064A>G;AA=p.D355G;CNT=1 +18 48591903 COSM1226726 C T . . GENE=SMAD4;STRAND=+;CDS=c.1066C>T;AA=p.P356S;CNT=1 +18 48591904 COSM14049 C T . . GENE=SMAD4;STRAND=+;CDS=c.1067C>T;AA=p.P356L;CNT=1 +18 48591904 COSM339351 C G . . GENE=SMAD4;STRAND=+;CDS=c.1067C>G;AA=p.P356R;CNT=1 +18 48591906 COSM189735 T C . . GENE=SMAD4;STRAND=+;CDS=c.1069T>C;AA=p.S357P;CNT=1 +18 48591909 COSM14174 G T . . GENE=SMAD4;STRAND=+;CDS=c.1072G>T;AA=p.G358*;CNT=1 +18 48591918 COSM14151 C A . . GENE=SMAD4;STRAND=+;CDS=c.1081C>A;AA=p.R361S;CNT=1 +18 48591918 COSM1158192 C G . . GENE=SMAD4;STRAND=+;CDS=c.1081C>G;AA=p.R361G;CNT=1 +18 48591918 COSM14140 C T . . GENE=SMAD4;STRAND=+;CDS=c.1081C>T;AA=p.R361C;CNT=5 +18 48591919 COSM14122 G A . . GENE=SMAD4;STRAND=+;CDS=c.1082G>A;AA=p.R361H;CNT=12 +18 48591965 COSM404989 TGA T . . GENE=SMAD4;STRAND=+;CDS=c.1129_1130delGA;AA=p.R378fs*14;CNT=1 +18 48591976 COSM1226732 G A . . GENE=SMAD4;STRAND=+;CDS=c.1139G>A;AA=p.R380K;CNT=1 +18 48593406 COSM1172551 G T . . GENE=SMAD4;STRAND=+;CDS=c.1157G>T;AA=p.G386V;CNT=2 +18 48593465 COSM14103 G A . . GENE=SMAD4;STRAND=+;CDS=c.1216G>A;AA=p.A406T;CNT=1 +18 48593478 COSM14223 A ACA . . GENE=SMAD4;STRAND=+;CDS=c.1229_1230insCA;AA=p.Q410fs*6;CNT=1 +18 48593490 COSM1158549 T TAA . . GENE=SMAD4;STRAND=+;CDS=c.1241_1242insAA;AA=p.D415fs*22;CNT=1 +18 48593498 COSM1158504 G T . . GENE=SMAD4;STRAND=+;CDS=c.1249G>T;AA=p.E417*;CNT=1 +18 48593532 COSM308152 A G . . GENE=SMAD4;STRAND=+;CDS=c.1283A>G;AA=p.K428R;CNT=1 +18 48593541 COSM218560 CA C . . GENE=SMAD4;STRAND=+;CDS=c.1293delA;AA=p.S432fs*4;CNT=1 +18 48603009 COSM265853 T A . . GENE=SMAD4;STRAND=+;CDS=c.1310T>A;AA=p.V437D;CNT=1 +18 48603032 COSM14096 C T . . GENE=SMAD4;STRAND=+;CDS=c.1333C>T;AA=p.R445*;CNT=2 +18 48603145 COSM308194 CAGTA C . . GENE=SMAD4;STRAND=+;CDS=c.1447_1447+3delAgta;AA=p.?;CNT=1 +18 48604652 COSM14222 G T . . GENE=SMAD4;STRAND=+;CDS=c.1474G>T;AA=p.V492F;CNT=1 +18 48604655 COSM14227 G A . . GENE=SMAD4;STRAND=+;CDS=c.1477G>A;AA=p.D493N;CNT=1 +18 48604656 COSM14171 A C . . GENE=SMAD4;STRAND=+;CDS=c.1478A>C;AA=p.D493A;CNT=1 +18 48604659 COSM84443 A G . . GENE=SMAD4;STRAND=+;CDS=c.1481A>G;AA=p.D494G;CNT=1 +18 48604665 COSM14193 G A . . GENE=SMAD4;STRAND=+;CDS=c.1487G>A;AA=p.R496H;CNT=1 +18 48604686 COSM85640 T TT . . GENE=SMAD4;STRAND=+;CDS=c.1508_1509insT;AA=p.M503fs*24;CNT=1 +18 48604690 COSM14148 T A . . GENE=SMAD4;STRAND=+;CDS=c.1512T>A;AA=p.S504R;CNT=1 +18 48604692 COSM1226727 T A . . GENE=SMAD4;STRAND=+;CDS=c.1514T>A;AA=p.F505Y;CNT=1 +18 48604704 COSM241693 G A . . GENE=SMAD4;STRAND=+;CDS=c.1526G>A;AA=p.W509*;CNT=1 +18 48604705 COSM35631 G A . . GENE=SMAD4;STRAND=+;CDS=c.1527G>A;AA=p.W509*;CNT=1 +18 48604706 COSM189742 G A . . GENE=SMAD4;STRAND=+;CDS=c.1528G>A;AA=p.G510R;CNT=1 +18 48604717 COSM299787 C G . . GENE=SMAD4;STRAND=+;CDS=c.1539C>G;AA=p.Y513*;CNT=1 +18 48604725 COSM85570 AGAGCATCA A . . GENE=SMAD4;STRAND=+;CDS=c.1548_1555delGAGCATCA;AA=p.S517fs*7;CNT=1 +18 48604736 COSM189743 G T . . GENE=SMAD4;STRAND=+;CDS=c.1558G>T;AA=p.E520*;CNT=1 +18 48604749 COSM1226729 G C . . GENE=SMAD4;STRAND=+;CDS=c.1571G>C;AA=p.W524S;CNT=1 +18 48604750 COSM218561 G C . . GENE=SMAD4;STRAND=+;CDS=c.1572G>C;AA=p.W524C;CNT=1 +18 48604754 COSM14134 G T . . GENE=SMAD4;STRAND=+;CDS=c.1576G>T;AA=p.E526*;CNT=1 +18 48604755 COSM218562 A T . . GENE=SMAD4;STRAND=+;CDS=c.1577A>T;AA=p.E526V;CNT=1 +18 48604776 COSM189744 T G . . GENE=SMAD4;STRAND=+;CDS=c.1598T>G;AA=p.L533R;CNT=1 +18 48604776 COSM1168852 T TCAG . . GENE=SMAD4;STRAND=+;CDS=c.1598_1599insCAG;AA=p.L533_Q534insS;CNT=1 +18 48604777 COSM85571 CC C . . GENE=SMAD4;STRAND=+;CDS=c.1600delC;AA=p.Q534fs*3;CNT=1 +18 48604785 COSM218563 T A . . GENE=SMAD4;STRAND=+;CDS=c.1607T>A;AA=p.L536Q;CNT=1 +18 48604785 COSM1168853 TAGACGA T . . GENE=SMAD4;STRAND=+;CDS=c.1608_1613delAGACGA;AA=p.D537_E538delDE;CNT=1 +18 48604787 COSM14164 G T . . GENE=SMAD4;STRAND=+;CDS=c.1609G>T;AA=p.D537Y;CNT=1 +18 48604788 COSM256174 A T . . GENE=SMAD4;STRAND=+;CDS=c.1610A>T;AA=p.D537V;CNT=1 +18 48604788 COSM168813 A G . . GENE=SMAD4;STRAND=+;CDS=c.1610A>G;AA=p.D537G;CNT=1 +18 48604789 COSM709386 C A . . GENE=SMAD4;STRAND=+;CDS=c.1611C>A;AA=p.D537E;CNT=1 +18 48604797 COSM14165 T G . . GENE=SMAD4;STRAND=+;CDS=c.1619T>G;AA=p.L540R;CNT=1 +18 48604799 COSM247457 C T . . GENE=SMAD4;STRAND=+;CDS=c.1621C>T;AA=p.H541Y;CNT=1 +19 1207009 COSM95668 G T . . GENE=STK11;STRAND=+;CDS=c.97G>T;AA=p.E33*;CNT=1 +19 1207064 COSM391251 T TN . . GENE=STK11;STRAND=+;CDS=c.152_153insG;AA=p.D53fs*110;CNT=1 +19 1207064 COSM27282 TG T . . GENE=STK11;STRAND=+;CDS=c.153delG;AA=p.D53fs*11;CNT=1 +19 1207076 COSM392566 TG T . . GENE=STK11;STRAND=+;CDS=c.165delG;AA=p.E57fs*7;CNT=1 +19 1207078 COSM48784 G T . . GENE=STK11;STRAND=+;CDS=c.166G>T;AA=p.G56W;CNT=1 +19 1207079 COSM166199 G GTTCC . . GENE=STK11;STRAND=+;CDS=c.167_168insTTCC;AA=p.E57fs*107;CNT=1 +19 1207092 COSM405206 CG C . . GENE=STK11;STRAND=+;CDS=c.181delG;AA=p.G61fs*3;CNT=1 +19 1207096 COSM382838 A T . . GENE=STK11;STRAND=+;CDS=c.184A>T;AA=p.K62*;CNT=1 +19 1207120 COSM25846 G T . . GENE=STK11;STRAND=+;CDS=c.208G>T;AA=p.E70*;CNT=2 +19 1220487 COSM20944 G T . . GENE=STK11;STRAND=+;CDS=c.580G>T;AA=p.D194Y;CNT=2 +19 1220502 COSM25229 G T . . GENE=STK11;STRAND=+;CDS=c.595G>T;AA=p.E199*;CNT=1 +19 1220629 COSM25844 C T . . GENE=STK11;STRAND=+;CDS=c.647C>T;AA=p.S216F;CNT=1 +19 1220636 COSM377894 T C . . GENE=STK11;STRAND=+;CDS=c.654T>C;AA=p.A218A;CNT=1 +19 1221241 COSM374278 TCG TTT . . GENE=STK11;STRAND=+;CDS=c.765_766CG>TT;AA=p.F255>?;CNT=1 +19 1221270 COSM371077 G T . . GENE=STK11;STRAND=+;CDS=c.793G>T;AA=p.E265*;CNT=1 +19 1221278 COSM392578 CG C . . GENE=STK11;STRAND=+;CDS=c.802delG;AA=p.K269fs*18;CNT=1 +19 1221293 COSM29005 C T . . GENE=STK11;STRAND=+;CDS=c.816C>T;AA=p.Y272Y;CNT=1 +19 1221336 COSM332311 A T . . GENE=STK11;STRAND=+;CDS=c.859A>T;AA=p.K287*;CNT=1 +19 3114956 COSM1208385 T G . . GENE=GNA11;STRAND=+;CDS=c.491T>G;AA=p.V164G;CNT=1 +19 3118941 COSM238583 C A . . GENE=GNA11;STRAND=+;CDS=c.625C>A;AA=p.Q209K;CNT=1 +19 3118942 COSM52969 A T . . GENE=GNA11;STRAND=+;CDS=c.626A>T;AA=p.Q209L;CNT=1 +19 3121039 COSM298454 G C . . GENE=GNA11;STRAND=+;CDS=c.942G>C;AA=p.V314V;CNT=1 +19 3121127 COSM994458 G A . . GENE=GNA11;STRAND=+;CDS=c.1030G>A;AA=p.V344M;CNT=1 +19 17945701 COSM182101 C T . . GENE=JAK3;STRAND=-;CDS=c.2159G>A;AA=p.S720N;CNT=1 +19 17945718 COSM182102 C T . . GENE=JAK3;STRAND=-;CDS=c.2142G>A;AA=p.T714T;CNT=1 +19 17945731 COSM389276 C A . . GENE=JAK3;STRAND=-;CDS=c.2129G>T;AA=p.G710V;CNT=1 +19 17945734 COSM389277 C A . . GENE=JAK3;STRAND=-;CDS=c.2126G>T;AA=p.W709L;CNT=1 +19 17945801 COSM1148108 T C . . GENE=JAK3_ENST00000458235;STRAND=-;CDS=c.2059A>G;AA=p.R687G;CNT=1 +19 17945801 COSM711177 T C . . GENE=JAK3;STRAND=-;CDS=c.2059A>G;AA=p.R687G;CNT=1 +19 17947985 COSM182104 G A . . GENE=JAK3;STRAND=-;CDS=c.1739C>T;AA=p.S580L;CNT=1 +19 17948006 COSM34215 G A . . GENE=JAK3;STRAND=-;CDS=c.1718C>T;AA=p.A573V;CNT=1 +2 29432652 COSM1020008 C A . . GENE=ALK;STRAND=-;CDS=c.3836G>T;AA=p.R1279M;CNT=1 +2 29432664 COSM28056 C T . . GENE=ALK;STRAND=-;CDS=c.3824G>A;AA=p.R1275Q;CNT=3 +2 29432669 COSM442799 CATCCCG C . . GENE=ALK;STRAND=-;CDS=c.3813_3818delCGGGAT;AA=p.F1271_M1273>L;CNT=1 +2 29432731 COSM1020010 T C . . GENE=ALK;STRAND=-;CDS=c.3757A>G;AA=p.R1253G;CNT=1 +2 29443697 COSM28054 A C . . GENE=ALK;STRAND=-;CDS=c.3520T>G;AA=p.F1174V;CNT=1 +2 29443698 COSM291452 T C . . GENE=ALK;STRAND=-;CDS=c.3519A>G;AA=p.K1173K;CNT=1 +2 209113112 COSM28746 C T . . GENE=IDH1;STRAND=-;CDS=c.395G>A;AA=p.R132H;CNT=31 +2 209113113 COSM28749 G C . . GENE=IDH1;STRAND=-;CDS=c.394C>G;AA=p.R132G;CNT=2 +2 209113113 COSM28748 G T . . GENE=IDH1;STRAND=-;CDS=c.394C>A;AA=p.R132S;CNT=2 +2 209113113 COSM28747 G A . . GENE=IDH1;STRAND=-;CDS=c.394C>T;AA=p.R132C;CNT=9 +2 209113151 COSM242544 C T . . GENE=IDH1;STRAND=-;CDS=c.356G>A;AA=p.R119Q;CNT=1 +2 209113181 COSM573095 C T . . GENE=IDH1;STRAND=-;CDS=c.326G>A;AA=p.R109K;CNT=1 +2 209113233 COSM1015580 A G . . GENE=IDH1;STRAND=-;CDS=c.274T>C;AA=p.W92R;CNT=1 +2 212288914 COSM573413 G T . . GENE=ERBB4;STRAND=-;CDS=c.2832C>A;AA=p.I944I;CNT=1 +2 212288940 COSM108015 C T . . GENE=ERBB4;STRAND=-;CDS=c.2806G>A;AA=p.G936R;CNT=1 +2 212288946 COSM270830 C T . . GENE=ERBB4;STRAND=-;CDS=c.2800G>A;AA=p.E934K;CNT=1 +2 212288964 COSM169572 C A . . GENE=ERBB4;STRAND=-;CDS=c.2782G>T;AA=p.E928*;CNT=1 +2 212288968 COSM1165236 C T . . GENE=ERBB4;STRAND=-;CDS=c.2778G>A;AA=p.T926T;CNT=1 +2 212288980 COSM573412 A T . . GENE=ERBB4;STRAND=-;CDS=c.2766T>A;AA=p.D922E;CNT=1 +2 212289002 COSM1015908 G C . . GENE=ERBB4;STRAND=-;CDS=c.2744C>G;AA=p.T915S;CNT=1 +2 212530063 COSM138342 G A . . GENE=ERBB4;STRAND=-;CDS=c.1856C>T;AA=p.P619L;CNT=1 +2 212530084 COSM232263 C T . . GENE=ERBB4;STRAND=-;CDS=c.1835G>A;AA=p.R612Q;CNT=1 +2 212530091 COSM573362 G T . . GENE=ERBB4;STRAND=-;CDS=c.1828C>A;AA=p.P610T;CNT=1 +2 212530126 COSM320161 T A . . GENE=ERBB4;STRAND=-;CDS=c.1793A>T;AA=p.Q598L;CNT=1 +2 212530171 COSM170797 A T . . GENE=ERBB4;STRAND=-;CDS=c.1748T>A;AA=p.F583Y;CNT=1 +2 212530179 COSM418876 G T . . GENE=ERBB4;STRAND=-;CDS=c.1740C>A;AA=p.C580*;CNT=1 +2 212530179 COSM1015978 G A . . GENE=ERBB4;STRAND=-;CDS=c.1740C>T;AA=p.C580C;CNT=1 +2 212530205 COSM573361 G A . . GENE=ERBB4;STRAND=-;CDS=c.1717-3C>T;AA=p.?;CNT=1 +2 212576841 COSM476867 A T . . GENE=ERBB4;STRAND=-;CDS=c.1058T>A;AA=p.I353N;CNT=1 +2 212576877 COSM110095 G A . . GENE=ERBB4;STRAND=-;CDS=c.1022C>T;AA=p.S341L;CNT=1 +2 212576881 COSM353101 C A . . GENE=ERBB4;STRAND=-;CDS=c.1018G>T;AA=p.G340*;CNT=1 +2 212576896 COSM573356 C A . . GENE=ERBB4;STRAND=-;CDS=c.1003G>T;AA=p.D335Y;CNT=1 +2 212578346 COSM573355 C A . . GENE=ERBB4;STRAND=-;CDS=c.911G>T;AA=p.C304F;CNT=2 +2 212578349 COSM1015992 G A . . GENE=ERBB4;STRAND=-;CDS=c.908C>T;AA=p.S303F;CNT=1 +2 212578372 COSM160825 A C . . GENE=ERBB4;STRAND=-;CDS=c.885T>G;AA=p.H295Q;CNT=1 +2 212587123 COSM476868 C A . . GENE=ERBB4;STRAND=-;CDS=c.878G>T;AA=p.C293F;CNT=1 +2 212587172 COSM1015994 G T . . GENE=ERBB4;STRAND=-;CDS=c.829C>A;AA=p.H277N;CNT=1 +2 212587198 COSM209862 T C . . GENE=ERBB4;STRAND=-;CDS=c.803A>G;AA=p.Y268C;CNT=1 +2 212587266 COSM573354 C T . . GENE=ERBB4;STRAND=-;CDS=c.742-7G>A;AA=p.?;CNT=1 +2 212589795 COSM280847 A G . . GENE=ERBB4;STRAND=-;CDS=c.741+6T>C;AA=p.?;CNT=1 +2 212589838 COSM573353 G A . . GENE=ERBB4;STRAND=-;CDS=c.704C>T;AA=p.A235V;CNT=1 +2 212589896 COSM1178899 G A . . GENE=ERBB4;STRAND=-;CDS=c.646C>T;AA=p.Q216*;CNT=1 +2 212589909 COSM1015997 C T . . GENE=ERBB4;STRAND=-;CDS=c.633G>A;AA=p.T211T;CNT=1 +2 212652768 COSM719372 T C . . GENE=ERBB4;STRAND=-;CDS=c.538A>G;AA=p.T180A;CNT=1 +2 212652804 COSM232262 G A . . GENE=ERBB4;STRAND=-;CDS=c.502C>T;AA=p.R168W;CNT=2 +2 212652809 COSM301362 A T . . GENE=ERBB4;STRAND=-;CDS=c.497T>A;AA=p.I166N;CNT=1 +2 212652840 COSM229461 A G . . GENE=ERBB4;STRAND=-;CDS=c.466T>C;AA=p.C156R;CNT=1 +2 212812187 COSM719371 C T . . GENE=ERBB4;STRAND=-;CDS=c.389G>A;AA=p.G130E;CNT=1 +2 212812224 COSM573350 C A . . GENE=ERBB4;STRAND=-;CDS=c.352G>T;AA=p.A118S;CNT=1 +2 212812227 COSM209863 A G . . GENE=ERBB4;STRAND=-;CDS=c.349T>C;AA=p.L117L;CNT=1 +2 212812236 COSM229699 G A . . GENE=ERBB4;STRAND=-;CDS=c.340C>T;AA=p.R114*;CNT=1 +2 212812260 COSM1205582 G A . . GENE=ERBB4;STRAND=-;CDS=c.316C>T;AA=p.R106C;CNT=1 +2 212812268 COSM573349 C A . . GENE=ERBB4;STRAND=-;CDS=c.308G>T;AA=p.R103L;CNT=1 +2 212812269 COSM719370 G A . . GENE=ERBB4;STRAND=-;CDS=c.307C>T;AA=p.R103C;CNT=1 +2 212812308 COSM394748 C T . . GENE=ERBB4;STRAND=-;CDS=c.268G>A;AA=p.A90T;CNT=1 +2 212812310 COSM394749 A G . . GENE=ERBB4;STRAND=-;CDS=c.266T>C;AA=p.V89A;CNT=1 +20 57484420 COSM123397 C T . . GENE=GNAS_ENST00000371100;STRAND=+;CDS=c.2530C>T;AA=p.R844C;CNT=12 +20 57484420 COSM27887 C T . . GENE=GNAS;STRAND=+;CDS=c.601C>T;AA=p.R201C;CNT=11 +20 57484421 COSM94388 G A . . GENE=GNAS_ENST00000371100;STRAND=+;CDS=c.2531G>A;AA=p.R844H;CNT=5 +20 57484421 COSM27895 G A . . GENE=GNAS;STRAND=+;CDS=c.602G>A;AA=p.R201H;CNT=5 +20 57484436 COSM1028498 G C . . GENE=GNAS;STRAND=+;CDS=c.617G>C;AA=p.G206A;CNT=1 +20 57484436 COSM1028497 G C . . GENE=GNAS_ENST00000371100;STRAND=+;CDS=c.2546G>C;AA=p.G849A;CNT=1 +22 24133958 COSM579671 C A . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.109C>A;AA=p.R37S;CNT=1 +22 24133958 COSM579670 C A . . GENE=SMARCB1;STRAND=+;CDS=c.109C>A;AA=p.R37S;CNT=1 +22 24133963 COSM300998 GTTC G . . GENE=SMARCB1;STRAND=+;CDS=c.115_117delTTC;AA=p.F39delF;CNT=1 +22 24133967 COSM1002 C T . . GENE=SMARCB1;STRAND=+;CDS=c.118C>T;AA=p.R40*;CNT=2 +22 24134006 COSM24595 C T . . GENE=SMARCB1;STRAND=+;CDS=c.157C>T;AA=p.R53*;CNT=1 +22 24134046 COSM255201 C CA . . GENE=SMARCB1;STRAND=+;CDS=c.197_198insA;AA=p.S67fs*4;CNT=1 +22 24143214 COSM726164 C A . . GENE=SMARCB1;STRAND=+;CDS=c.446C>A;AA=p.T149K;CNT=1 +22 24143214 COSM726165 C A . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.419C>A;AA=p.T140K;CNT=1 +22 24143232 COSM1032622 G A . . GENE=SMARCB1;STRAND=+;CDS=c.464G>A;AA=p.R155H;CNT=1 +22 24143232 COSM1032623 G A . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.437G>A;AA=p.R146H;CNT=1 +22 24143240 COSM992 C T . . GENE=SMARCB1;STRAND=+;CDS=c.472C>T;AA=p.R158*;CNT=1 +22 24145583 COSM217231 G T . . GENE=SMARCB1;STRAND=+;CDS=c.602G>T;AA=p.R201L;CNT=2 +22 24145587 COSM1130489 C A . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.633C>A;AA=p.D211E;CNT=1 +22 24145587 COSM1130488 C A . . GENE=SMARCB1;STRAND=+;CDS=c.606C>A;AA=p.D202E;CNT=1 +22 24145599 COSM994 G A . . GENE=SMARCB1;STRAND=+;CDS=c.618G>A;AA=p.W206*;CNT=1 +22 24176329 COSM1226779 C T . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.1147C>T;AA=p.R383W;CNT=1 +22 24176329 COSM1226778 C T . . GENE=SMARCB1;STRAND=+;CDS=c.1120C>T;AA=p.R374W;CNT=1 +22 24176335 COSM1161418 A G . . GENE=SMARCB1_ENST00000344921;STRAND=+;CDS=c.1153A>G;AA=p.R385G;CNT=1 +22 24176335 COSM1161417 A G . . GENE=SMARCB1;STRAND=+;CDS=c.1126A>G;AA=p.R376G;CNT=1 +22 24176353 COSM29495 GC G . . GENE=SMARCB1;STRAND=+;CDS=c.1145delC;AA=p.P383fs*4;CNT=2 +3 10183771 COSM34029 T G . . GENE=VHL;STRAND=+;CDS=c.240T>G;AA=p.S80R;CNT=1 +3 10183776 COSM14382 G C . . GENE=VHL;STRAND=+;CDS=c.245G>C;AA=p.R82P;CNT=1 +3 10183788 COSM18028 C T . . GENE=VHL;STRAND=+;CDS=c.257C>T;AA=p.P86L;CNT=1 +3 10183794 COSM18351 G T . . GENE=VHL;STRAND=+;CDS=c.263G>T;AA=p.W88L;CNT=1 +3 10183794 COSM18070 G A . . GENE=VHL;STRAND=+;CDS=c.263G>A;AA=p.W88*;CNT=2 +3 10183797 COSM14346 T C . . GENE=VHL;STRAND=+;CDS=c.266T>C;AA=p.L89P;CNT=1 +3 10183848 COSM18082 G A . . GENE=VHL;STRAND=+;CDS=c.317G>A;AA=p.G106D;CNT=1 +3 10183863 COSM26151 G A . . GENE=VHL;STRAND=+;CDS=c.332G>A;AA=p.S111N;CNT=1 +3 10183867 COSM30227 C A . . GENE=VHL;STRAND=+;CDS=c.336C>A;AA=p.Y112*;CNT=1 +3 10183872 COSM30229 G A . . GENE=VHL;STRAND=+;CDS=c.340+1G>A;AA=p.?;CNT=1 +3 10183872 COSM479170 G C . . GENE=VHL;STRAND=+;CDS=c.340+1G>C;AA=p.?;CNT=1 +3 10188218 COSM34019 G T . . GENE=VHL;STRAND=+;CDS=c.361G>T;AA=p.D121Y;CNT=3 +3 10188224 COSM580792 G T . . GENE=VHL;STRAND=+;CDS=c.367G>T;AA=p.G123W;CNT=1 +3 10188237 COSM1232268 G T . . GENE=VHL;STRAND=+;CDS=c.380G>T;AA=p.G127V;CNT=1 +3 10188240 COSM17756 T A . . GENE=VHL;STRAND=+;CDS=c.383T>A;AA=p.L128H;CNT=4 +3 10188245 COSM14407 G C . . GENE=VHL;STRAND=+;CDS=c.388G>C;AA=p.V130L;CNT=1 +3 10188245 COSM97148 G T . . GENE=VHL;STRAND=+;CDS=c.388G>T;AA=p.V130F;CNT=1 +3 10188246 COSM14323 T A . . GENE=VHL;STRAND=+;CDS=c.389T>A;AA=p.V130D;CNT=1 +3 10188248 COSM17758 A T . . GENE=VHL;STRAND=+;CDS=c.391A>T;AA=p.N131Y;CNT=1 +3 10188254 COSM479174 A C . . GENE=VHL;STRAND=+;CDS=c.397A>C;AA=p.T133P;CNT=1 +3 10188257 COSM308465 GAATT G . . GENE=VHL;STRAND=+;CDS=c.401_404delAATT;AA=p.E134fs*24;CNT=1 +3 10188263 COSM18276 T G . . GENE=VHL;STRAND=+;CDS=c.406T>G;AA=p.F136V;CNT=1 +3 10188270 COSM307757 CATCTCTCA C . . GENE=VHL;STRAND=+;CDS=c.414_421delATCTCTCA;AA=p.S139fs*2;CNT=2 +3 10188287 COSM1035874 G A . . GENE=VHL;STRAND=+;CDS=c.430G>A;AA=p.G144R;CNT=1 +3 10188290 COSM97150 C T . . GENE=VHL;STRAND=+;CDS=c.433C>T;AA=p.Q145*;CNT=2 +3 10188307 COSM479175 TAT TTA . . GENE=VHL;STRAND=+;CDS=c.451_452AT>TA;AA=p.I151>?;CNT=1 +3 10188308 COSM17978 A T . . GENE=VHL;STRAND=+;CDS=c.451A>T;AA=p.I151F;CNT=1 +3 10188309 COSM17934 T C . . GENE=VHL;STRAND=+;CDS=c.452T>C;AA=p.I151T;CNT=2 +3 10188309 COSM18274 T A . . GENE=VHL;STRAND=+;CDS=c.452T>A;AA=p.I151N;CNT=1 +3 10188315 COSM14363 T C . . GENE=VHL;STRAND=+;CDS=c.458T>C;AA=p.L153P;CNT=1 +3 10188319 COSM17907 AG A . . GENE=VHL;STRAND=+;CDS=c.463delG;AA=p.V155fs*4;CNT=1 +3 10188320 COSM18152 G A . . GENE=VHL;STRAND=+;CDS=c.463G>A;AA=p.V155M;CNT=1 +3 10188321 COSM26152 G C . . GENE=VHL;STRAND=+;CDS=c.463+1G>C;AA=p.?;CNT=1 +3 10188321 COSM17989 G T . . GENE=VHL;STRAND=+;CDS=c.463+1G>T;AA=p.?;CNT=2 +3 10188322 COSM28287 T C . . GENE=VHL;STRAND=+;CDS=c.463+2T>C;AA=p.?;CNT=1 +3 10191469 COSM18054 A G . . GENE=VHL;STRAND=+;CDS=c.464-2A>G;AA=p.?;CNT=3 +3 10191470 COSM14376 G A . . GENE=VHL;STRAND=+;CDS=c.464-1G>A;AA=p.?;CNT=1 +3 10191470 COSM25675 G T . . GENE=VHL;STRAND=+;CDS=c.464-1G>T;AA=p.?;CNT=1 +3 10191470 COSM14437 G C . . GENE=VHL;STRAND=+;CDS=c.464-1G>C;AA=p.?;CNT=1 +3 10191475 COSM479176 T A . . GENE=VHL;STRAND=+;CDS=c.468T>A;AA=p.Y156*;CNT=1 +3 10191479 COSM17657 C G . . GENE=VHL;STRAND=+;CDS=c.472C>G;AA=p.L158V;CNT=3 +3 10191479 COSM479177 CTG CCC . . GENE=VHL;STRAND=+;CDS=c.473_474TG>CC;AA=p.L158>?;CNT=1 +3 10191480 COSM14387 T C . . GENE=VHL;STRAND=+;CDS=c.473T>C;AA=p.L158P;CNT=2 +3 10191481 COSM479178 G C . . GENE=VHL;STRAND=+;CDS=c.474G>C;AA=p.L158L;CNT=1 +3 10191482 COSM422840 A T . . GENE=VHL;STRAND=+;CDS=c.475A>T;AA=p.K159*;CNT=1 +3 10191485 COSM18075 G T . . GENE=VHL;STRAND=+;CDS=c.478G>T;AA=p.E160*;CNT=2 +3 10191488 COSM17612 C T . . GENE=VHL;STRAND=+;CDS=c.481C>T;AA=p.R161*;CNT=1 +3 10191489 COSM17909 G C . . GENE=VHL;STRAND=+;CDS=c.482G>C;AA=p.R161P;CNT=1 +3 10191491 COSM18073 T C . . GENE=VHL;STRAND=+;CDS=c.484T>C;AA=p.C162R;CNT=1 +3 10191492 COSM25676 G T . . GENE=VHL;STRAND=+;CDS=c.485G>T;AA=p.C162F;CNT=1 +3 10191492 COSM14408 G A . . GENE=VHL;STRAND=+;CDS=c.485G>A;AA=p.C162Y;CNT=1 +3 10191493 COSM18023 C G . . GENE=VHL;STRAND=+;CDS=c.486C>G;AA=p.C162W;CNT=1 +3 10191497 COSM17911 CAG C . . GENE=VHL;STRAND=+;CDS=c.491_492delAG;AA=p.Q164fs*9;CNT=1 +3 10191501 COSM17785 T A . . GENE=VHL;STRAND=+;CDS=c.494T>A;AA=p.V165D;CNT=1 +3 10191506 COSM14311 C T . . GENE=VHL;STRAND=+;CDS=c.499C>T;AA=p.R167W;CNT=1 +3 10191512 COSM34003 CT C . . GENE=VHL;STRAND=+;CDS=c.506delT;AA=p.L169fs*33;CNT=1 +3 10191513 COSM17837 T C . . GENE=VHL;STRAND=+;CDS=c.506T>C;AA=p.L169P;CNT=3 +3 10191524 COSM97152 G T . . GENE=VHL;STRAND=+;CDS=c.517G>T;AA=p.E173*;CNT=1 +3 10191531 COSM307756 ACAGGAGACT A . . GENE=VHL;STRAND=+;CDS=c.525_533delCAGGAGACT;AA=p.Y175_L178>*;CNT=1 +3 10191532 COSM17789 C A . . GENE=VHL;STRAND=+;CDS=c.525C>A;AA=p.Y175*;CNT=1 +3 10191533 COSM52030 AG A . . GENE=VHL;STRAND=+;CDS=c.527delG;AA=p.R176fs*25;CNT=1 +3 10191536 COSM17866 A T . . GENE=VHL;STRAND=+;CDS=c.529A>T;AA=p.R177*;CNT=1 +3 10191556 COSM727510 G A . . GENE=VHL;STRAND=+;CDS=c.549G>A;AA=p.S183S;CNT=1 +3 10191558 COSM17854 T C . . GENE=VHL;STRAND=+;CDS=c.551T>C;AA=p.L184P;CNT=2 +3 10191563 COSM168255 G A . . GENE=VHL;STRAND=+;CDS=c.556G>A;AA=p.E186K;CNT=1 +3 10191563 COSM25670 G T . . GENE=VHL;STRAND=+;CDS=c.556G>T;AA=p.E186*;CNT=1 +3 10191570 COSM25680 T G . . GENE=VHL;STRAND=+;CDS=c.563T>G;AA=p.L188R;CNT=1 +3 10191570 COSM25678 T C . . GENE=VHL;STRAND=+;CDS=c.563T>C;AA=p.L188P;CNT=2 +3 10191570 COSM479180 TGG TTT . . GENE=VHL;STRAND=+;CDS=c.564_565GG>TT;AA=p.L188>?;CNT=1 +3 10191571 COSM479179 G T . . GENE=VHL;STRAND=+;CDS=c.564G>T;AA=p.L188L;CNT=1 +3 10191572 COSM97154 G T . . GENE=VHL;STRAND=+;CDS=c.565G>T;AA=p.E189*;CNT=2 +3 10191590 COSM14359 C T . . GENE=VHL;STRAND=+;CDS=c.583C>T;AA=p.Q195*;CNT=1 +3 10191593 COSM30293 A T . . GENE=VHL;STRAND=+;CDS=c.586A>T;AA=p.K196*;CNT=1 +3 10191609 COSM1232271 T C . . GENE=VHL;STRAND=+;CDS=c.602T>C;AA=p.L201P;CNT=1 +3 10191621 COSM1232270 G A . . GENE=VHL;STRAND=+;CDS=c.614G>A;AA=p.R205H;CNT=1 +3 37067230 COSM583373 C A . . GENE=MLH1;STRAND=+;CDS=c.1141C>A;AA=p.H381N;CNT=1 +3 41266068 COSM238574 T G . . GENE=CTNNB1;STRAND=+;CDS=c.65T>G;AA=p.V22G;CNT=1 +3 41266078 COSM274695 G A . . GENE=CTNNB1;STRAND=+;CDS=c.75G>A;AA=p.W25*;CNT=1 +3 41266094 COSM730873 C A . . GENE=CTNNB1;STRAND=+;CDS=c.91C>A;AA=p.L31M;CNT=1 +3 41266097 COSM5668 G C . . GENE=CTNNB1;STRAND=+;CDS=c.94G>C;AA=p.D32H;CNT=2 +3 41266097 COSM5672 G A . . GENE=CTNNB1;STRAND=+;CDS=c.94G>A;AA=p.D32N;CNT=6 +3 41266097 COSM5661 G T . . GENE=CTNNB1;STRAND=+;CDS=c.94G>T;AA=p.D32Y;CNT=8 +3 41266098 COSM5690 A C . . GENE=CTNNB1;STRAND=+;CDS=c.95A>C;AA=p.D32A;CNT=4 +3 41266098 COSM5691 A T . . GENE=CTNNB1;STRAND=+;CDS=c.95A>T;AA=p.D32V;CNT=3 +3 41266098 COSM5681 A G . . GENE=CTNNB1;STRAND=+;CDS=c.95A>G;AA=p.D32G;CNT=9 +3 41266100 COSM5682 T C . . GENE=CTNNB1;STRAND=+;CDS=c.97T>C;AA=p.S33P;CNT=5 +3 41266100 COSM5683 T G . . GENE=CTNNB1;STRAND=+;CDS=c.97T>G;AA=p.S33A;CNT=1 +3 41266101 COSM5669 C T . . GENE=CTNNB1;STRAND=+;CDS=c.98C>T;AA=p.S33F;CNT=10 +3 41266101 COSM5677 C G . . GENE=CTNNB1;STRAND=+;CDS=c.98C>G;AA=p.S33C;CNT=13 +3 41266101 COSM5673 C A . . GENE=CTNNB1;STRAND=+;CDS=c.98C>A;AA=p.S33Y;CNT=5 +3 41266103 COSM5684 G C . . GENE=CTNNB1;STRAND=+;CDS=c.100G>C;AA=p.G34R;CNT=2 +3 41266103 COSM5686 G A . . GENE=CTNNB1;STRAND=+;CDS=c.100G>A;AA=p.G34R;CNT=13 +3 41266104 COSM5671 G A . . GENE=CTNNB1;STRAND=+;CDS=c.101G>A;AA=p.G34E;CNT=2 +3 41266104 COSM5670 G T . . GENE=CTNNB1;STRAND=+;CDS=c.101G>T;AA=p.G34V;CNT=7 +3 41266107 COSM5674 T G . . GENE=CTNNB1;STRAND=+;CDS=c.104T>G;AA=p.I35S;CNT=3 +3 41266109 COSM5703 C T . . GENE=CTNNB1;STRAND=+;CDS=c.106C>T;AA=p.H36Y;CNT=1 +3 41266110 COSM5678 A C . . GENE=CTNNB1;STRAND=+;CDS=c.107A>C;AA=p.H36P;CNT=1 +3 41266112 COSM5675 T G . . GENE=CTNNB1;STRAND=+;CDS=c.109T>G;AA=p.S37A;CNT=2 +3 41266112 COSM5687 T C . . GENE=CTNNB1;STRAND=+;CDS=c.109T>C;AA=p.S37P;CNT=3 +3 41266113 COSM5679 C G . . GENE=CTNNB1;STRAND=+;CDS=c.110C>G;AA=p.S37C;CNT=15 +3 41266113 COSM5662 C T . . GENE=CTNNB1;STRAND=+;CDS=c.110C>T;AA=p.S37F;CNT=13 +3 41266113 COSM5666 C A . . GENE=CTNNB1;STRAND=+;CDS=c.110C>A;AA=p.S37Y;CNT=3 +3 41266124 COSM5664 A G . . GENE=CTNNB1;STRAND=+;CDS=c.121A>G;AA=p.T41A;CNT=6 +3 41266125 COSM5730 C A . . GENE=CTNNB1;STRAND=+;CDS=c.122C>A;AA=p.T41N;CNT=4 +3 41266125 COSM5676 C T . . GENE=CTNNB1;STRAND=+;CDS=c.122C>T;AA=p.T41I;CNT=1 +3 41266128 COSM217270 C CCAGCTC . . GENE=CTNNB1;STRAND=+;CDS=c.125_126insCAGCTC;AA=p.T42_A43insSS;CNT=2 +3 41266134 COSM251368 C CAGCTCC . . GENE=CTNNB1;STRAND=+;CDS=c.131_132insAGCTCC;AA=p.P44_S45insAP;CNT=1 +3 41266136 COSM5685 T G . . GENE=CTNNB1;STRAND=+;CDS=c.133T>G;AA=p.S45A;CNT=2 +3 41266136 COSM5663 T C . . GENE=CTNNB1;STRAND=+;CDS=c.133T>C;AA=p.S45P;CNT=3 +3 41266137 COSM5667 C T . . GENE=CTNNB1;STRAND=+;CDS=c.134C>T;AA=p.S45F;CNT=7 +3 41266137 COSM5692 C A . . GENE=CTNNB1;STRAND=+;CDS=c.134C>A;AA=p.S45Y;CNT=4 +3 178916849 COSM582518 G T . . GENE=PIK3CA;STRAND=+;CDS=c.236G>T;AA=p.R79M;CNT=1 +3 178916849 COSM582517 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.236G>T;AA=p.R79M;CNT=1 +3 178916851 COSM163484 G A . . GENE=PIK3CA;STRAND=+;CDS=c.238G>A;AA=p.E80K;CNT=1 +3 178916854 COSM271871 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.241G>A;AA=p.E81K;CNT=3 +3 178916854 COSM27502 G A . . GENE=PIK3CA;STRAND=+;CDS=c.241G>A;AA=p.E81K;CNT=4 +3 178916861 COSM304777 T A . . GENE=PIK3CA;STRAND=+;CDS=c.248T>A;AA=p.F83Y;CNT=1 +3 178916861 COSM304778 T A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.248T>A;AA=p.F83Y;CNT=1 +3 178916876 COSM271684 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.263G>A;AA=p.R88Q;CNT=10 +3 178916876 COSM746 G A . . GENE=PIK3CA;STRAND=+;CDS=c.263G>A;AA=p.R88Q;CNT=13 +3 178916890 COSM1041455 C T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.277C>T;AA=p.R93W;CNT=2 +3 178916890 COSM27493 C T . . GENE=PIK3CA;STRAND=+;CDS=c.277C>T;AA=p.R93W;CNT=2 +3 178916891 COSM86041 G A . . GENE=PIK3CA;STRAND=+;CDS=c.278G>A;AA=p.R93Q;CNT=4 +3 178916891 COSM1041456 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.278G>A;AA=p.R93Q;CNT=4 +3 178916921 COSM214489 AACCAGTAGG A . . GENE=PIK3CA;STRAND=+;CDS=c.309_317delACCAGTAGG;AA=p.E103_G106>D;CNT=1 +3 178916924 COSM163485 C T . . GENE=PIK3CA;STRAND=+;CDS=c.311C>T;AA=p.P104L;CNT=1 +3 178916928 COSM445993 AGGCAACCGT A . . GENE=PIK3CA;STRAND=+;CDS=c.316_324delGGCAACCGT;AA=p.G106_R108delGNR;CNT=1 +3 178916928 COSM445992 AGGCAACCGT A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.316_324delGGCAACCGT;AA=p.G106_R108delGNR;CNT=1 +3 178916929 COSM86046 G C . . GENE=PIK3CA;STRAND=+;CDS=c.316G>C;AA=p.G106R;CNT=1 +3 178916929 COSM271872 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.316G>C;AA=p.G106R;CNT=1 +3 178916930 COSM748 G T . . GENE=PIK3CA;STRAND=+;CDS=c.317G>T;AA=p.G106V;CNT=1 +3 178916930 COSM729830 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.317G>T;AA=p.G106V;CNT=1 +3 178916933 COSM1041462 A G . . GENE=PIK3CA;STRAND=+;CDS=c.320A>G;AA=p.N107S;CNT=1 +3 178916933 COSM1041461 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.320A>G;AA=p.N107S;CNT=1 +3 178916936 COSM342716 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.323G>A;AA=p.R108H;CNT=4 +3 178916936 COSM729828 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.323G>T;AA=p.R108L;CNT=1 +3 178916936 COSM729829 G T . . GENE=PIK3CA;STRAND=+;CDS=c.323G>T;AA=p.R108L;CNT=1 +3 178916936 COSM27497 G A . . GENE=PIK3CA;STRAND=+;CDS=c.323G>A;AA=p.R108H;CNT=4 +3 178916943 COSM446000 AAAGATCCTC A . . GENE=PIK3CA;STRAND=+;CDS=c.331_339delAAGATCCTC;AA=p.K111_L113delKIL;CNT=1 +3 178916943 COSM445999 AAAGATCCTC A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.331_339delAAGATCCTC;AA=p.K111_L113delKIL;CNT=1 +3 178916944 COSM13570 A G . . GENE=PIK3CA;STRAND=+;CDS=c.331A>G;AA=p.K111E;CNT=5 +3 178916944 COSM1041463 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.331A>G;AA=p.K111E;CNT=5 +3 178916946 COSM12580 G C . . GENE=PIK3CA;STRAND=+;CDS=c.333G>C;AA=p.K111N;CNT=2 +3 178916946 COSM1041464 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.333G>T;AA=p.K111N;CNT=2 +3 178916946 COSM582516 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.333G>C;AA=p.K111N;CNT=1 +3 178916946 COSM27505 G T . . GENE=PIK3CA;STRAND=+;CDS=c.333G>T;AA=p.K111N;CNT=2 +3 178916949 COSM166154 CCTCAAT C . . GENE=PIK3CA;STRAND=+;CDS=c.337_342delCTCAAT;AA=p.L113_N114delLN;CNT=1 +3 178916957 COSM1041467 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.344G>T;AA=p.R115L;CNT=1 +3 178916957 COSM125368 G T . . GENE=PIK3CA;STRAND=+;CDS=c.344G>T;AA=p.R115L;CNT=2 +3 178921542 COSM582513 A T . . GENE=PIK3CA;STRAND=+;CDS=c.1024A>T;AA=p.T342S;CNT=1 +3 178921542 COSM582512 A T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1024A>T;AA=p.T342S;CNT=1 +3 178921548 COSM253280 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1030G>A;AA=p.V344M;CNT=3 +3 178921548 COSM253279 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1030G>A;AA=p.V344M;CNT=3 +3 178921549 COSM86951 T C . . GENE=PIK3CA;STRAND=+;CDS=c.1031T>C;AA=p.V344A;CNT=2 +3 178921549 COSM276750 T C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1031T>C;AA=p.V344A;CNT=2 +3 178921549 COSM258749 T G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1031T>G;AA=p.V344G;CNT=5 +3 178921549 COSM22540 T G . . GENE=PIK3CA;STRAND=+;CDS=c.1031T>G;AA=p.V344G;CNT=5 +3 178921552 COSM94979 A T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1034A>T;AA=p.N345I;CNT=1 +3 178921552 COSM94978 A T . . GENE=PIK3CA;STRAND=+;CDS=c.1034A>T;AA=p.N345I;CNT=1 +3 178921553 COSM132748 T A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1035T>A;AA=p.N345K;CNT=8 +3 178921553 COSM754 T A . . GENE=PIK3CA;STRAND=+;CDS=c.1035T>A;AA=p.N345K;CNT=10 +3 178921566 COSM582510 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1048G>A;AA=p.D350N;CNT=2 +3 178921566 COSM582511 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1048G>A;AA=p.D350N;CNT=2 +3 178921567 COSM271786 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1049A>G;AA=p.D350G;CNT=2 +3 178921567 COSM271785 A G . . GENE=PIK3CA;STRAND=+;CDS=c.1049A>G;AA=p.D350G;CNT=2 +3 178927974 COSM673907 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1252G>A;AA=p.E418K;CNT=1 +3 178927974 COSM12582 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1252G>A;AA=p.E418K;CNT=1 +3 178927977 COSM1220593 C A . . GENE=PIK3CA;STRAND=+;CDS=c.1255C>A;AA=p.H419N;CNT=1 +3 178927977 COSM1220592 C A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1255C>A;AA=p.H419N;CNT=1 +3 178927980 COSM757 T C . . GENE=PIK3CA;STRAND=+;CDS=c.1258T>C;AA=p.C420R;CNT=10 +3 178927980 COSM267862 T C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1258T>C;AA=p.C420R;CNT=7 +3 178928079 COSM12584 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1357G>A;AA=p.E453K;CNT=2 +3 178928079 COSM1041484 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1357G>C;AA=p.E453Q;CNT=2 +3 178928079 COSM446007 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1357G>A;AA=p.E453K;CNT=2 +3 178928079 COSM758 G C . . GENE=PIK3CA;STRAND=+;CDS=c.1357G>C;AA=p.E453Q;CNT=2 +3 178936070 COSM729821 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1612G>A;AA=p.D538N;CNT=1 +3 178936070 COSM21467 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1612G>A;AA=p.D538N;CNT=1 +3 178936074 COSM759 C G . . GENE=PIK3CA;STRAND=+;CDS=c.1616C>G;AA=p.P539R;CNT=1 +3 178936074 COSM446010 C G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1616C>G;AA=p.P539R;CNT=1 +3 178936082 COSM17442 G C . . GENE=PIK3CA;STRAND=+;CDS=c.1624G>C;AA=p.E542Q;CNT=2 +3 178936082 COSM326157 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1624G>C;AA=p.E542Q;CNT=2 +3 178936082 COSM760 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1624G>A;AA=p.E542K;CNT=29 +3 178936082 COSM125369 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1624G>A;AA=p.E542K;CNT=25 +3 178936083 COSM1041494 A C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1625A>C;AA=p.E542A;CNT=2 +3 178936083 COSM1041495 A C . . GENE=PIK3CA;STRAND=+;CDS=c.1625A>C;AA=p.E542A;CNT=2 +3 178936091 COSM295672 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1633G>C;AA=p.E545Q;CNT=1 +3 178936091 COSM763 G A . . GENE=PIK3CA;STRAND=+;CDS=c.1633G>A;AA=p.E545K;CNT=61 +3 178936091 COSM125370 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1633G>A;AA=p.E545K;CNT=51 +3 178936091 COSM27133 G C . . GENE=PIK3CA;STRAND=+;CDS=c.1633G>C;AA=p.E545Q;CNT=1 +3 178936092 COSM764 A G . . GENE=PIK3CA;STRAND=+;CDS=c.1634A>G;AA=p.E545G;CNT=5 +3 178936092 COSM297145 A C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1634A>C;AA=p.E545A;CNT=3 +3 178936092 COSM125371 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1634A>G;AA=p.E545G;CNT=5 +3 178936092 COSM12458 A C . . GENE=PIK3CA;STRAND=+;CDS=c.1634A>C;AA=p.E545A;CNT=4 +3 178936093 COSM765 G T . . GENE=PIK3CA;STRAND=+;CDS=c.1635G>T;AA=p.E545D;CNT=2 +3 178936093 COSM327064 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1635G>T;AA=p.E545D;CNT=2 +3 178936093 COSM27374 G C . . GENE=PIK3CA;STRAND=+;CDS=c.1635G>C;AA=p.E545D;CNT=1 +3 178936094 COSM255876 C A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1636C>A;AA=p.Q546K;CNT=7 +3 178936094 COSM766 C A . . GENE=PIK3CA;STRAND=+;CDS=c.1636C>A;AA=p.Q546K;CNT=9 +3 178936095 COSM12459 A G . . GENE=PIK3CA;STRAND=+;CDS=c.1637A>G;AA=p.Q546R;CNT=4 +3 178936095 COSM446012 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1637A>G;AA=p.Q546R;CNT=4 +3 178936095 COSM767 A C . . GENE=PIK3CA;STRAND=+;CDS=c.1637A>C;AA=p.Q546P;CNT=4 +3 178936095 COSM1041496 A C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1637A>C;AA=p.Q546P;CNT=3 +3 178936099 COSM729820 G C . . GENE=PIK3CA;STRAND=+;CDS=c.1641G>C;AA=p.E547D;CNT=1 +3 178936099 COSM729819 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.1641G>C;AA=p.E547D;CNT=1 +3 178938853 COSM397233 T A . . GENE=PIK3CA;STRAND=+;CDS=c.2095T>A;AA=p.L699M;CNT=1 +3 178938853 COSM397232 T A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.2095T>A;AA=p.L699M;CNT=1 +3 178938922 COSM1192506 G A . . GENE=PIK3CA;STRAND=+;CDS=c.2164G>A;AA=p.E722K;CNT=1 +3 178938931 COSM1041506 G A . . GENE=PIK3CA;STRAND=+;CDS=c.2173G>A;AA=p.D725N;CNT=1 +3 178938931 COSM1041505 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.2173G>A;AA=p.D725N;CNT=1 +3 178938934 COSM446019 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.2176G>A;AA=p.E726K;CNT=3 +3 178938934 COSM87306 G A . . GENE=PIK3CA;STRAND=+;CDS=c.2176G>A;AA=p.E726K;CNT=3 +3 178951903 COSM1220591 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.2958G>T;AA=p.K986N;CNT=1 +3 178951903 COSM87305 G T . . GENE=PIK3CA;STRAND=+;CDS=c.2958G>T;AA=p.K986N;CNT=1 +3 178951920 COSM1041514 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.2975G>C;AA=p.R992P;CNT=1 +3 178951920 COSM1041515 G C . . GENE=PIK3CA;STRAND=+;CDS=c.2975G>C;AA=p.R992P;CNT=1 +3 178951964 COSM94982 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3019G>C;AA=p.G1007R;CNT=1 +3 178951964 COSM17443 G C . . GENE=PIK3CA;STRAND=+;CDS=c.3019G>C;AA=p.G1007R;CNT=1 +3 178951994 COSM304026 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3049G>C;AA=p.D1017H;CNT=1 +3 178951994 COSM27377 G C . . GENE=PIK3CA;STRAND=+;CDS=c.3049G>C;AA=p.D1017H;CNT=1 +3 178952006 COSM17444 T C . . GENE=PIK3CA;STRAND=+;CDS=c.3061T>C;AA=p.Y1021H;CNT=1 +3 178952006 COSM246589 T C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3061T>C;AA=p.Y1021H;CNT=1 +3 178952007 COSM12461 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3062A>G;AA=p.Y1021C;CNT=2 +3 178952007 COSM276755 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3062A>G;AA=p.Y1021C;CNT=2 +3 178952018 COSM1041519 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3073A>G;AA=p.T1025A;CNT=2 +3 178952018 COSM771 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3073A>G;AA=p.T1025A;CNT=2 +3 178952024 COSM142978 GCC GTT . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3080_3081CC>TT;AA=p.A1027V;CNT=1 +3 178952024 COSM142977 GCC GTT . . GENE=PIK3CA;STRAND=+;CDS=c.3080_3081CC>TT;AA=p.A1027V;CNT=1 +3 178952064 COSM163486 T C . . GENE=PIK3CA;STRAND=+;CDS=c.3119T>C;AA=p.M1040T;CNT=1 +3 178952072 COSM94983 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3127A>G;AA=p.M1043V;CNT=3 +3 178952072 COSM12591 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3127A>G;AA=p.M1043V;CNT=4 +3 178952074 COSM419700 G T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3129G>T;AA=p.M1043I;CNT=1 +3 178952074 COSM29313 G A . . GENE=PIK3CA;STRAND=+;CDS=c.3129G>A;AA=p.M1043I;CNT=4 +3 178952074 COSM773 G T . . GENE=PIK3CA;STRAND=+;CDS=c.3129G>T;AA=p.M1043I;CNT=2 +3 178952074 COSM446027 G A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3129G>A;AA=p.M1043I;CNT=4 +3 178952077 COSM12592 T A . . GENE=PIK3CA;STRAND=+;CDS=c.3132T>A;AA=p.N1044K;CNT=2 +3 178952077 COSM479741 T A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3132T>A;AA=p.N1044K;CNT=2 +3 178952077 COSM1041522 T G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3132T>G;AA=p.N1044K;CNT=2 +3 178952077 COSM27504 T G . . GENE=PIK3CA;STRAND=+;CDS=c.3132T>G;AA=p.N1044K;CNT=2 +3 178952079 COSM729814 A T . . GENE=PIK3CA;STRAND=+;CDS=c.3134A>T;AA=p.D1045V;CNT=1 +3 178952079 COSM729813 A T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3134A>T;AA=p.D1045V;CNT=1 +3 178952084 COSM1041523 C T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3139C>T;AA=p.H1047Y;CNT=2 +3 178952084 COSM774 C T . . GENE=PIK3CA;STRAND=+;CDS=c.3139C>T;AA=p.H1047Y;CNT=2 +3 178952085 COSM775 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3140A>G;AA=p.H1047R;CNT=58 +3 178952085 COSM94986 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3140A>G;AA=p.H1047R;CNT=31 +3 178952085 COSM776 A T . . GENE=PIK3CA;STRAND=+;CDS=c.3140A>T;AA=p.H1047L;CNT=13 +3 178952085 COSM94987 A T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3140A>T;AA=p.H1047L;CNT=11 +3 178952088 COSM36289 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3143A>G;AA=p.H1048R;CNT=2 +3 178952088 COSM479742 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3143A>G;AA=p.H1048R;CNT=2 +3 178952090 COSM446029 G C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3145G>C;AA=p.G1049R;CNT=2 +3 178952090 COSM12597 G C . . GENE=PIK3CA;STRAND=+;CDS=c.3145G>C;AA=p.G1049R;CNT=3 +3 178952100 COSM1220594 C A . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3155C>A;AA=p.T1052K;CNT=1 +3 178952100 COSM17447 C A . . GENE=PIK3CA;STRAND=+;CDS=c.3155C>A;AA=p.T1052K;CNT=2 +3 178952117 COSM1177854 A T . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3172A>T;AA=p.I1058F;CNT=1 +3 178952117 COSM30606 A T . . GENE=PIK3CA;STRAND=+;CDS=c.3172A>T;AA=p.I1058F;CNT=1 +3 178952117 COSM479744 A C . . GENE=PIK3CA;STRAND=+;CDS=c.3172A>C;AA=p.I1058L;CNT=1 +3 178952117 COSM479743 A C . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3172A>C;AA=p.I1058L;CNT=1 +3 178952152 COSM17449 A G . . GENE=PIK3CA;STRAND=+;CDS=c.3207A>G;AA=p.*1069_*1069insWKDN*;CNT=1 +3 178952152 COSM1177856 A G . . GENE=PIK3CA_ENST00000263967;STRAND=+;CDS=c.3207A>G;AA=p.*1069W;CNT=1 +4 1803564 COSM1133721 C T . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.742C>T;AA=p.R248C;CNT=2 +4 1803564 COSM714 C T . . GENE=FGFR3;STRAND=+;CDS=c.742C>T;AA=p.R248C;CNT=2 +4 1803568 COSM1149892 C G . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.746C>G;AA=p.S249C;CNT=2 +4 1803568 COSM715 C G . . GENE=FGFR3;STRAND=+;CDS=c.746C>G;AA=p.S249C;CNT=2 +4 1803615 COSM107802 G A . . GENE=FGFR3;STRAND=+;CDS=c.793G>A;AA=p.A265T;CNT=1 +4 1803633 COSM1143544 G A . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.811G>A;AA=p.V271M;CNT=1 +4 1803633 COSM586608 G A . . GENE=FGFR3;STRAND=+;CDS=c.811G>A;AA=p.V271M;CNT=1 +4 1803640 COSM330456 T G . . GENE=FGFR3;STRAND=+;CDS=c.818T>G;AA=p.F273C;CNT=1 +4 1803661 COSM396078 A G . . GENE=FGFR3;STRAND=+;CDS=c.839A>G;AA=p.D280G;CNT=1 +4 1806119 COSM1133722 G A . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.1144G>A;AA=p.G382R;CNT=1 +4 1806119 COSM24842 G A . . GENE=FGFR3;STRAND=+;CDS=c.1138G>A;AA=p.G380R;CNT=1 +4 1806139 COSM123166 C G . . GENE=FGFR3;STRAND=+;CDS=c.1158C>G;AA=p.F386L;CNT=1 +4 1806176 COSM296687 C T . . GENE=FGFR3;STRAND=+;CDS=c.1195C>T;AA=p.R399C;CNT=1 +4 1806177 COSM340691 G A . . GENE=FGFR3;STRAND=+;CDS=c.1196G>A;AA=p.R399H;CNT=1 +4 1806227 COSM1143545 C A . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.1252C>A;AA=p.R418S;CNT=1 +4 1806227 COSM586607 C A . . GENE=FGFR3;STRAND=+;CDS=c.1246C>A;AA=p.R416S;CNT=1 +4 1807850 COSM481085 G T . . GENE=FGFR3;STRAND=+;CDS=c.1909G>T;AA=p.G637W;CNT=1 +4 1807850 COSM1137162 G T . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.1915G>T;AA=p.G639W;CNT=1 +4 1808386 COSM732992 A T . . GENE=FGFR3;STRAND=+;CDS=c.2144A>T;AA=p.K715M;CNT=1 +4 1808386 COSM1149893 A T . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.2150A>T;AA=p.K717M;CNT=1 +4 1808923 COSM1207091 C T . . GENE=FGFR3;STRAND=+;CDS=c.2355C>T;AA=p.D785D;CNT=1 +4 1808923 COSM1207090 C T . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.2361C>T;AA=p.D787D;CNT=1 +4 1808929 COSM1053512 C T . . GENE=FGFR3;STRAND=+;CDS=c.2361C>T;AA=p.S787S;CNT=1 +4 1808929 COSM1154329 C T . . GENE=FGFR3_ENST00000340107;STRAND=+;CDS=c.2367C>T;AA=p.S789S;CNT=1 +4 55141011 COSM335666 C G . . GENE=PDGFRA;STRAND=+;CDS=c.1657C>G;AA=p.P553A;CNT=1 +4 55141030 COSM345640 G T . . GENE=PDGFRA;STRAND=+;CDS=c.1676G>T;AA=p.W559L;CNT=1 +4 55141034 COSM298491 G A . . GENE=PDGFRA;STRAND=+;CDS=c.1680G>A;AA=p.R560R;CNT=1 +4 55141054 COSM191854 C T . . GENE=PDGFRA;STRAND=+;CDS=c.1700C>T;AA=p.P567L;CNT=1 +4 55141131 COSM734176 C A . . GENE=PDGFRA;STRAND=+;CDS=c.1777C>A;AA=p.L593I;CNT=1 +4 55144560 COSM257700 C A . . GENE=PDGFRA;STRAND=+;CDS=c.2034C>A;AA=p.F678L;CNT=1 +4 55144636 COSM191855 G T . . GENE=PDGFRA;STRAND=+;CDS=c.2110G>T;AA=p.E704*;CNT=1 +4 55144647 COSM80320 C A . . GENE=PDGFRA;STRAND=+;CDS=c.2121C>A;AA=p.I707I;CNT=1 +4 55152023 COSM217313 C A . . GENE=PDGFRA;STRAND=+;CDS=c.2455C>A;AA=p.L819M;CNT=2 +4 55152040 COSM22413 C T . . GENE=PDGFRA;STRAND=+;CDS=c.2472C>T;AA=p.V824V;CNT=1 +4 55152076 COSM734175 C G . . GENE=PDGFRA;STRAND=+;CDS=c.2508C>G;AA=p.D836E;CNT=1 +4 55152081 COSM378406 G T . . GENE=PDGFRA;STRAND=+;CDS=c.2513G>T;AA=p.G838V;CNT=1 +4 55152085 COSM587613 G T . . GENE=PDGFRA;STRAND=+;CDS=c.2517G>T;AA=p.L839L;CNT=1 +4 55152092 COSM734174 G C . . GENE=PDGFRA;STRAND=+;CDS=c.2524G>C;AA=p.D842H;CNT=1 +4 55561755 COSM1212554 C T . . GENE=KIT;STRAND=+;CDS=c.145C>T;AA=p.R49C;CNT=1 +4 55561756 COSM351040 G C . . GENE=KIT;STRAND=+;CDS=c.146G>C;AA=p.R49P;CNT=1 +4 55561758 COSM42898 G A . . GENE=KIT;STRAND=+;CDS=c.148G>A;AA=p.V50M;CNT=1 +4 55561763 COSM19025 C T . . GENE=KIT;STRAND=+;CDS=c.153C>T;AA=p.G51G;CNT=1 +4 55561765 COSM1212556 A G . . GENE=KIT;STRAND=+;CDS=c.155A>G;AA=p.D52G;CNT=1 +4 55561832 COSM167171 G A . . GENE=KIT;STRAND=+;CDS=c.222G>A;AA=p.T74T;CNT=1 +4 55561886 COSM295951 C T . . GENE=KIT;STRAND=+;CDS=c.276C>T;AA=p.T92T;CNT=1 +4 55592169 COSM192027 G A . . GENE=KIT;STRAND=+;CDS=c.1493G>A;AA=p.G498D;CNT=1 +4 55593452 COSM587606 T A . . GENE=KIT;STRAND=+;CDS=c.1609T>A;AA=p.C537S;CNT=2 +4 55593464 COSM28026 A C . . GENE=KIT;STRAND=+;CDS=c.1621A>C;AA=p.M541L;CNT=1 +4 55593588 COSM734168 A T . . GENE=KIT;STRAND=+;CDS=c.1654A>T;AA=p.M552L;CNT=1 +4 55593614 COSM734167 T A . . GENE=KIT;STRAND=+;CDS=c.1680T>A;AA=p.V560V;CNT=1 +4 55593639 COSM231534 GTTTACATAGACCCAACACAAC G . . GENE=KIT;STRAND=+;CDS=c.1706_1726del21;AA=p.Y570_L576delYIDPTQL;CNT=2 +4 55593644 COSM79375 C A . . GENE=KIT;STRAND=+;CDS=c.1710C>A;AA=p.Y570*;CNT=1 +4 55595518 COSM402445 A T . . GENE=KIT;STRAND=+;CDS=c.2008A>T;AA=p.T670S;CNT=1 +4 55595554 COSM240420 TT T . . GENE=KIT;STRAND=+;CDS=c.2045delT;AA=p.L682fs*1;CNT=1 +4 55595621 COSM1235167 A C . . GENE=KIT;STRAND=+;CDS=c.2111A>C;AA=p.K704T;CNT=1 +4 55597568 COSM1056106 G A . . GENE=KIT;STRAND=+;CDS=c.2216G>A;AA=p.R739K;CNT=1 +4 55599316 COSM171931 C T . . GENE=KIT;STRAND=+;CDS=c.2442C>T;AA=p.A814A;CNT=1 +4 55599352 COSM734165 A C . . GENE=KIT;STRAND=+;CDS=c.2478A>C;AA=p.K826N;CNT=1 +4 55599366 COSM734164 C G . . GENE=KIT;STRAND=+;CDS=c.2484+8C>G;AA=p.?;CNT=1 +4 55602676 COSM145558 G C . . GENE=KIT;STRAND=+;CDS=c.2497G>C;AA=p.V833L;CNT=1 +4 55602678 COSM175162 G T . . GENE=KIT;STRAND=+;CDS=c.2499G>T;AA=p.V833V;CNT=1 +4 55602719 COSM1212555 C T . . GENE=KIT;STRAND=+;CDS=c.2540C>T;AA=p.T847M;CNT=1 +4 55602747 COSM1056111 G T . . GENE=KIT;STRAND=+;CDS=c.2568G>T;AA=p.G856G;CNT=1 +4 55602765 COSM1325 G C . . GENE=KIT;STRAND=+;CDS=c.2586G>C;AA=p.L862L;CNT=1 +4 55602777 COSM1056112 T G . . GENE=KIT;STRAND=+;CDS=c.2596+2T>G;AA=p.?;CNT=1 +4 55946163 COSM587602 G T . . GENE=KDR;STRAND=-;CDS=c.4016C>A;AA=p.T1339K;CNT=1 +4 55946237 COSM128305 T A . . GENE=KDR;STRAND=-;CDS=c.3942A>T;AA=p.T1314T;CNT=1 +4 55953823 COSM734156 C A . . GENE=KDR;STRAND=-;CDS=c.3613G>T;AA=p.E1205*;CNT=1 +4 55953823 COSM384448 C T . . GENE=KDR;STRAND=-;CDS=c.3613G>A;AA=p.E1205K;CNT=1 +4 55953837 COSM447954 G T . . GENE=KDR;STRAND=-;CDS=c.3599C>A;AA=p.S1200Y;CNT=1 +4 55961023 COSM48464 C A . . GENE=KDR;STRAND=-;CDS=c.2917G>T;AA=p.A973S;CNT=2 +4 55961059 COSM213169 G A . . GENE=KDR;STRAND=-;CDS=c.2881C>T;AA=p.R961W;CNT=1 +4 55961077 COSM420569 T A . . GENE=KDR;STRAND=-;CDS=c.2863A>T;AA=p.I955F;CNT=1 +4 55961097 COSM138433 C T . . GENE=KDR;STRAND=-;CDS=c.2843G>A;AA=p.G948E;CNT=1 +4 55961098 COSM337898 C A . . GENE=KDR;STRAND=-;CDS=c.2842G>T;AA=p.G948W;CNT=1 +4 55961105 COSM420568 G A . . GENE=KDR;STRAND=-;CDS=c.2835C>T;AA=p.F945F;CNT=1 +4 55961110 COSM734153 G T . . GENE=KDR;STRAND=-;CDS=c.2830C>A;AA=p.R944R;CNT=1 +4 55962494 COSM734151 C A . . GENE=KDR;STRAND=-;CDS=c.2630G>T;AA=p.S877I;CNT=1 +4 55972974 COSM149673 T A . . GENE=KDR;STRAND=-;CDS=c.1416A>T;AA=p.Q472H;CNT=1 +4 55972980 COSM734142 A T . . GENE=KDR;STRAND=-;CDS=c.1413-3T>A;AA=p.?;CNT=1 +4 55979624 COSM734138 G A . . GENE=KDR;STRAND=-;CDS=c.823C>T;AA=p.R275*;CNT=1 +4 55979642 COSM447957 G A . . GENE=KDR;STRAND=-;CDS=c.805C>T;AA=p.H269Y;CNT=1 +4 55979649 COSM587581 C A . . GENE=KDR;STRAND=-;CDS=c.799-1G>T;AA=p.?;CNT=2 +4 153245430 COSM1137143 C T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1407G>A;AA=p.M469I;CNT=1 +4 153245430 COSM480955 C T . . GENE=FBXW7;STRAND=-;CDS=c.1761G>A;AA=p.M587I;CNT=1 +4 153245430 COSM480958 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.1044G>A;AA=p.M348I;CNT=1 +4 153245430 COSM480956 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1761G>A;AA=p.M587I;CNT=1 +4 153245430 COSM480957 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1521G>A;AA=p.M507I;CNT=1 +4 153245437 COSM732389 C G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1514G>C;AA=p.S505T;CNT=1 +4 153245437 COSM732388 C G . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1754G>C;AA=p.S585T;CNT=1 +4 153245437 COSM1149851 C G . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1400G>C;AA=p.S467T;CNT=1 +4 153245437 COSM732390 C G . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.1037G>C;AA=p.S346T;CNT=1 +4 153245437 COSM732387 C G . . GENE=FBXW7;STRAND=-;CDS=c.1754G>C;AA=p.S585T;CNT=1 +4 153245446 COSM295017 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.1028C>T;AA=p.S343L;CNT=4 +4 153245446 COSM1206897 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1391C>T;AA=p.S464L;CNT=2 +4 153245446 COSM295016 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1505C>T;AA=p.S502L;CNT=4 +4 153245446 COSM22979 G A . . GENE=FBXW7;STRAND=-;CDS=c.1745C>T;AA=p.S582L;CNT=4 +4 153245446 COSM295018 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1745C>T;AA=p.S582L;CNT=4 +4 153245450 COSM206691 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1741C>T;AA=p.Q581*;CNT=1 +4 153245450 COSM206689 G A . . GENE=FBXW7;STRAND=-;CDS=c.1741C>T;AA=p.Q581*;CNT=1 +4 153245450 COSM206688 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1501C>T;AA=p.Q501*;CNT=1 +4 153245450 COSM206690 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.1024C>T;AA=p.Q342*;CNT=1 +4 153245485 COSM336213 TCC TAA . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.987_988GG>TT;AA=p.V329>?;CNT=1 +4 153245485 COSM336212 TCC TAA . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1464_1465GG>TT;AA=p.V488>?;CNT=1 +4 153245485 COSM336211 TCC TAA . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1704_1705GG>TT;AA=p.V568>?;CNT=1 +4 153245485 COSM336210 TCC TAA . . GENE=FBXW7;STRAND=-;CDS=c.1704_1705GG>TT;AA=p.V568>?;CNT=1 +4 153245503 COSM84873 A G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1448T>C;AA=p.I483T;CNT=1 +4 153245503 COSM84874 A G . . GENE=FBXW7;STRAND=-;CDS=c.1688T>C;AA=p.I563T;CNT=1 +4 153245506 COSM222959 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1685C>T;AA=p.S562L;CNT=1 +4 153245506 COSM222957 G A . . GENE=FBXW7;STRAND=-;CDS=c.1685C>T;AA=p.S562L;CNT=1 +4 153245506 COSM222956 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1445C>T;AA=p.S482L;CNT=1 +4 153245506 COSM222958 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.968C>T;AA=p.S323L;CNT=1 +4 153245512 COSM1206898 T C . . GENE=FBXW7;STRAND=-;CDS=c.1679A>G;AA=p.D560G;CNT=1 +4 153245512 COSM1206901 T C . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1325A>G;AA=p.D442G;CNT=1 +4 153245512 COSM1206899 T C . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1679A>G;AA=p.D560G;CNT=1 +4 153245512 COSM1206902 T C . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.962A>G;AA=p.D321G;CNT=1 +4 153245512 COSM1206900 T C . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1439A>G;AA=p.D480G;CNT=1 +4 153247252 COSM732385 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1310G>A;AA=p.G437E;CNT=1 +4 153247252 COSM732384 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1550G>A;AA=p.G517E;CNT=1 +4 153247252 COSM732386 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.833G>A;AA=p.G278E;CNT=1 +4 153247252 COSM1149852 C T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1196G>A;AA=p.G399E;CNT=1 +4 153247252 COSM732383 C T . . GENE=FBXW7;STRAND=-;CDS=c.1550G>A;AA=p.G517E;CNT=1 +4 153247262 COSM305939 C A . . GENE=FBXW7;STRAND=-;CDS=c.1540G>T;AA=p.V514F;CNT=1 +4 153247262 COSM305941 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1540G>T;AA=p.V514F;CNT=1 +4 153247262 COSM305940 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.823G>T;AA=p.V275F;CNT=1 +4 153247262 COSM305938 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1300G>T;AA=p.V434F;CNT=1 +4 153247288 COSM133117 C T . . GENE=FBXW7;STRAND=-;CDS=c.1514G>A;AA=p.R505H;CNT=1 +4 153247288 COSM287372 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1274G>A;AA=p.R425H;CNT=1 +4 153247288 COSM287373 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.797G>A;AA=p.R266H;CNT=1 +4 153247288 COSM287374 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1514G>A;AA=p.R505H;CNT=1 +4 153247289 COSM22975 G A . . GENE=FBXW7;STRAND=-;CDS=c.1513C>T;AA=p.R505C;CNT=13 +4 153247289 COSM108571 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.796C>T;AA=p.R266C;CNT=12 +4 153247289 COSM732380 G T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1513C>A;AA=p.R505S;CNT=1 +4 153247289 COSM732381 G T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1273C>A;AA=p.R425S;CNT=1 +4 153247289 COSM1149853 G T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1159C>A;AA=p.R387S;CNT=1 +4 153247289 COSM74637 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1273C>T;AA=p.R425C;CNT=13 +4 153247289 COSM1133711 G C . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1159C>G;AA=p.R387G;CNT=6 +4 153247289 COSM99606 G C . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1513C>G;AA=p.R505G;CNT=8 +4 153247289 COSM108572 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1513C>T;AA=p.R505C;CNT=12 +4 153247289 COSM33763 G T . . GENE=FBXW7;STRAND=-;CDS=c.1513C>A;AA=p.R505S;CNT=1 +4 153247289 COSM1154290 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1159C>T;AA=p.R387C;CNT=7 +4 153247289 COSM99605 G C . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.796C>G;AA=p.R266G;CNT=8 +4 153247289 COSM99604 G C . . GENE=FBXW7;STRAND=-;CDS=c.1513C>G;AA=p.R505G;CNT=8 +4 153247289 COSM99603 G C . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1273C>G;AA=p.R425G;CNT=8 +4 153247289 COSM732382 G T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.796C>A;AA=p.R266S;CNT=1 +4 153247318 COSM172395 T G . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.767A>C;AA=p.H256P;CNT=1 +4 153247318 COSM172394 T G . . GENE=FBXW7;STRAND=-;CDS=c.1484A>C;AA=p.H495P;CNT=1 +4 153247318 COSM172396 T G . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1484A>C;AA=p.H495P;CNT=1 +4 153247318 COSM172393 T G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1244A>C;AA=p.H415P;CNT=1 +4 153247350 COSM123133 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1212G>T;AA=p.R404S;CNT=1 +4 153247350 COSM123134 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1452G>T;AA=p.R484S;CNT=1 +4 153247350 COSM123135 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.735G>T;AA=p.R245S;CNT=1 +4 153247350 COSM123132 C A . . GENE=FBXW7;STRAND=-;CDS=c.1452G>T;AA=p.R484S;CNT=1 +4 153247366 COSM420171 C G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1196G>C;AA=p.R399P;CNT=1 +4 153247366 COSM420169 C G . . GENE=FBXW7;STRAND=-;CDS=c.1436G>C;AA=p.R479P;CNT=1 +4 153247366 COSM1133712 C G . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1082G>C;AA=p.R361P;CNT=1 +4 153247366 COSM447498 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1436G>A;AA=p.R479Q;CNT=3 +4 153247366 COSM447499 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.719G>A;AA=p.R240Q;CNT=3 +4 153247366 COSM420172 C G . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.719G>C;AA=p.R240P;CNT=1 +4 153247366 COSM420170 C G . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1436G>C;AA=p.R479P;CNT=1 +4 153247366 COSM94297 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1196G>A;AA=p.R399Q;CNT=3 +4 153247366 COSM1154291 C T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1082G>A;AA=p.R361Q;CNT=3 +4 153247366 COSM22974 C T . . GENE=FBXW7;STRAND=-;CDS=c.1436G>A;AA=p.R479Q;CNT=3 +4 153247367 COSM206699 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1435C>T;AA=p.R479*;CNT=2 +4 153247367 COSM732376 G T . . GENE=FBXW7;STRAND=-;CDS=c.1435C>A;AA=p.R479R;CNT=1 +4 153247367 COSM732379 G T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.718C>A;AA=p.R240R;CNT=1 +4 153247367 COSM206697 G A . . GENE=FBXW7;STRAND=-;CDS=c.1435C>T;AA=p.R479*;CNT=2 +4 153247367 COSM732378 G T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1195C>A;AA=p.R399R;CNT=1 +4 153247367 COSM206696 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1195C>T;AA=p.R399*;CNT=2 +4 153247367 COSM1149855 G T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1081C>A;AA=p.R361R;CNT=1 +4 153247367 COSM1149854 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1081C>T;AA=p.R361*;CNT=1 +4 153247367 COSM732377 G T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1435C>A;AA=p.R479R;CNT=1 +4 153247367 COSM206698 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.718C>T;AA=p.R240*;CNT=2 +4 153247374 COSM206702 G T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.711C>A;AA=p.S237R;CNT=1 +4 153247374 COSM206701 G T . . GENE=FBXW7;STRAND=-;CDS=c.1428C>A;AA=p.S476R;CNT=1 +4 153247374 COSM206700 G T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1188C>A;AA=p.S396R;CNT=1 +4 153247374 COSM206703 G T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1428C>A;AA=p.S476R;CNT=1 +4 153247375 COSM1052087 C A . . GENE=FBXW7;STRAND=-;CDS=c.1427G>T;AA=p.S476I;CNT=1 +4 153247375 COSM1052088 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1427G>T;AA=p.S476I;CNT=1 +4 153247375 COSM1154292 C A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1073G>T;AA=p.S358I;CNT=1 +4 153247375 COSM1052089 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1187G>T;AA=p.S396I;CNT=1 +4 153247375 COSM1052090 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.710G>T;AA=p.S237I;CNT=1 +4 153249360 COSM24620 CT C . . GENE=FBXW7;STRAND=-;CDS=c.1417delA;AA=p.R473fs*25;CNT=1 +4 153249360 COSM292754 CT C . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1417delA;AA=p.R473fs*25;CNT=1 +4 153249360 COSM292753 CT C . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.700delA;AA=p.R234fs*25;CNT=1 +4 153249360 COSM292752 CT C . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1177delA;AA=p.R393fs*25;CNT=1 +4 153249366 COSM305935 T C . . GENE=FBXW7;STRAND=-;CDS=c.1412A>G;AA=p.E471G;CNT=1 +4 153249366 COSM305937 T C . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1412A>G;AA=p.E471G;CNT=1 +4 153249366 COSM305934 T C . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1172A>G;AA=p.E391G;CNT=1 +4 153249366 COSM305936 T C . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.695A>G;AA=p.E232G;CNT=1 +4 153249367 COSM305950 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1171G>T;AA=p.E391*;CNT=1 +4 153249367 COSM305951 C A . . GENE=FBXW7;STRAND=-;CDS=c.1411G>T;AA=p.E471*;CNT=1 +4 153249367 COSM305952 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.694G>T;AA=p.E232*;CNT=1 +4 153249367 COSM305953 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1411G>T;AA=p.E471*;CNT=1 +4 153249369 COSM1206890 T C . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1055A>G;AA=p.H352R;CNT=1 +4 153249369 COSM1206889 T C . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1169A>G;AA=p.H390R;CNT=1 +4 153249369 COSM1206887 T C . . GENE=FBXW7;STRAND=-;CDS=c.1409A>G;AA=p.H470R;CNT=1 +4 153249369 COSM1206891 T C . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.692A>G;AA=p.H231R;CNT=1 +4 153249369 COSM1206888 T C . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1409A>G;AA=p.H470R;CNT=1 +4 153249384 COSM673924 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.677G>T;AA=p.R226L;CNT=1 +4 153249384 COSM22965 C T . . GENE=FBXW7;STRAND=-;CDS=c.1394G>A;AA=p.R465H;CNT=16 +4 153249384 COSM673923 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1154G>T;AA=p.R385L;CNT=1 +4 153249384 COSM33762 C A . . GENE=FBXW7;STRAND=-;CDS=c.1394G>T;AA=p.R465L;CNT=1 +4 153249384 COSM117308 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1154G>A;AA=p.R385H;CNT=16 +4 153249384 COSM1149856 C T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1040G>A;AA=p.R347H;CNT=6 +4 153249384 COSM117309 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.677G>A;AA=p.R226H;CNT=16 +4 153249384 COSM117310 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1394G>A;AA=p.R465H;CNT=16 +4 153249384 COSM673925 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1394G>T;AA=p.R465L;CNT=1 +4 153249385 COSM22932 G A . . GENE=FBXW7;STRAND=-;CDS=c.1393C>T;AA=p.R465C;CNT=12 +4 153249385 COSM170725 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1153C>T;AA=p.R385C;CNT=12 +4 153249385 COSM1154293 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1039C>T;AA=p.R347C;CNT=6 +4 153249385 COSM170726 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.676C>T;AA=p.R226C;CNT=12 +4 153249385 COSM170727 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1393C>T;AA=p.R465C;CNT=12 +4 153249387 COSM403809 A T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1391T>A;AA=p.V464E;CNT=1 +4 153249387 COSM403808 A T . . GENE=FBXW7;STRAND=-;CDS=c.1391T>A;AA=p.V464E;CNT=1 +4 153249387 COSM403810 A T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1151T>A;AA=p.V384E;CNT=1 +4 153249387 COSM403811 A T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.674T>A;AA=p.V225E;CNT=1 +4 153249393 COSM1177867 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1031C>T;AA=p.S344F;CNT=1 +4 153249393 COSM1177864 G A . . GENE=FBXW7;STRAND=-;CDS=c.1385C>T;AA=p.S462F;CNT=1 +4 153249393 COSM1177868 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.668C>T;AA=p.S223F;CNT=1 +4 153249393 COSM1177866 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1145C>T;AA=p.S382F;CNT=1 +4 153249393 COSM1177865 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1385C>T;AA=p.S462F;CNT=1 +4 153249410 COSM1149857 G T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.1014C>A;AA=p.T338T;CNT=1 +4 153249410 COSM732372 G T . . GENE=FBXW7;STRAND=-;CDS=c.1368C>A;AA=p.T456T;CNT=1 +4 153249410 COSM732374 G T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1128C>A;AA=p.T376T;CNT=1 +4 153249410 COSM732373 G T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1368C>A;AA=p.T456T;CNT=1 +4 153249410 COSM732375 G T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.651C>A;AA=p.T217T;CNT=1 +4 153249440 COSM1158150 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1098G>T;AA=p.W366C;CNT=1 +4 153249440 COSM1158149 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1338G>T;AA=p.W446C;CNT=1 +4 153249440 COSM1158152 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.621G>T;AA=p.W207C;CNT=1 +4 153249440 COSM1158148 C A . . GENE=FBXW7;STRAND=-;CDS=c.1338G>T;AA=p.W446C;CNT=1 +4 153249440 COSM1158151 C A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.984G>T;AA=p.W328C;CNT=1 +4 153249456 COSM1177748 C G . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.605G>C;AA=p.R202P;CNT=1 +4 153249456 COSM1052091 C T . . GENE=FBXW7;STRAND=-;CDS=c.1322G>A;AA=p.R441Q;CNT=1 +4 153249456 COSM1177745 C G . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1322G>C;AA=p.R441P;CNT=1 +4 153249456 COSM1154294 C T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.968G>A;AA=p.R323Q;CNT=1 +4 153249456 COSM161024 C A . . GENE=FBXW7;STRAND=-;CDS=c.1322G>T;AA=p.R441L;CNT=1 +4 153249456 COSM161026 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1322G>T;AA=p.R441L;CNT=1 +4 153249456 COSM1052094 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.605G>A;AA=p.R202Q;CNT=1 +4 153249456 COSM1052092 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1322G>A;AA=p.R441Q;CNT=1 +4 153249456 COSM161023 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1082G>T;AA=p.R361L;CNT=1 +4 153249456 COSM1177744 C G . . GENE=FBXW7;STRAND=-;CDS=c.1322G>C;AA=p.R441P;CNT=1 +4 153249456 COSM161025 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.605G>T;AA=p.R202L;CNT=1 +4 153249456 COSM1052093 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1082G>A;AA=p.R361Q;CNT=1 +4 153249456 COSM1177746 C G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1082G>C;AA=p.R361P;CNT=1 +4 153249456 COSM1177747 C G . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.968G>C;AA=p.R323P;CNT=1 +4 153249469 COSM289996 C T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1069G>A;AA=p.G357R;CNT=1 +4 153249469 COSM289998 C T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.592G>A;AA=p.G198R;CNT=1 +4 153249469 COSM289997 C T . . GENE=FBXW7;STRAND=-;CDS=c.1309G>A;AA=p.G437R;CNT=1 +4 153249469 COSM289999 C T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1309G>A;AA=p.G437R;CNT=1 +4 153249501 COSM420168 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.560C>T;AA=p.S187L;CNT=1 +4 153249501 COSM420166 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1277C>T;AA=p.S426L;CNT=1 +4 153249501 COSM1133713 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.923C>T;AA=p.S308L;CNT=1 +4 153249501 COSM420165 G A . . GENE=FBXW7;STRAND=-;CDS=c.1277C>T;AA=p.S426L;CNT=1 +4 153249501 COSM420167 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1037C>T;AA=p.S346L;CNT=1 +4 153249510 COSM1052097 C A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.551G>T;AA=p.G184V;CNT=2 +4 153249510 COSM22984 C A . . GENE=FBXW7;STRAND=-;CDS=c.1268G>T;AA=p.G423V;CNT=2 +4 153249510 COSM1154295 C A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.914G>T;AA=p.G305V;CNT=2 +4 153249510 COSM1052095 C A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1268G>T;AA=p.G423V;CNT=2 +4 153249510 COSM1052096 C A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.1028G>T;AA=p.G343V;CNT=2 +4 153250855 COSM256125 GTGT G . . GENE=FBXW7;STRAND=-;CDS=c.1202_1204delACA;AA=p.N401delN;CNT=1 +4 153250855 COSM256127 GTGT G . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1202_1204delACA;AA=p.N401delN;CNT=1 +4 153250855 COSM256126 GTGT G . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.485_487delACA;AA=p.N162delN;CNT=1 +4 153250855 COSM256124 GTGT G . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.962_964delACA;AA=p.N321delN;CNT=1 +4 153250883 COSM1052103 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.937C>T;AA=p.R313*;CNT=1 +4 153250883 COSM22973 G A . . GENE=FBXW7;STRAND=-;CDS=c.1177C>T;AA=p.R393*;CNT=1 +4 153250883 COSM1052102 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.1177C>T;AA=p.R393*;CNT=1 +4 153250883 COSM1154296 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.823C>T;AA=p.R275*;CNT=1 +4 153250883 COSM1052104 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.460C>T;AA=p.R154*;CNT=1 +4 153258955 COSM271649 T A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.143A>T;AA=p.E48V;CNT=1 +4 153258955 COSM271650 T A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.860A>T;AA=p.E287V;CNT=1 +4 153258955 COSM271648 T A . . GENE=FBXW7;STRAND=-;CDS=c.860A>T;AA=p.E287V;CNT=1 +4 153258955 COSM271647 T A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.620A>T;AA=p.E207V;CNT=1 +4 153258983 COSM327087 G A . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.115C>T;AA=p.R39*;CNT=1 +4 153258983 COSM22971 G A . . GENE=FBXW7;STRAND=-;CDS=c.832C>T;AA=p.R278*;CNT=1 +4 153258983 COSM327086 G A . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.592C>T;AA=p.R198*;CNT=1 +4 153258983 COSM327088 G A . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.832C>T;AA=p.R278*;CNT=1 +4 153258983 COSM1173027 G A . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.478C>T;AA=p.R160*;CNT=1 +4 153259045 COSM1206883 A T . . GENE=FBXW7_ENST00000281708;STRAND=-;CDS=c.770T>A;AA=p.I257N;CNT=1 +4 153259045 COSM1206884 A T . . GENE=FBXW7_NM_018315_2;STRAND=-;CDS=c.530T>A;AA=p.I177N;CNT=1 +4 153259045 COSM1206885 A T . . GENE=FBXW7_ENST00000296555;STRAND=-;CDS=c.416T>A;AA=p.I139N;CNT=1 +4 153259045 COSM1206882 A T . . GENE=FBXW7;STRAND=-;CDS=c.770T>A;AA=p.I257N;CNT=1 +4 153259045 COSM1206886 A T . . GENE=FBXW7_ENST00000534231;STRAND=-;CDS=c.53T>A;AA=p.I18N;CNT=1 +5 112173893 COSM735077 G C . . GENE=APC;STRAND=+;CDS=c.2602G>C;AA=p.E868Q;CNT=1 +5 112173917 COSM18852 C T . . GENE=APC;STRAND=+;CDS=c.2626C>T;AA=p.R876*;CNT=18 +5 112173918 COSM1183183 G A . . GENE=APC;STRAND=+;CDS=c.2627G>A;AA=p.R876Q;CNT=2 +5 112173986 COSM256049 ACC A . . GENE=APC;STRAND=+;CDS=c.2696_2697delCC;AA=p.T899fs*12;CNT=1 +5 112173986 COSM1180984 AC A . . GENE=APC;STRAND=+;CDS=c.2696delC;AA=p.S900fs*16;CNT=2 +5 112173992 COSM201302 C T . . GENE=APC;STRAND=+;CDS=c.2701C>T;AA=p.Q901*;CNT=1 +5 112173995 COSM1178881 G T . . GENE=APC;STRAND=+;CDS=c.2704G>T;AA=p.E902*;CNT=1 +5 112174009 COSM1059578 T C . . GENE=APC;STRAND=+;CDS=c.2718T>C;AA=p.S906S;CNT=1 +5 112174022 COSM235665 G T . . GENE=APC;STRAND=+;CDS=c.2731G>T;AA=p.E911*;CNT=1 +5 112174043 COSM19065 G T . . GENE=APC;STRAND=+;CDS=c.2752G>T;AA=p.E918*;CNT=1 +5 112174061 COSM293047 A T . . GENE=APC;STRAND=+;CDS=c.2770A>T;AA=p.R924*;CNT=1 +5 112174062 COSM1194493 G A . . GENE=APC;STRAND=+;CDS=c.2771G>A;AA=p.R924K;CNT=1 +5 112174604 COSM235686 C T . . GENE=APC;STRAND=+;CDS=c.3313C>T;AA=p.R1105W;CNT=1 +5 112174611 COSM268675 C T . . GENE=APC;STRAND=+;CDS=c.3320C>T;AA=p.A1107V;CNT=1 +5 112174626 COSM108292 C A . . GENE=APC;STRAND=+;CDS=c.3335C>A;AA=p.T1112K;CNT=1 +5 112174631 COSM13125 C T . . GENE=APC;STRAND=+;CDS=c.3340C>T;AA=p.R1114*;CNT=8 +5 112174650 COSM387576 G C . . GENE=APC;STRAND=+;CDS=c.3359G>C;AA=p.G1120A;CNT=1 +5 112174650 COSM19329 G A . . GENE=APC;STRAND=+;CDS=c.3359G>A;AA=p.G1120E;CNT=1 +5 112174700 COSM462098 G C . . GENE=APC;STRAND=+;CDS=c.3409G>C;AA=p.D1137H;CNT=1 +5 112174742 COSM249227 G C . . GENE=APC;STRAND=+;CDS=c.3451G>C;AA=p.E1151Q;CNT=1 +5 112174745 COSM201304 C T . . GENE=APC;STRAND=+;CDS=c.3454C>T;AA=p.Q1152*;CNT=1 +5 112174762 COSM388400 G C . . GENE=APC;STRAND=+;CDS=c.3471G>C;AA=p.E1157D;CNT=1 +5 112174774 COSM256325 T G . . GENE=APC;STRAND=+;CDS=c.3483T>G;AA=p.N1161K;CNT=1 +5 112175052 COSM201306 T A . . GENE=APC;STRAND=+;CDS=c.3761T>A;AA=p.I1254N;CNT=1 +5 112175060 COSM169041 G T . . GENE=APC;STRAND=+;CDS=c.3769G>T;AA=p.E1257*;CNT=1 +5 112175069 COSM256144 C T . . GENE=APC;STRAND=+;CDS=c.3778C>T;AA=p.Q1260*;CNT=1 +5 112175101 COSM290422 T A . . GENE=APC;STRAND=+;CDS=c.3810T>A;AA=p.C1270*;CNT=1 +5 112175133 COSM19212 C A . . GENE=APC;STRAND=+;CDS=c.3842C>A;AA=p.S1281*;CNT=1 +5 112175136 COSM23576 C G . . GENE=APC;STRAND=+;CDS=c.3845C>G;AA=p.S1282*;CNT=1 +5 112175147 COSM18772 G T . . GENE=APC;STRAND=+;CDS=c.3856G>T;AA=p.E1286*;CNT=1 +5 112175148 COSM116903 A G . . GENE=APC;STRAND=+;CDS=c.3857A>G;AA=p.E1286G;CNT=1 +5 112175153 COSM19577 G T . . GENE=APC;STRAND=+;CDS=c.3862G>T;AA=p.G1288*;CNT=1 +5 112175161 COSM1183188 T A . . GENE=APC;STRAND=+;CDS=c.3870T>A;AA=p.N1290K;CNT=2 +5 112175161 COSM1180985 TC T . . GENE=APC;STRAND=+;CDS=c.3871delC;AA=p.Q1291fs*14;CNT=2 +5 112175167 COSM19579 GAC G . . GENE=APC;STRAND=+;CDS=c.3877_3878delAC;AA=p.Q1294fs*6;CNT=1 +5 112175171 COSM18960 C T . . GENE=APC;STRAND=+;CDS=c.3880C>T;AA=p.Q1294*;CNT=3 +5 112175174 COSM18961 G T . . GENE=APC;STRAND=+;CDS=c.3883G>T;AA=p.E1295*;CNT=1 +5 112175174 COSM293282 GA G . . GENE=APC;STRAND=+;CDS=c.3884delA;AA=p.A1296fs*9;CNT=1 +5 112175192 COSM300845 AC A . . GENE=APC;STRAND=+;CDS=c.3902delC;AA=p.L1302fs*3;CNT=1 +5 112175198 COSM13728 C T . . GENE=APC;STRAND=+;CDS=c.3907C>T;AA=p.Q1303*;CNT=1 +5 112175202 COSM23582 TA T . . GENE=APC;STRAND=+;CDS=c.3912delA;AA=p.I1304fs*4;CNT=1 +5 112175207 COSM18760 G T . . GENE=APC;STRAND=+;CDS=c.3916G>T;AA=p.E1306*;CNT=5 +5 112175211 COSM18764 TAAAAG T . . GENE=APC;STRAND=+;CDS=c.3921_3925delAAAAG;AA=p.E1309fs*4;CNT=3 +5 112175216 COSM18775 G T . . GENE=APC;STRAND=+;CDS=c.3925G>T;AA=p.E1309*;CNT=2 +5 112175216 COSM288539 GAA G . . GENE=APC;STRAND=+;CDS=c.3926_3927delAA;AA=p.K1310fs*4;CNT=1 +5 112175222 COSM292899 ATT A . . GENE=APC;STRAND=+;CDS=c.3932_3933delTT;AA=p.I1311fs*3;CNT=1 +5 112175225 COSM18817 G T . . GENE=APC;STRAND=+;CDS=c.3934G>T;AA=p.G1312*;CNT=2 +5 112175225 COSM588988 G C . . GENE=APC;STRAND=+;CDS=c.3934G>C;AA=p.G1312R;CNT=1 +5 112175226 COSM300648 G GA . . GENE=APC;STRAND=+;CDS=c.3935_3936insA;AA=p.T1313fs*2;CNT=1 +5 112175235 COSM18777 C A . . GENE=APC;STRAND=+;CDS=c.3944C>A;AA=p.S1315*;CNT=2 +5 112175245 COSM287761 TC T . . GENE=APC;STRAND=+;CDS=c.3955delC;AA=p.P1319fs*2;CNT=1 +5 112175246 COSM392372 CCTGTGAGCGA C . . GENE=APC;STRAND=+;CDS=c.3956_3965del10;AA=p.P1319fs*93;CNT=1 +5 112175247 COSM19010 C T . . GENE=APC;STRAND=+;CDS=c.3956C>T;AA=p.P1319L;CNT=1 +5 112175255 COSM18702 G T . . GENE=APC;STRAND=+;CDS=c.3964G>T;AA=p.E1322*;CNT=2 +5 112175273 COSM18859 C T . . GENE=APC;STRAND=+;CDS=c.3982C>T;AA=p.Q1328*;CNT=2 +5 112175301 COSM304960 TGC TCT . . GENE=APC;STRAND=+;CDS=c.4011_4012GC>CT;AA=p.Q1338*;CNT=1 +5 112175303 COSM13129 C T . . GENE=APC;STRAND=+;CDS=c.4012C>T;AA=p.Q1338*;CNT=6 +5 112175328 COSM25826 C G . . GENE=APC;STRAND=+;CDS=c.4037C>G;AA=p.S1346*;CNT=2 +5 112175328 COSM19084 C A . . GENE=APC;STRAND=+;CDS=c.4037C>A;AA=p.S1346*;CNT=1 +5 112175330 COSM223025 G A . . GENE=APC;STRAND=+;CDS=c.4039G>A;AA=p.A1347T;CNT=1 +5 112175345 COSM295899 GT G . . GENE=APC;STRAND=+;CDS=c.4055delT;AA=p.E1353fs*62;CNT=1 +5 112175348 COSM19048 G T . . GENE=APC;STRAND=+;CDS=c.4057G>T;AA=p.E1353*;CNT=2 +5 112175350 COSM292626 AT A . . GENE=APC;STRAND=+;CDS=c.4060delT;AA=p.S1355fs*60;CNT=2 +5 112175355 COSM1183191 C A . . GENE=APC;STRAND=+;CDS=c.4064C>A;AA=p.S1355Y;CNT=2 +5 112175358 COSM18779 C G . . GENE=APC;STRAND=+;CDS=c.4067C>G;AA=p.S1356*;CNT=1 +5 112175378 COSM18797 A T . . GENE=APC;STRAND=+;CDS=c.4087A>T;AA=p.K1363*;CNT=1 +5 112175390 COSM13121 C T . . GENE=APC;STRAND=+;CDS=c.4099C>T;AA=p.Q1367*;CNT=6 +5 112175398 COSM295587 C A . . GENE=APC;STRAND=+;CDS=c.4107C>A;AA=p.P1369P;CNT=1 +5 112175399 COSM18758 A T . . GENE=APC;STRAND=+;CDS=c.4108A>T;AA=p.K1370*;CNT=1 +5 112175411 COSM19085 G T . . GENE=APC;STRAND=+;CDS=c.4120G>T;AA=p.E1374*;CNT=3 +5 112175419 COSM18861 T A . . GENE=APC;STRAND=+;CDS=c.4128T>A;AA=p.Y1376*;CNT=1 +5 112175423 COSM18862 C T . . GENE=APC;STRAND=+;CDS=c.4132C>T;AA=p.Q1378*;CNT=10 +5 112175423 COSM290350 CA C . . GENE=APC;STRAND=+;CDS=c.4133delA;AA=p.Q1378fs*37;CNT=1 +5 112175426 COSM18834 G T . . GENE=APC;STRAND=+;CDS=c.4135G>T;AA=p.E1379*;CNT=3 +5 112175429 COSM19584 A AC . . GENE=APC;STRAND=+;CDS=c.4138_4139insC;AA=p.L1382fs*4;CNT=1 +5 112175432 COSM143913 C T . . GENE=APC;STRAND=+;CDS=c.4141C>T;AA=p.P1381S;CNT=1 +5 112175438 COSM256050 A AT . . GENE=APC;STRAND=+;CDS=c.4147_4148insT;AA=p.M1383fs*3;CNT=1 +5 112175446 COSM19586 C CAGAT . . GENE=APC;STRAND=+;CDS=c.4155_4156insAGAT;AA=p.C1387fs*1;CNT=1 +5 112175447 COSM18864 A T . . GENE=APC;STRAND=+;CDS=c.4156A>T;AA=p.R1386*;CNT=2 +5 112175468 COSM735074 C A . . GENE=APC;STRAND=+;CDS=c.4177C>A;AA=p.L1393I;CNT=1 +5 112175480 COSM18865 G T . . GENE=APC;STRAND=+;CDS=c.4189G>T;AA=p.E1397*;CNT=1 +5 112175483 COSM295697 AG A . . GENE=APC;STRAND=+;CDS=c.4193delG;AA=p.S1398fs*17;CNT=1 +5 112175487 COSM201307 G A . . GENE=APC;STRAND=+;CDS=c.4196G>A;AA=p.R1399H;CNT=1 +5 112175489 COSM19051 TC T . . GENE=APC;STRAND=+;CDS=c.4199delC;AA=p.S1400fs*1;CNT=1 +5 112175490 COSM171089 C T . . GENE=APC;STRAND=+;CDS=c.4199C>T;AA=p.S1400L;CNT=3 +5 112175494 COSM242996 T C . . GENE=APC;STRAND=+;CDS=c.4203T>C;AA=p.I1401I;CNT=1 +5 112175497 COSM1137229 C T . . GENE=APC;STRAND=+;CDS=c.4206C>T;AA=p.A1402A;CNT=1 +5 112175507 COSM19087 C T . . GENE=APC;STRAND=+;CDS=c.4216C>T;AA=p.Q1406*;CNT=3 +5 112175513 COSM18822 G T . . GENE=APC;STRAND=+;CDS=c.4222G>T;AA=p.E1408*;CNT=5 +5 112175520 COSM292171 G C . . GENE=APC;STRAND=+;CDS=c.4229G>C;AA=p.C1410S;CNT=1 +5 112175521 COSM19592 C A . . GENE=APC;STRAND=+;CDS=c.4230C>A;AA=p.C1410*;CNT=1 +5 112175523 COSM18948 GT G . . GENE=APC;STRAND=+;CDS=c.4233delT;AA=p.S1411fs*4;CNT=1 +5 112175529 COSM18887 TG T . . GENE=APC;STRAND=+;CDS=c.4239delG;AA=p.V1414fs*1;CNT=2 +5 112175531 COSM27577 G A . . GENE=APC;STRAND=+;CDS=c.4240G>A;AA=p.V1414I;CNT=1 +5 112175547 COSM300272 G A . . GENE=APC;STRAND=+;CDS=c.4256G>A;AA=p.S1419N;CNT=1 +5 112175547 COSM1180986 GCC G . . GENE=APC;STRAND=+;CDS=c.4257_4258delCC;AA=p.P1420fs*2;CNT=2 +5 112175551 COSM19278 CA C . . GENE=APC;STRAND=+;CDS=c.4261delA;AA=p.S1421fs*52;CNT=1 +5 112175552 COSM295636 AG A . . GENE=APC;STRAND=+;CDS=c.4262delG;AA=p.S1421fs*52;CNT=1 +5 112175576 COSM18836 C T . . GENE=APC;STRAND=+;CDS=c.4285C>T;AA=p.Q1429*;CNT=1 +5 112175577 COSM69686 A G . . GENE=APC;STRAND=+;CDS=c.4286A>G;AA=p.Q1429R;CNT=1 +5 112175593 COSM301342 CA C . . GENE=APC;STRAND=+;CDS=c.4303delA;AA=p.R1435fs*38;CNT=1 +5 112175604 COSM19053 CAC C . . GENE=APC;STRAND=+;CDS=c.4314_4315delAC;AA=p.P1439fs*15;CNT=1 +5 112175604 COSM296347 CA C . . GENE=APC;STRAND=+;CDS=c.4314delA;AA=p.P1439fs*34;CNT=1 +5 112175639 COSM13127 C T . . GENE=APC;STRAND=+;CDS=c.4348C>T;AA=p.R1450*;CNT=27 +5 112175649 COSM287333 C CTT . . GENE=APC;STRAND=+;CDS=c.4358_4359insTT;AA=p.K1454fs*20;CNT=1 +5 112175651 COSM27993 A G . . GENE=APC;STRAND=+;CDS=c.4360A>G;AA=p.K1454E;CNT=1 +5 112175675 COSM18873 AAG A . . GENE=APC;STRAND=+;CDS=c.4385_4386delAG;AA=p.S1465fs*3;CNT=1 +5 112175678 COSM159119 A T . . GENE=APC;STRAND=+;CDS=c.4387A>T;AA=p.R1463*;CNT=1 +5 112175696 COSM18729 C T . . GENE=APC;STRAND=+;CDS=c.4405C>T;AA=p.Q1469*;CNT=1 +5 112175745 COSM19708 CT C . . GENE=APC;STRAND=+;CDS=c.4455delT;AA=p.D1486fs*21;CNT=2 +5 112175751 COSM19288 CTTTA C . . GENE=APC;STRAND=+;CDS=c.4461_4464delTTTA;AA=p.L1488fs*18;CNT=2 +5 112175751 COSM18999 CT C . . GENE=APC;STRAND=+;CDS=c.4461delT;AA=p.L1488fs*19;CNT=3 +5 112175757 COSM291723 T A . . GENE=APC;STRAND=+;CDS=c.4466T>A;AA=p.L1489*;CNT=1 +5 112175760 COSM19623 AT A . . GENE=APC;STRAND=+;CDS=c.4470delT;AA=p.F1491fs*16;CNT=1 +5 112175830 COSM1173082 GC G . . GENE=APC;STRAND=+;CDS=c.4540delC;AA=p.P1514fs*9;CNT=3 +5 112175852 COSM1183180 G T . . GENE=APC;STRAND=+;CDS=c.4561G>T;AA=p.E1521*;CNT=2 +5 112175876 COSM1183187 C T . . GENE=APC;STRAND=+;CDS=c.4585C>T;AA=p.Q1529*;CNT=2 +5 112175897 COSM19056 G T . . GENE=APC;STRAND=+;CDS=c.4606G>T;AA=p.E1536*;CNT=1 +5 112175910 COSM238808 AG A . . GENE=APC;STRAND=+;CDS=c.4620delG;AA=p.E1540fs*25;CNT=1 +5 112175921 COSM462097 G C . . GENE=APC;STRAND=+;CDS=c.4630G>C;AA=p.E1544Q;CNT=1 +5 112175947 COSM238809 G GAAGAG . . GENE=APC;STRAND=+;CDS=c.4656_4657insAAGAG;AA=p.A1553fs*14;CNT=1 +5 112175951 COSM19695 G GA . . GENE=APC;STRAND=+;CDS=c.4660_4661insA;AA=p.T1556fs*3;CNT=2 +5 112175957 COSM18561 A AA . . GENE=APC;STRAND=+;CDS=c.4666_4667insA;AA=p.T1556fs*3;CNT=2 +5 112175969 COSM273730 G GA . . GENE=APC;STRAND=+;CDS=c.4678_4679insA;AA=p.D1562fs*5;CNT=1 +5 112175975 COSM588987 G A . . GENE=APC;STRAND=+;CDS=c.4684G>A;AA=p.D1562N;CNT=1 +5 112175978 COSM242471 CT C . . GENE=APC;STRAND=+;CDS=c.4688delT;AA=p.L1563fs*2;CNT=1 +5 112176002 COSM1194540 G T . . GENE=APC;STRAND=+;CDS=c.4711G>T;AA=p.D1571Y;CNT=1 +5 112176007 COSM251382 T TT . . GENE=APC;STRAND=+;CDS=c.4716_4717insT;AA=p.E1573fs*1;CNT=1 +5 112176008 COSM267970 GA G . . GENE=APC;STRAND=+;CDS=c.4718delA;AA=p.I1574fs*2;CNT=1 +5 112176017 COSM236691 G T . . GENE=APC;STRAND=+;CDS=c.4726G>T;AA=p.E1576*;CNT=1 +5 149433673 COSM310349 C T . . GENE=CSF1R;STRAND=-;CDS=c.2878G>A;AA=p.A960T;CNT=1 +5 149433673 COSM310350 C T . . GENE=CSF1R_ENST00000286301;STRAND=-;CDS=c.2878G>A;AA=p.A960T;CNT=1 +5 170837543 COSM158604 C CTCTG . . GENE=NPM1;STRAND=+;CDS=c.859_860insTCTG;AA=p.W288fs*>9;CNT=4 +5 170837543 COSM46518 C CTCGC . . GENE=NPM1;STRAND=+;CDS=c.859_860insTCGC;AA=p.W288fs*12;CNT=1 +5 170837545 COSM158600 C CTGCA . . GENE=NPM1;STRAND=+;CDS=c.861_862insTGCA;AA=p.W288fs*>9;CNT=2 +5 170837547 COSM17573 G GCCTG . . GENE=NPM1;STRAND=+;CDS=c.863_864insCCTG;AA=p.W288fs*12;CNT=2 +5 170837547 COSM17559 G GTCTG . . GENE=NPM1;STRAND=+;CDS=c.863_864insTCTG;AA=p.W288fs*12;CNT=15 +5 170837547 COSM20856 G GTCAG . . GENE=NPM1;STRAND=+;CDS=c.863_864insTCAG;AA=p.W288fs*12;CNT=1 +5 170837547 COSM17571 G GCATG . . GENE=NPM1;STRAND=+;CDS=c.863_864insCATG;AA=p.W288fs*12;CNT=3 +7 55211097 COSM174732 G A . . GENE=EGFR;STRAND=+;CDS=c.340G>A;AA=p.E114K;CNT=1 +7 55211097 COSM174733 G A . . GENE=EGFR_ENST00000344576;STRAND=+;CDS=c.340G>A;AA=p.E114K;CNT=1 +7 55221800 COSM453244 G A . . GENE=EGFR_ENST00000344576;STRAND=+;CDS=c.844G>A;AA=p.E282K;CNT=1 +7 55221800 COSM453243 G A . . GENE=EGFR;STRAND=+;CDS=c.844G>A;AA=p.E282K;CNT=1 +7 55233037 COSM21689 C T . . GENE=EGFR;STRAND=+;CDS=c.1787C>T;AA=p.P596L;CNT=1 +7 55233037 COSM191988 C T . . GENE=EGFR_ENST00000344576;STRAND=+;CDS=c.1787C>T;AA=p.P596L;CNT=1 +7 55233043 COSM21690 G T . . GENE=EGFR;STRAND=+;CDS=c.1793G>T;AA=p.G598V;CNT=1 +7 55233043 COSM1187304 G T . . GENE=EGFR_ENST00000344576;STRAND=+;CDS=c.1793G>T;AA=p.G598V;CNT=1 +7 55241677 COSM116882 G C . . GENE=EGFR;STRAND=+;CDS=c.2125G>C;AA=p.E709Q;CNT=1 +7 55241678 COSM51525 AAAC A . . GENE=EGFR;STRAND=+;CDS=c.2127_2129delAAC;AA=p.E709_T710>D;CNT=1 +7 55241699 COSM116797 A G . . GENE=EGFR;STRAND=+;CDS=c.2147A>G;AA=p.K716R;CNT=1 +7 55241708 COSM6239 G C . . GENE=EGFR;STRAND=+;CDS=c.2156G>C;AA=p.G719A;CNT=5 +7 55241711 COSM747426 C G . . GENE=EGFR;STRAND=+;CDS=c.2159C>G;AA=p.S720C;CNT=1 +7 55242454 COSM1090888 G A . . GENE=EGFR;STRAND=+;CDS=c.2224G>A;AA=p.V742I;CNT=1 +7 55242463 COSM1190791 AAGGAATTAAGAGAAG A . . GENE=EGFR;STRAND=+;CDS=c.2234_2248del15;AA=p.K745_A750>T;CNT=4 +7 55242464 COSM6223 AGGAATTAAGAGAAGC A . . GENE=EGFR;STRAND=+;CDS=c.2235_2249del15;AA=p.E746_A750delELREA;CNT=7 +7 55242465 COSM6225 GGAATTAAGAGAAGCA G . . GENE=EGFR;STRAND=+;CDS=c.2236_2250del15;AA=p.E746_A750delELREA;CNT=2 +7 55242465 COSM12728 GGAATTAAGAGAAGCAACA G . . GENE=EGFR;STRAND=+;CDS=c.2236_2253del18;AA=p.E746_T751delELREAT;CNT=2 +7 55242467 COSM6220 AATTAAGAGAAGCAACATC A . . GENE=EGFR;STRAND=+;CDS=c.2238_2255del18;AA=p.E746_S752>D;CNT=1 +7 55242467 COSM392194 AATTAAGAGAAGCAAC A . . GENE=EGFR;STRAND=+;CDS=c.2238_2252del15;AA=p.L747_T751delLREAT;CNT=1 +7 55242468 COSM6255 ATTAAGAGAAGCAACATCT A . . GENE=EGFR;STRAND=+;CDS=c.2239_2256del18;AA=p.L747_S752delLREATS;CNT=1 +7 55242470 COSM26704 T C . . GENE=EGFR;STRAND=+;CDS=c.2240T>C;AA=p.L747S;CNT=1 +7 55242489 COSM601575 G T . . GENE=EGFR;STRAND=+;CDS=c.2259G>T;AA=p.P753P;CNT=1 +7 55248998 COSM392166 A AN . . GENE=EGFR;STRAND=+;CDS=c.2296_2297insTGGCCAGCG;AA=p.V769_D770insASV;CNT=1 +7 55249005 COSM6241 G T . . GENE=EGFR;STRAND=+;CDS=c.2303G>T;AA=p.S768I;CNT=3 +7 55249005 COSM291998 G C . . GENE=EGFR;STRAND=+;CDS=c.2303G>C;AA=p.S768T;CNT=1 +7 55249007 COSM6242 G T . . GENE=EGFR;STRAND=+;CDS=c.2305G>T;AA=p.V769L;CNT=1 +7 55249017 COSM115794 C G . . GENE=EGFR;STRAND=+;CDS=c.2315C>G;AA=p.P772R;CNT=1 +7 55249017 COSM404810 C CN . . GENE=EGFR;STRAND=+;CDS=c.2315_2316insCCACGT;AA=p.V774_C775insHV;CNT=1 +7 55249029 COSM22940 G A . . GENE=EGFR;STRAND=+;CDS=c.2327G>A;AA=p.R776H;CNT=1 +7 55249071 COSM6240 C T . . GENE=EGFR;STRAND=+;CDS=c.2369C>T;AA=p.T790M;CNT=2 +7 55249083 COSM244213 C A . . GENE=EGFR;STRAND=+;CDS=c.2381C>A;AA=p.P794H;CNT=1 +7 55249108 COSM747425 CCG CAT . . GENE=EGFR;STRAND=+;CDS=c.2407_2408CG>AT;AA=p.R803M;CNT=1 +7 55249116 COSM485464 A G . . GENE=EGFR;STRAND=+;CDS=c.2414A>G;AA=p.H805R;CNT=1 +7 55249134 COSM1187305 C T . . GENE=EGFR;STRAND=+;CDS=c.2432C>T;AA=p.S811F;CNT=1 +7 55259501 COSM53231 C T . . GENE=EGFR;STRAND=+;CDS=c.2559C>T;AA=p.I853I;CNT=1 +7 55259512 COSM370916 G T . . GENE=EGFR;STRAND=+;CDS=c.2570G>T;AA=p.G857V;CNT=1 +7 55259515 COSM6224 T G . . GENE=EGFR;STRAND=+;CDS=c.2573T>G;AA=p.L858R;CNT=30 +7 55259524 COSM6213 T A . . GENE=EGFR;STRAND=+;CDS=c.2582T>A;AA=p.L861Q;CNT=5 +7 116339711 COSM201897 G A . . GENE=MET;STRAND=+;CDS=c.573G>A;AA=p.R191R;CNT=1 +7 116339714 COSM1214926 C A . . GENE=MET;STRAND=+;CDS=c.576C>A;AA=p.F192L;CNT=1 +7 116339746 COSM282765 C A . . GENE=MET;STRAND=+;CDS=c.608C>A;AA=p.S203Y;CNT=1 +7 116339776 COSM257403 C T . . GENE=MET;STRAND=+;CDS=c.638C>T;AA=p.S213L;CNT=1 +7 116340287 COSM744049 G T . . GENE=MET;STRAND=+;CDS=c.1149G>T;AA=p.V383V;CNT=1 +7 116412023 COSM339515 A T . . GENE=MET;STRAND=+;CDS=c.3062A>T;AA=p.Y1021F;CNT=1 +7 116412024 COSM598583 C G . . GENE=MET;STRAND=+;CDS=c.3063C>G;AA=p.Y1021*;CNT=1 +7 116412044 COSM88794 G T . . GENE=MET;STRAND=+;CDS=c.3082+1G>T;AA=p.?;CNT=1 +7 116412045 COSM35468 T C . . GENE=MET;STRAND=+;CDS=c.3082+2T>C;AA=p.?;CNT=1 +7 116412046 COSM744044 A G . . GENE=MET;STRAND=+;CDS=c.3082+3A>G;AA=p.?;CNT=1 +7 116417442 COSM598582 G T . . GENE=MET;STRAND=+;CDS=c.3314-1G>T;AA=p.?;CNT=1 +7 116417470 COSM744042 C G . . GENE=MET;STRAND=+;CDS=c.3341C>G;AA=p.T1114S;CNT=1 +7 116417479 COSM201908 A G . . GENE=MET;STRAND=+;CDS=c.3350A>G;AA=p.D1117G;CNT=1 +7 116417499 COSM697 C G . . GENE=MET;STRAND=+;CDS=c.3370C>G;AA=p.H1124D;CNT=1 +7 116417505 COSM1084409 G T . . GENE=MET;STRAND=+;CDS=c.3376G>T;AA=p.A1126S;CNT=1 +7 116423428 COSM598581 T C . . GENE=MET;STRAND=+;CDS=c.3757T>C;AA=p.Y1253H;CNT=1 +7 116423476 COSM1084413 G A . . GENE=MET;STRAND=+;CDS=c.3805G>A;AA=p.A1269T;CNT=1 +7 128845131 COSM744582 G T . . GENE=SMO;STRAND=+;CDS=c.625G>T;AA=p.D209Y;CNT=1 +7 128845134 COSM364081 G A . . GENE=SMO;STRAND=+;CDS=c.628G>A;AA=p.V210M;CNT=1 +7 128845209 COSM484808 G A . . GENE=SMO;STRAND=+;CDS=c.703G>A;AA=p.A235T;CNT=1 +7 128845210 COSM1226876 C T . . GENE=SMO;STRAND=+;CDS=c.704C>T;AA=p.A235V;CNT=1 +7 128845240 COSM248789 C G . . GENE=SMO;STRAND=+;CDS=c.734C>G;AA=p.T245R;CNT=1 +7 128846040 COSM13147 G A . . GENE=SMO;STRAND=+;CDS=c.970G>A;AA=p.A324T;CNT=1 +7 128846155 COSM599001 T G . . GENE=SMO;STRAND=+;CDS=c.1085T>G;AA=p.L362R;CNT=1 +7 128846367 COSM484809 G T . . GENE=SMO;STRAND=+;CDS=c.1203G>T;AA=p.A401A;CNT=2 +7 128846398 COSM216037 C T . . GENE=SMO;STRAND=+;CDS=c.1234C>T;AA=p.L412F;CNT=2 +7 128846405 COSM599000 T C . . GENE=SMO;STRAND=+;CDS=c.1241T>C;AA=p.V414A;CNT=1 +7 128846427 COSM373306 A T . . GENE=SMO;STRAND=+;CDS=c.1263A>T;AA=p.R421R;CNT=1 +7 128850360 COSM1085436 G A . . GENE=SMO;STRAND=+;CDS=c.1623G>A;AA=p.T541T;CNT=1 +7 128850377 COSM598998 G T . . GENE=SMO;STRAND=+;CDS=c.1640G>T;AA=p.R547L;CNT=1 +7 128851599 COSM598997 G T . . GENE=SMO;STRAND=+;CDS=c.1924G>T;AA=p.V642L;CNT=1 +7 140453096 COSM599336 C A . . GENE=BRAF;STRAND=-;CDS=c.1839G>T;AA=p.L613F;CNT=1 +7 140453108 COSM745347 C A . . GENE=BRAF;STRAND=-;CDS=c.1827G>T;AA=p.Q609H;CNT=1 +7 140453132 COSM6265 T A . . GENE=BRAF;STRAND=-;CDS=c.1803A>T;AA=p.K601N;CNT=2 +7 140453134 COSM478 T C . . GENE=BRAF;STRAND=-;CDS=c.1801A>G;AA=p.K601E;CNT=5 +7 140453134 COSM475 TCA TTT . . GENE=BRAF;STRAND=-;CDS=c.1799_1800TG>AA;AA=p.V600E;CNT=1 +7 140453136 COSM476 A T . . GENE=BRAF;STRAND=-;CDS=c.1799T>A;AA=p.V600E;CNT=127 +7 140453145 COSM471 A C . . GENE=BRAF;STRAND=-;CDS=c.1790T>G;AA=p.L597R;CNT=2 +7 140453154 COSM467 T C . . GENE=BRAF;STRAND=-;CDS=c.1781A>G;AA=p.D594G;CNT=1 +7 140453155 COSM144576 C G . . GENE=BRAF;STRAND=-;CDS=c.1780G>C;AA=p.D594H;CNT=1 +7 140453155 COSM27639 C T . . GENE=BRAF;STRAND=-;CDS=c.1780G>A;AA=p.D594N;CNT=1 +7 140453158 COSM231846 C T . . GENE=BRAF;STRAND=-;CDS=c.1777G>A;AA=p.G593S;CNT=1 +7 140453193 COSM462 T C . . GENE=BRAF;STRAND=-;CDS=c.1742A>G;AA=p.N581S;CNT=4 +7 140481397 COSM1158381 C T . . GENE=BRAF;STRAND=-;CDS=c.1411G>A;AA=p.V471I;CNT=1 +7 140481401 COSM347662 TCC TAG . . GENE=BRAF;STRAND=-;CDS=c.1405_1406GG>CT;AA=p.G469>?;CNT=1 +7 140481402 COSM459 C A . . GENE=BRAF;STRAND=-;CDS=c.1406G>T;AA=p.G469V;CNT=3 +7 140481403 COSM457 C T . . GENE=BRAF;STRAND=-;CDS=c.1405G>A;AA=p.G469R;CNT=2 +7 140481408 COSM27911 G A . . GENE=BRAF;STRAND=-;CDS=c.1400C>T;AA=p.S467L;CNT=1 +7 140481411 COSM453 C T . . GENE=BRAF;STRAND=-;CDS=c.1397G>A;AA=p.G466E;CNT=2 +7 140481411 COSM451 C A . . GENE=BRAF;STRAND=-;CDS=c.1397G>T;AA=p.G466V;CNT=3 +7 140481417 COSM450 C A . . GENE=BRAF;STRAND=-;CDS=c.1391G>T;AA=p.G464V;CNT=1 +7 140481423 COSM1086264 C T . . GENE=BRAF;STRAND=-;CDS=c.1385G>A;AA=p.R462K;CNT=1 +7 140481459 COSM378503 C A . . GENE=BRAF;STRAND=-;CDS=c.1349G>T;AA=p.W450L;CNT=1 +8 38282201 COSM334850 C A . . GENE=Q7Z2S2_HUMAN;STRAND=-;CDS=c.762G>T;AA=p.R254R;CNT=1 +8 38282201 COSM334853 C A . . GENE=FGFR1_ENST00000447712;STRAND=-;CDS=c.762G>T;AA=p.R254R;CNT=1 +8 38282201 COSM334852 C A . . GENE=FGFR1;STRAND=-;CDS=c.762G>T;AA=p.R254R;CNT=1 +8 38282201 COSM334851 C A . . GENE=FGFR1_ENST00000425967;STRAND=-;CDS=c.495G>T;AA=p.R165R;CNT=1 +8 38285938 COSM601 G A . . GENE=FGFR1;STRAND=-;CDS=c.374C>T;AA=p.S125L;CNT=1 +9 21971123 COSM13974 T TT . . GENE=CDKN2A;STRAND=-;CDS=c.234_235insA;AA=p.T79fs*41;CNT=1 +9 21971123 COSM1191044 T TT . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.234_235insA;AA=p.T79fs*41;CNT=1 +9 21971123 COSM1191043 T TT . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.400_401insA;AA=p.H134fs*>41;CNT=1 +9 21971123 COSM12518 TGA T . . GENE=CDKN2A;STRAND=-;CDS=c.233_234delTC;AA=p.L78fs*41;CNT=1 +9 21971123 COSM128615 TGA T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.399_400delTC;AA=p.H134fs*>40;CNT=1 +9 21971123 COSM128616 TGA T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.233_234delTC;AA=p.L78fs*41;CNT=1 +9 21971132 COSM13712 C T . . GENE=CDKN2A;STRAND=-;CDS=c.226G>A;AA=p.A76T;CNT=1 +9 21971132 COSM1200602 C T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.226G>A;AA=p.A76T;CNT=1 +9 21971132 COSM1200601 C T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.392G>A;AA=p.R131H;CNT=1 +9 21971140 COSM608438 G T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.384C>A;AA=p.R128R;CNT=1 +9 21971140 COSM608440 G T . . GENE=CDKN2A;STRAND=-;CDS=c.218C>A;AA=p.A73D;CNT=1 +9 21971140 COSM608439 G T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.218C>A;AA=p.A73D;CNT=1 +9 21971146 COSM85564 TTGGGCTCCGCGCCGTGGAGCAGCAG T . . GENE=CDKN2A;STRAND=-;CDS=c.187_211del25;AA=p.L63fs*75;CNT=1 +9 21971150 COSM85563 GCTCCGCGCCGTGGAGCAGCAGCAGCT G . . GENE=CDKN2A;STRAND=-;CDS=c.182_207del26;AA=p.E61fs*50;CNT=1 +9 21971153 COSM13592 CCG C . . GENE=CDKN2A;STRAND=-;CDS=c.203_204delCG;AA=p.A68fs*51;CNT=2 +9 21971153 COSM1167575 CCG C . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.369_370delCG;AA=p.G124fs*>50;CNT=1 +9 21971153 COSM1167576 CCG C . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.203_204delCG;AA=p.A68fs*51;CNT=1 +9 21971153 COSM41693 CCG C . . GENE=CDKN2a(p14);STRAND=-;CDS=c.369_370delCG;AA=p.G124fs*51;CNT=1 +9 21971158 COSM1107902 C T . . GENE=CDKN2A;STRAND=-;CDS=c.200G>A;AA=p.G67D;CNT=1 +9 21971158 COSM1107901 C T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.200G>A;AA=p.G67D;CNT=1 +9 21971158 COSM1107900 C T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.366G>A;AA=p.R122R;CNT=1 +9 21971185 COSM12731 CGG CAA . . GENE=CDKN2A;STRAND=-;CDS=c.171_172CC>TT;AA=p.R58*;CNT=1 +9 21971185 COSM142989 CGG CAA . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.337_338CC>TT;AA=p.P113L;CNT=1 +9 21971185 COSM142990 CGG CAA . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.171_172CC>TT;AA=p.R58*;CNT=1 +9 21971185 COSM231506 CG C . . GENE=CDKN2A;STRAND=-;CDS=c.172delC;AA=p.R58fs*88;CNT=2 +9 21971185 COSM231507 CG C . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.338delC;AA=p.P113fs*>61;CNT=2 +9 21971185 COSM231508 CG C . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.172delC;AA=p.R58fs*88;CNT=2 +9 21971186 COSM99731 G A . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.172C>T;AA=p.R58*;CNT=3 +9 21971186 COSM12473 G A . . GENE=CDKN2A;STRAND=-;CDS=c.172C>T;AA=p.R58*;CNT=3 +9 21971186 COSM99730 G A . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.338C>T;AA=p.P113L;CNT=3 +9 21971189 COSM310018 C T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.335G>A;AA=p.R112H;CNT=1 +9 21971189 COSM310017 C T . . GENE=CDKN2A;STRAND=-;CDS=c.169G>A;AA=p.A57T;CNT=1 +9 21971189 COSM310019 C T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.169G>A;AA=p.A57T;CNT=1 +9 21971189 COSM110663 C CC . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.334_335insG;AA=p.S114fs*>61;CNT=1 +9 21971189 COSM110662 C CC . . GENE=CDKN2A;STRAND=-;CDS=c.168_169insG;AA=p.A57fs*63;CNT=1 +9 21971189 COSM110664 C CC . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.168_169insG;AA=p.A57fs*63;CNT=1 +9 21971199 COSM753727 C G . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.325G>C;AA=p.D109H;CNT=1 +9 21971199 COSM753729 C G . . GENE=CDKN2A;STRAND=-;CDS=c.159G>C;AA=p.M53I;CNT=1 +9 21971199 COSM753728 C G . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.159G>C;AA=p.M53I;CNT=1 +9 21971203 COSM608435 A C . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.321T>G;AA=p.H107Q;CNT=2 +9 21971203 COSM608436 A C . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.155T>G;AA=p.M52R;CNT=2 +9 21971203 COSM608437 A C . . GENE=CDKN2A;STRAND=-;CDS=c.155T>G;AA=p.M52R;CNT=2 +9 21971203 COSM1173508 A AA . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.154_155insT;AA=p.M52fs*68;CNT=1 +9 21971203 COSM1173507 A AA . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.320_321insT;AA=p.D108fs*1;CNT=1 +9 21971203 COSM1173509 A AA . . GENE=CDKN2A;STRAND=-;CDS=c.154_155insT;AA=p.M52fs*68;CNT=1 +9 21971208 COSM363012 C A . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.317-1G>T;AA=p.?;CNT=1 +9 21971208 COSM127094 C T . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.317-1G>A;AA=p.?;CNT=1 +9 21971208 COSM13223 C T . . GENE=CDKN2A;STRAND=-;CDS=c.151-1G>A;AA=p.?;CNT=1 +9 21971208 COSM363013 C A . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.151-1G>T;AA=p.?;CNT=1 +9 21971208 COSM127095 C T . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.151-1G>A;AA=p.?;CNT=1 +9 21971208 COSM12537 C A . . GENE=CDKN2A;STRAND=-;CDS=c.151-1G>T;AA=p.?;CNT=1 +9 21971209 COSM608433 T A . . GENE=CDKN2A_ENST00000361570;STRAND=-;CDS=c.317-2A>T;AA=p.?;CNT=1 +9 21971209 COSM13222 T A . . GENE=CDKN2A;STRAND=-;CDS=c.151-2A>T;AA=p.?;CNT=1 +9 21971209 COSM608434 T A . . GENE=CDKN2A_ENST00000446177;STRAND=-;CDS=c.151-2A>T;AA=p.?;CNT=1 +9 80336317 COSM1110323 G A . . GENE=GNAQ;STRAND=-;CDS=c.1002C>T;AA=p.T334T;CNT=1 +9 80336345 COSM123394 T A . . GENE=GNAQ;STRAND=-;CDS=c.974A>T;AA=p.Y325F;CNT=1 +9 80336376 COSM384149 C T . . GENE=GNAQ;STRAND=-;CDS=c.943G>A;AA=p.D315N;CNT=1 +9 80336400 COSM170856 C A . . GENE=GNAQ;STRAND=-;CDS=c.919G>T;AA=p.E307*;CNT=1 +9 80343574 COSM77782 C T . . GENE=GNAQ;STRAND=-;CDS=c.745G>A;AA=p.E249K;CNT=1 +9 80343579 COSM354690 C A . . GENE=GNAQ;STRAND=-;CDS=c.740G>T;AA=p.R247L;CNT=1 +9 80409421 COSM1110325 C T . . GENE=GNAQ;STRAND=-;CDS=c.693G>A;AA=p.A231A;CNT=1 +9 80409502 COSM1110326 G A . . GENE=GNAQ;STRAND=-;CDS=c.612C>T;AA=p.V204V;CNT=1 +9 80412494 COSM281411 G A . . GENE=GNAQ;STRAND=-;CDS=c.547C>T;AA=p.R183*;CNT=1 +9 80412499 COSM292645 C G . . GENE=GNAQ;STRAND=-;CDS=c.542G>C;AA=p.R181T;CNT=1 +9 133738351 COSM383613 G T . . GENE=ABL1;STRAND=+;CDS=c.751G>T;AA=p.G251C;CNT=1 +9 133748333 COSM1176546 C T . . GENE=ABL1;STRAND=+;CDS=c.994C>T;AA=p.R332W;CNT=1 +9 133750337 COSM1181443 G T . . GENE=ABL1;STRAND=+;CDS=c.1168G>T;AA=p.G390W;CNT=2 +9 133750392 COSM364137 C T . . GENE=ABL1;STRAND=+;CDS=c.1223C>T;AA=p.P408L;CNT=1 +9 139397773 COSM462420 G A . . GENE=NOTCH1_ENST00000277541;STRAND=-;CDS=c.5028C>T;AA=p.V1676V;CNT=1 +9 139397773 COSM462421 G A . . GENE=NOTCH1;STRAND=-;CDS=c.5028C>T;AA=p.V1676V;CNT=1 +9 139399350 COSM13053 C G . . GENE=NOTCH1;STRAND=-;CDS=c.4793G>C;AA=p.R1598P;CNT=1 +9 139399350 COSM305943 C G . . GENE=NOTCH1_ENST00000277541;STRAND=-;CDS=c.4793G>C;AA=p.R1598P;CNT=1 +9 139399362 COSM136758 C T . . GENE=NOTCH1_ENST00000277541;STRAND=-;CDS=c.4781G>A;AA=p.R1594Q;CNT=1 +9 139399362 COSM136759 C T . . GENE=NOTCH1;STRAND=-;CDS=c.4781G>A;AA=p.R1594Q;CNT=1
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/filters/CosmicNonCodingVariants_v64_26032013_noLimit_wgs.f.vcf Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,52 @@ +##fileformat=VCFv4.1 +##source=COSMICv64 +##reference=GRCh37 +##fileDate=20130327 +##comment="Missing nucleotide details indicate ambiguity during curation process" +##comment="URL stub for COSM ID field='http://www.sanger.ac.uk/cgi-bin/genetics/CGP/directive?id='" +##comment="REF and ALT sequences are both forward strand +##INFO=<ID=GENE,Number=1,Type=String,Description="Gene name"> +##INFO=<ID=STRAND,Number=1,Type=String,Description="Gene strand"> +##INFO=<ID=CDS,Number=1,Type=String,Description="CDS annotation"> +##INFO=<ID=AA,Number=1,Type=String,Description="Peptide annotation"> +##INFO=<ID=CNT,Number=1,Type=Integer,Description="How many samples have this mutation"> +#CHROM POS ID REF ALT QUAL FILTER INFO +1 115258837 COSN414678 C A . . . +1 115258837 COSN414677 C A . . . +1 115258839 COSN414680 T C . . . +1 115258839 COSN414679 T C . . . +10 43613962 COSN424480 C A . . GENE=RET;STRAND=+ +10 43617488 COSN424483 G T . . GENE=RET;STRAND=+ +10 89720899 COSN425590 G T . . GENE=PTEN;STRAND=+ +13 48955592 COSN215086 A C . . GENE=RB1;STRAND=+ +13 49027259 COSN434910 A G . . GENE=RB1_ENST00000267163;STRAND=+ +17 7578359 COSN504283 C T . . GENE=TP53;STRAND=- +19 3118848 COSN449010 T G . . GENE=GNA11;STRAND=+ +19 3121198 COSN498712 G A . . . +2 132181403 COSN452344 G C . . . +2 212589935 COSN214321 A G . . GENE=ERBB4;STRAND=- +22 17052984 COSN460731 A G . . . +22 17055427 COSN166685 G T . . . +22 24143286 COSN169414 C T . . GENE=SMARCB1;STRAND=+ +4 55593344 COSN467850 C A . . GENE=KIT;STRAND=+ +4 55593517 COSN467851 G C . . GENE=KIT;STRAND=+ +4 55599403 COSN467856 G T . . GENE=KIT;STRAND=+ +4 55973071 COSN467867 T A . . GENE=KDR;STRAND=- +4 55980471 COSN167219 C A . . GENE=KDR;STRAND=- +5 149453163 COSN470115 C A . . GENE=CSF1R;STRAND=- +5 149453163 COSN470116 C A . . GENE=CSF1R;STRAND=- +7 55211207 COSN479937 G C . . GENE=EGFR;STRAND=+ +7 65970233 COSN480663 G T . . . +7 65970320 COSN480664 G A . . . +7 65970329 COSN480666 G T . . . +7 65970329 COSN480665 G T . . . +7 116340357 COSN476961 C A . . GENE=MET;STRAND=+ +7 128851663 COSN477274 G A . . GENE=SMO;STRAND=+ +9 33675634 COSN486051 G T . . . +9 33675675 COSN232514 A N . . . +9 33675970 COSN232057 G N . . . +9 33676082 COSN486052 G A . . . +9 33676271 COSN486053 C T . . . +9 33676373 COSN486054 G T . . . +9 33676393 COSN486055 G A . . . +9 80336213 COSN502865 G A . . .
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/filters/README Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,1 @@ +Filters are made from dbSNP, both clinical and with no known medical impact and from cosmic, both coding and non-coding. Only chromocol coordinates are recorded in the file.
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/falco/ref/filters/clinvar_00-latest.f.vcf Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,593 @@ +##fileformat=VCFv4.0 +##fileStatus=!!!! This is a provisional file !!!! +##fileDate=20121105 +##source=dbSNP +##dbSNP_BUILD_ID=137 +##reference=GRCh37.p5 +##phasing=partial +##variationPropertyDocumentationUrl=ftp://ftp.ncbi.nlm.nih.gov/snp/specs/dbSNP_BitField_latest.pdf +##INFO=<ID=RSPOS,Number=1,Type=Integer,Description="Chr position reported in dbSNP"> +##INFO=<ID=RV,Number=0,Type=Flag,Description="RS orientation is reversed"> +##INFO=<ID=VP,Number=1,Type=String,Description="Variation Property. Documentation is at ftp://ftp.ncbi.nlm.nih.gov/snp/specs/dbSNP_BitField_latest.pdf"> +##INFO=<ID=GENEINFO,Number=1,Type=String,Description="Pairs each of gene symbol:gene id. The gene symbol and id are delimited by a colon (:) and each pair is delimited by a vertical bar (|)"> +##INFO=<ID=dbSNPBuildID,Number=1,Type=Integer,Description="First dbSNP Build for RS"> +##INFO=<ID=SAO,Number=1,Type=Integer,Description="Variant Allele Origin: 0 - unspecified, 1 - Germline, 2 - Somatic, 3 - Both"> +##INFO=<ID=SSR,Number=1,Type=Integer,Description="Variant Suspect Reason Codes (may be more than one value added together) 0 - unspecified, 1 - Paralog, 2 - byEST, 4 - oldAlign, 8 - Para_EST, 16 - 1kg_failed, 1024 - other"> +##INFO=<ID=GMAF,Number=1,Type=Float,Description="Global Minor Allele Frequency [0, 0.5]; global population is 1000GenomesProject phase 1 genotype data from 629 individuals, released in the 11-23-2010 dataset"> +##INFO=<ID=WGT,Number=1,Type=Integer,Description="Weight, 00 - unmapped, 1 - weight 1, 2 - weight 2, 3 - weight 3 or more"> +##INFO=<ID=VC,Number=1,Type=String,Description="Variation Class"> +##INFO=<ID=PM,Number=0,Type=Flag,Description="Variant is Precious(Clinical,Pubmed Cited)"> +##INFO=<ID=TPA,Number=0,Type=Flag,Description="Provisional Third Party Annotation(TPA) (currently rs from PHARMGKB who will give phenotype data)"> +##INFO=<ID=PMC,Number=0,Type=Flag,Description="Links exist to PubMed Central article"> +##INFO=<ID=S3D,Number=0,Type=Flag,Description="Has 3D structure - SNP3D table"> +##INFO=<ID=SLO,Number=0,Type=Flag,Description="Has SubmitterLinkOut - From SNP->SubSNP->Batch.link_out"> +##INFO=<ID=NSF,Number=0,Type=Flag,Description="Has non-synonymous frameshift A coding region variation where one allele in the set changes all downstream amino acids. FxnClass = 44"> +##INFO=<ID=NSM,Number=0,Type=Flag,Description="Has non-synonymous missense A coding region variation where one allele in the set changes protein peptide. FxnClass = 42"> +##INFO=<ID=NSN,Number=0,Type=Flag,Description="Has non-synonymous nonsense A coding region variation where one allele in the set changes to STOP codon (TER). FxnClass = 41"> +##INFO=<ID=REF,Number=0,Type=Flag,Description="Has reference A coding region variation where one allele in the set is identical to the reference sequence. FxnCode = 8"> +##INFO=<ID=SYN,Number=0,Type=Flag,Description="Has synonymous A coding region variation where one allele in the set does not change the encoded amino acid. FxnCode = 3"> +##INFO=<ID=U3,Number=0,Type=Flag,Description="In 3' UTR Location is in an untranslated region (UTR). FxnCode = 53"> +##INFO=<ID=U5,Number=0,Type=Flag,Description="In 5' UTR Location is in an untranslated region (UTR). FxnCode = 55"> +##INFO=<ID=ASS,Number=0,Type=Flag,Description="In acceptor splice site FxnCode = 73"> +##INFO=<ID=DSS,Number=0,Type=Flag,Description="In donor splice-site FxnCode = 75"> +##INFO=<ID=INT,Number=0,Type=Flag,Description="In Intron FxnCode = 6"> +##INFO=<ID=R3,Number=0,Type=Flag,Description="In 3' gene region FxnCode = 13"> +##INFO=<ID=R5,Number=0,Type=Flag,Description="In 5' gene region FxnCode = 15"> +##INFO=<ID=OTH,Number=0,Type=Flag,Description="Has other variant with exactly the same set of mapped positions on NCBI refernce assembly."> +##INFO=<ID=CFL,Number=0,Type=Flag,Description="Has Assembly conflict. This is for weight 1 and 2 variant that maps to different chromosomes on different assemblies."> +##INFO=<ID=ASP,Number=0,Type=Flag,Description="Is Assembly specific. This is set if the variant only maps to one assembly"> +##INFO=<ID=MUT,Number=0,Type=Flag,Description="Is mutation (journal citation, explicit fact): a low frequency variation that is cited in journal and other reputable sources"> +##INFO=<ID=VLD,Number=0,Type=Flag,Description="Is Validated. This bit is set if the variant has 2+ minor allele count based on frequency or genotype data."> +##INFO=<ID=G5A,Number=0,Type=Flag,Description=">5% minor allele frequency in each and all populations"> +##INFO=<ID=G5,Number=0,Type=Flag,Description=">5% minor allele frequency in 1+ populations"> +##INFO=<ID=HD,Number=0,Type=Flag,Description="Marker is on high density genotyping kit (50K density or greater). The variant may have phenotype associations present in dbGaP."> +##INFO=<ID=GNO,Number=0,Type=Flag,Description="Genotypes available. The variant has individual genotype (in SubInd table)."> +##INFO=<ID=KGValidated,Number=0,Type=Flag,Description="1000 Genome validated"> +##INFO=<ID=KGPhase1,Number=0,Type=Flag,Description="1000 Genome phase 1 (incl. June Interim phase 1)"> +##INFO=<ID=KGPilot123,Number=0,Type=Flag,Description="1000 Genome discovery all pilots 2010(1,2,3)"> +##INFO=<ID=KGPROD,Number=0,Type=Flag,Description="Has 1000 Genome submission"> +##INFO=<ID=OTHERKG,Number=0,Type=Flag,Description="non-1000 Genome submission"> +##INFO=<ID=PH3,Number=0,Type=Flag,Description="HAP_MAP Phase 3 genotyped: filtered, non-redundant"> +##INFO=<ID=CDA,Number=0,Type=Flag,Description="Variation is interrogated in a clinical diagnostic assay"> +##INFO=<ID=LSD,Number=0,Type=Flag,Description="Submitted from a locus-specific database"> +##INFO=<ID=MTP,Number=0,Type=Flag,Description="Microattribution/third-party annotation(TPA:GWAS,PAGE)"> +##INFO=<ID=OM,Number=0,Type=Flag,Description="Has OMIM/OMIA"> +##INFO=<ID=NOC,Number=0,Type=Flag,Description="Contig allele not present in variant allele list. The reference sequence allele at the mapped position is not present in the variant allele list, adjusted for orientation."> +##INFO=<ID=WTD,Number=0,Type=Flag,Description="Is Withdrawn by submitter If one member ss is withdrawn by submitter, then this bit is set. If all member ss' are withdrawn, then the rs is deleted to SNPHistory"> +##INFO=<ID=NOV,Number=0,Type=Flag,Description="Rs cluster has non-overlapping allele sets. True when rs set has more than 2 alleles from different submissions and these sets share no alleles in common."> +##INFO=<ID=GCF,Number=0,Type=Flag,Description="Has Genotype Conflict Same (rs, ind), different genotype. N/N is not included."> +##FILTER=<ID=NC,Description="Inconsistent Genotype Submission For At Least One Sample"> +##INFO=<ID=CLNHGVS,Number=.,Type=String,Description="Variant names from HGVS. The order of these variants corresponds to the order of the info in the other clinical INFO tags."> +##INFO=<ID=CLNALLE,Number=.,Type=Integer,Description="Variant alleles from REF or ALT columns. 0 is REF, 1 is the first ALT allele, etc. This is used to match alleles with other corresponding clinical (CLN) INFO tags. A value of -1 indicates that no allele was found to match a corresponding HGVS allele name."> +##INFO=<ID=CLNSRC,Number=.,Type=String,Description="Variant Clinical Chanels"> +##INFO=<ID=CLNORIGIN,Number=.,Type=String,Description="Allele Origin. One or more of the following values may be added: 0 - unknown; 1 - germline; 2 - somatic; 4 - inherited; 8 - paternal; 16 - maternal; 32 - de-novo; 64 - biparental; 128 - uniparental; 256 - not-tested; 512 - tested-inconclusive; 1073741824 - other"> +##INFO=<ID=CLNSRCID,Number=.,Type=String,Description="Variant Clinical Channel IDs"> +##INFO=<ID=CLNSIG,Number=.,Type=String,Description="Variant Clinical Significance, 0 - unknown, 1 - untested, 2 - non-pathogenic, 3 - probable-non-pathogenic, 4 - probable-pathogenic, 5 - pathogenic, 6 - drug-response, 7 - histocompatibility, 255 - other"> +##INFO=<ID=CLNDSDB,Number=.,Type=String,Description="Variant disease database name"> +##INFO=<ID=CLNDSDBID,Number=.,Type=String,Description="Variant disease database ID"> +##INFO=<ID=CLNDBN,Number=.,Type=String,Description="Variant disease name"> +##INFO=<ID=CLNACC,Number=.,Type=String,Description="Variant Accession and Versions"> +#CHROM POS ID REF ALT QUAL FILTER INFO +1 43815007 rs121913616 GTG GAA . . RSPOS=43815008;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110800;GENEINFO=MPL:4352;WGT=1;VC=MNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000001.10:g.43815008_43815009delinsAA;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=159530.0012;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Myelofibrosis with myeloid metaplasia\x2c somatic;CLNACC=RCV000015228.1 +1 43815009 rs121913615 G T . . RSPOS=43815009;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=MPL:4352;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000001.10:g.43815009G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=159530.0011;CLNSIG=255|255;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Myelofibrosis with myeloid metaplasia\x2c somatic|THROMBOCYTHEMIA 2\x2c SOMATIC;CLNACC=RCV000015227.1|RCV000022668.1 +1 115256528 rs121913255 T A . . RSPOS=115256528;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000001.10:g.115256528T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +1 115256529 rs11554290 T A,C,G . . RSPOS=115256529;RV;dbSNPBuildID=120;SSR=0;SAO=3;VP=050360000a01000103110124;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;PH3;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000001.10:g.115256529T>A,NC_000001.10:g.115256529T>C,NC_000001.10:g.115256529T>G;CLNSRC=.,OMIM Allelic Variant,.;CLNORIGIN=2,1,2;CLNSRCID=.,164790.0002,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,Thyroid carcinoma\x2c follicular\x2c somatic,.;CLNACC=.,RCV000014914.1,. +1 115256532 rs267606920 C T . . RSPOS=115256532;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000001.10:g.115256532C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=164790.0005;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C2750732:613224:648;CLNDBN=Noonan syndrome 6;CLNACC=RCV000014917.1 +1 115256562 rs267606921 G A . . RSPOS=115256562;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000001.10:g.115256562G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=164790.0004;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C2750732:613224:648;CLNDBN=Noonan syndrome 6;CLNACC=RCV000014916.1 +1 115258730 rs121913248 C G,T . . RSPOS=115258730;RV;GMAF=0.0005;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000016100120;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=2;CLNHGVS=NC_000001.10:g.115258730C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +1 115258744 rs121434596 C A,G,T . . RSPOS=115258744;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000001.10:g.115258744C>A,NC_000001.10:g.115258744C>G,NC_000001.10:g.115258744C>T;CLNSRC=.,.,OMIM Allelic Variant;CLNORIGIN=2,2,2;CLNSRCID=.,.,164790.0003;CLNSIG=255,255,5|5|5;CLNDSDB=.,.,NCBI:OMIM:Orphanet|NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=.,.,CN069957:614470:3261|C0349639:607785:86834|NBK1124:C2750732:613224:648;CLNDBN=.,.,AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME\x2c TYPE IV|Juvenile myelomonocytic leukemia|Noonan syndrome 6;CLNACC=.,.,RCV000014915.1|RCV000022689.1|RCV000022690.1 +1 115258745 rs121434595 C A,G,T . . RSPOS=115258745;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000001.10:g.115258745C>A,NC_000001.10:g.115258745C>G,NC_000001.10:g.115258745C>T;CLNSRC=.,OMIM Allelic Variant,.;CLNORIGIN=2,2,2;CLNSRCID=.,164790.0001,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,Rectal cancer\x2c somatic,.;CLNACC=.,RCV000014913.1,. +1 115258747 rs121913237 C A,G,T . . RSPOS=115258747;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100124;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000001.10:g.115258747C>A,NC_000001.10:g.115258747C>G,NC_000001.10:g.115258747C>T;CLNSRC=.,.,.;CLNORIGIN=2,2,2;CLNSRCID=.,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +1 115258748 rs121913250 C A,G,T . . RSPOS=115258748;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100124;GENEINFO=NRAS:4893;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000001.10:g.115258748C>A,NC_000001.10:g.115258748C>G,NC_000001.10:g.115258748C>T;CLNSRC=.,.,.;CLNORIGIN=2,2,2;CLNSRCID=.,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +2 29432664 rs113994087 C T . . RSPOS=29432664;RV;dbSNPBuildID=132;SSR=0;SAO=1;VP=050360000a01000002110100;GENEINFO=ALK:238;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000002.11:g.29432664C>T;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=NBK24599|105590.0001;CLNSIG=255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK24599:C2751681:613014:635;CLNDBN=Neuroblastoma 3;CLNACC=RCV000019709.1 +2 29432739 rs113994092 A G . . RSPOS=29432739;RV;dbSNPBuildID=132;SSR=0;SAO=0;VP=050360000a01000002110100;GENEINFO=ALK:238;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000002.11:g.29432739A>G;CLNSRC=GeneReviews;CLNORIGIN=.;CLNSRCID=NBK24599;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK24599:C2751681:613014:635;CLNDBN=Neuroblastoma 3;CLNACC=RCV000021080.1 +2 29443697 rs281864719 A C . . RSPOS=29443697;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050160000a01000002110100;WGT=1;VC=SNV;PM;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000002.11:g.29443697A>C;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +2 209113112 rs121913500 C T . . RSPOS=209113112;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=IDH1:3417;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000002.11:g.209113112C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +2 209113113 rs121913499 G A,T . . RSPOS=209113113;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=IDH1:3417;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000002.11:g.209113113G>A,NC_000002.11:g.209113113G>T;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +2 212288940 rs147624110 C T . . RSPOS=212288940;dbSNPBuildID=134;SSR=0;SAO=3;VP=050068000a01000002100120;GENEINFO=ERBB4:2066;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000002.11:g.212288940C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +2 212576877 rs148183215 G A . . RSPOS=212576877;dbSNPBuildID=134;SSR=0;SAO=3;VP=050268000a01000002100120;GENEINFO=ERBB4:2066;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000002.11:g.212576877G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10183773 rs193922608 C T . . RSPOS=10183773;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268000a01000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183773C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10183781 rs5030827 G T . . RSPOS=10183781;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183781G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0025;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome;CLNACC=RCV000002324.1 +3 10183785 rs5030828 T C . . RSPOS=10183785;dbSNPBuildID=113;SSR=0;SAO=3;VP=050360000a01000102100120;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183785T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10183794 rs119103277 G C . . RSPOS=10183794;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183794G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0007;CLNSIG=5|5;CLNDSDB=.|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=.|NBK1463:C0019562:193300:892:46659004;CLNDBN=Hemangioblastoma\x2c sporadic cerebellar|Von Hippel-Lindau syndrome;CLNACC=RCV000002305.1|RCV000002306.1 +3 10183797 rs5030807 T A,C . . RSPOS=10183797;dbSNPBuildID=113;SSR=0;SAO=3;VP=050360000a01000102100120;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183797T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10183808 rs5030808 G A,C . . RSPOS=10183808;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183808G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0026;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1548:C0031511:171300:29072;CLNDBN=Pheochromocytoma;CLNACC=RCV000002325.1 +3 10183823 rs5030809 T C . . RSPOS=10183823;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183823T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0009;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome;CLNACC=RCV000002309.1 +3 10183851 rs193922609 G C . . RSPOS=10183851;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268000a01000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183851G>C;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10183865 rs104893824 T A,C . . RSPOS=10183865;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.10183865T>A,NC_000003.11:g.10183865T>C;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=608537.0017,608537.0012;CLNSIG=5,5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004,NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome,Von Hippel-Lindau syndrome;CLNACC=RCV000002316.1,RCV000002308.1 +3 10183876 rs61758376 G C . . RSPOS=10183876;GMAF=0.0073;dbSNPBuildID=129;SSR=0;SAO=1;VP=050068080001000016100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;INT;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10183876G>C;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10188228 rs193922610 C T . . RSPOS=10188228;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268080a01000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;INT;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10188228C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10188245 rs104893830 G C . . RSPOS=10188245;dbSNPBuildID=132;SSR=0;SAO=1;VP=050268080a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10188245G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0021;CLNSIG=5|5;CLNDSDB=NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C1837915:263400:238557|NBK1463:C0019562:193300:892:46659004;CLNDBN=Erythrocytosis\x2c familial\x2c 2|Von Hippel-Lindau syndrome;CLNACC=RCV000002317.1|RCV000030586.1 +3 10188262 rs119103278 A C . . RSPOS=10188262;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260080a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10188262A>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0008;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hemangioblastoma\x2c sporadic cerebellar;CLNACC=RCV000002307.1 +3 10188315 rs193922611 T A . . RSPOS=10188315;dbSNPBuildID=136;SSR=0;SAO=1;VP=050260080a01000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;INT;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10188315T>A;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191480 rs121913346 T A . . RSPOS=10191480;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191480T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191488 rs5030818 C G,T . . RSPOS=10191488;dbSNPBuildID=113;SSR=0;SAO=3;VP=050368000601000102110120;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;SLO;NSN;REF;GNO;OTHERKG;LSD;OM;CLNALLE=2;CLNHGVS=NC_000003.11:g.10191488C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0006;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome;CLNACC=RCV000002301.1 +3 10191495 rs28940297 T C . . RSPOS=10191495;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191495T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0018;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Renal cell carcinoma with paraneoplastic erythrocytosis;CLNACC=RCV000002319.1 +3 10191498 rs267607170 A G . . RSPOS=10191498;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191498A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=608537.0027;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome;CLNACC=RCV000002326.1 +3 10191506 rs5030820 C G,T . . RSPOS=10191506;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.10191506C>G,NC_000003.11:g.10191506C>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant|OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=608537.0004,608537.0003|608537.0010|608537.0011;CLNSIG=5,5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1463:C0019562:193300:892:46659004,NBK1463:C0019562:193300:892:46659004|NBK1548:C0031511:171300:29072;CLNDBN=Von Hippel-Lindau syndrome,Von Hippel-Lindau syndrome|Pheochromocytoma;CLNACC=RCV000002304.1,RCV000002302.1|RCV000002303.1 +3 10191507 rs5030821 G A . . RSPOS=10191507;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191507G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0005;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1463:C0019562:193300:892:46659004;CLNDBN=Von Hippel-Lindau syndrome;CLNACC=RCV000002300.1 +3 10191531 rs193922613 A G . . RSPOS=10191531;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268000a01000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191531A>G;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191555 rs5030823 C A . . RSPOS=10191555;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000601000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSN;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191555C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0002;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Renal cell carcinoma\x2c somatic;CLNACC=RCV000002299.1 +3 10191556 rs193922614 G A . . RSPOS=10191556;dbSNPBuildID=136;SSR=0;SAO=1;VP=050260000301000002100100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191556G>A;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=3;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191569 rs5030824 C G . . RSPOS=10191569;dbSNPBuildID=113;SSR=0;SAO=1;VP=050360000a01000102110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191569C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0014;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1463:C0019562:193300:892:46659004|C1837915:263400:238557|NBK1548:C0031511:171300:29072;CLNDBN=Von Hippel-Lindau syndrome|Erythrocytosis\x2c familial\x2c 2|Pheochromocytoma;CLNACC=RCV000002311.1|RCV000002312.1|RCV000002313.1 +3 10191572 rs121913345 GA G . . RSPOS=10191574;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060001205000002100220;GENEINFO=VHL:7428;WGT=1;VC=DIV;PM;NSF;REF;ASP;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191574delA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191578 rs28940301 C G . . RSPOS=10191578;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191578C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0024;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C1837915:263400:238557;CLNDBN=Erythrocytosis\x2c familial\x2c 2;CLNACC=RCV000002323.1 +3 10191581 rs28940300 C T . . RSPOS=10191581;dbSNPBuildID=132;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191581C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0023;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C1837915:263400:238557;CLNDBN=Erythrocytosis\x2c familial\x2c 2;CLNACC=RCV000002322.1 +3 10191593 rs281860296 A G . . RSPOS=10191593;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060000a01000002110100;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191593A>G;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 10191605 rs28940298 C T . . RSPOS=10191605;dbSNPBuildID=132;SSR=0;SAO=1;VP=050268000a01000002110100;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191605C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=608537.0019;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C1837915:263400:238557;CLNDBN=Erythrocytosis\x2c familial\x2c 2;CLNACC=RCV000002320.1 +3 10191629 rs121913347 C T . . RSPOS=10191629;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=VHL:7428;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.10191629C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067215 rs63750305 G GAT . . RSPOS=37067217;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=-1;CLNHGVS=NC_000003.11:g.37067216_37067217dupAT;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067217 rs267607824 T C . . RSPOS=37067217;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000301000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067217T>C;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067230 rs63750557 C T . . RSPOS=37067230;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067230C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067237 rs63749965 TG T . . RSPOS=37067239;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067239delG;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067240 rs63750447 T A . . RSPOS=37067240;GMAF=0.0092;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000016100120;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067240T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067242 rs63750760 C T . . RSPOS=37067242;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067242C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067243 rs63750430 G C,T . . RSPOS=37067243;RV;dbSNPBuildID=134;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067243G>C;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067254 rs61751644 C A,T . . RSPOS=37067254;dbSNPBuildID=129;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=2;CLNHGVS=NC_000003.11:g.37067254C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067255 rs63750361 G A,C,T . . RSPOS=37067255;RV;dbSNPBuildID=134;SSR=0;SAO=0;VP=050060000a01040002100104;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;VLD;OTHERKG;LSD;NOV;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067255G>A;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067278 rs63750749 CT C . . RSPOS=37067279;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067279delT;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067281 rs63750483 C T . . RSPOS=37067281;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000601000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067281C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067287 rs63751485 C G . . RSPOS=37067287;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067287C>G;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067298 rs63751015 CCT C . . RSPOS=37067299;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067299_37067300delCT;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067306 rs41294980 G A . . RSPOS=37067306;GMAF=0.0005;dbSNPBuildID=127;SSR=0;SAO=0;VP=050060000a01040016100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;VLD;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067306G>A;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067314 rs63751153 C T . . RSPOS=37067314;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000601000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067314C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067315 rs104895000 A C . . RSPOS=37067315;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067315A>C;CLNSRC=.;CLNORIGIN=0;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067327 rs63750766 C T . . RSPOS=37067327;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067327C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067335 rs267607823 A G . . RSPOS=37067335;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067335A>G;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067340 rs63751118 AGA A . . RSPOS=37067341;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067341_37067342delGA;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067343 rs63751440 T A,G . . RSPOS=37067343;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.37067343T>A,NC_000003.11:g.37067343T>G;CLNSRC=.,.;CLNORIGIN=.,.;CLNSRCID=.,.;CLNSIG=1,1;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +3 37067348 rs63751179 C G . . RSPOS=37067348;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067348C>G;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067349 rs63750293 TA T . . RSPOS=37067350;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=MLH1:4292;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067350delA;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067355 rs63750791 C T . . RSPOS=37067355;RV;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000301000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067355C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067365 rs63750316 C T . . RSPOS=37067365;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000601000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067365C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067386 rs63750443 G C . . RSPOS=37067386;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067386G>C;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 37067393 rs63751414 C T . . RSPOS=37067393;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002100100;GENEINFO=MLH1:4292;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.37067393C>T;CLNSRC=.;CLNORIGIN=.;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266040 rs121913394 G A . . RSPOS=41266040;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266040G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266064 rs121913395 G A . . RSPOS=41266064;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266064G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266068 rs77064436 T C,G . . RSPOS=41266068;dbSNPBuildID=133;SSR=16;SAO=3;VP=050260000a01000402100160;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;HD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266068T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266076 rs121913417 TGGCAGCAACAGTCTTACCTGGACT T . . RSPOS=41266077;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=CTNNB1:1499;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266077_41266100del24;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266097 rs28931588 G A,C,T . . RSPOS=41266097;dbSNPBuildID=132;SSR=0;SAO=3;VP=050268000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266097G>A,NC_000003.11:g.41266097G>C,NC_000003.11:g.41266097G>T;CLNSRC=.,.,OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=2,2,1;CLNSRCID=.,.,116806.0004|116806.0016;CLNSIG=255,255,255|255|255;CLNDSDB=.,.,.|.|.;CLNDSDBID=.,.,.|.|.;CLNDBN=.,.,Hepatoblastoma\x2c somatic|Pilomatricoma\x2c somatic|Pilomatricoma\x2c somatic;CLNACC=.,.,RCV000019144.1|RCV000019145.1|RCV000019155.1 +3 41266098 rs121913396 A C,G,T . . RSPOS=41266098;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266098A>C,NC_000003.11:g.41266098A>G,NC_000003.11:g.41266098A>T;CLNSRC=.,OMIM Allelic Variant,.;CLNORIGIN=2,1,2;CLNSRCID=.,116806.0006,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,Pilomatricoma\x2c somatic,.;CLNACC=.,RCV000019140.1,. +3 41266101 rs121913400 C A,G,T . . RSPOS=41266101;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266101C>A,NC_000003.11:g.41266101C>G,NC_000003.11:g.41266101C>T;CLNSRC=OMIM Allelic Variant,.,OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=1,2,2;CLNSRCID=116806.0002,.,116806.0007|116806.0015;CLNSIG=255|255,255,255|255;CLNDSDB=.|.,.,.|.;CLNDSDBID=.|.,.,.|.;CLNDBN=Colorectal cancer\x2c somatic|Pilomatricoma\x2c somatic,.,Pilomatricoma\x2c somatic|Medulloblastoma\x2c somatic;CLNACC=RCV000019138.1|RCV000019139.1,.,RCV000019147.1|RCV000019148.1 +3 41266103 rs121913399 G A . . RSPOS=41266103;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266103G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 41266104 rs28931589 G A,T . . RSPOS=41266104;dbSNPBuildID=132;SSR=0;SAO=3;VP=050268000a01000002110120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.41266104G>A,NC_000003.11:g.41266104G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,2;CLNSRCID=116806.0008,116806.0005;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=Pilomatricoma\x2c somatic,Hepatoblastoma\x2c somatic;CLNACC=RCV000019149.1,RCV000019146.1 +3 41266112 rs121913228 T C,G . . RSPOS=41266112;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.41266112T>C,NC_000003.11:g.41266112T>G;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +3 41266113 rs121913403 C A,G,T . . RSPOS=41266113;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266113C>A,NC_000003.11:g.41266113C>G,NC_000003.11:g.41266113C>T;CLNSRC=.,OMIM Allelic Variant|OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,1,2;CLNSRCID=.,116806.0009|116806.0012,116806.0010;CLNSIG=255,255|255,255;CLNDSDB=.,.|.,.;CLNDSDBID=.,.|.,.;CLNDBN=.,Ovarian cancer\x2c somatic|Pilomatricoma\x2c somatic,Pilomatricoma\x2c somatic;CLNACC=.,RCV000019141.1|RCV000030945.1,RCV000019151.1 +3 41266124 rs121913412 A C,G,T . . RSPOS=41266124;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266124A>C,NC_000003.11:g.41266124A>G,NC_000003.11:g.41266124A>T;CLNSRC=.,OMIM Allelic Variant,.;CLNORIGIN=2,1,2;CLNSRCID=.,116806.0003,.;CLNSIG=255,255|255,255;CLNDSDB=.,.|NCBI,.;CLNDSDBID=.,.|C2675440,.;CLNDBN=.,Hepatoblastoma\x2c somatic|Desmoid tumor\x2c somatic,.;CLNACC=.,RCV000019142.1|RCV000019143.1,. +3 41266125 rs121913413 C T . . RSPOS=41266125;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.41266125C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=116806.0011;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Pilomatricoma\x2c somatic;CLNACC=RCV000019152.1 +3 41266136 rs121913407 T C,G . . RSPOS=41266136;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.41266136T>C,NC_000003.11:g.41266136T>G;CLNSRC=OMIM Allelic Variant,.;CLNORIGIN=1,2;CLNSRCID=116806.0014,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=Hepatocellular carcinoma\x2c somatic,.;CLNACC=RCV000019154.1,. +3 41266137 rs121913409 C A,G,T . . RSPOS=41266137;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=CTNNB1:1499;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000003.11:g.41266137C>A,NC_000003.11:g.41266137C>G,NC_000003.11:g.41266137C>T;CLNSRC=.,.,OMIM Allelic Variant;CLNORIGIN=2,2,1;CLNSRCID=.,.,116806.0013;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,Hepatocellular carcinoma\x2c somatic;CLNACC=.,.,RCV000019153.1 +3 178916876 rs121913287 G A . . RSPOS=178916876;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178916876G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178921553 rs121913284 T A . . RSPOS=178921553;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178921553T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178927980 rs121913272 T C . . RSPOS=178927980;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178927980T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178936074 rs121913285 C G . . RSPOS=178936074;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936074C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178936082 rs121913273 G A . . RSPOS=178936082;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936082G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178936091 rs104886003 G A . . RSPOS=178936091;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936091G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=171834.0003;CLNSIG=255|255|255|255|255|255;CLNDSDB=.|NCBI|.|.|.|.;CLNDSDBID=.|C0677886|.|.|.|.;CLNDBN=Breast cancer\x2c somatic|Ovarian epithelial cancer|Colorectal cancer\x2c somatic|Gastric cancer\x2c somatic|Nonsmall cell lung cancer\x2c somatic|Keratosis\x2c seborrheic\x2c somatic;CLNACC=RCV000014631.1|RCV000014632.1|RCV000014633.1|RCV000014634.1|RCV000014635.1|RCV000014636.1 +3 178936092 rs121913274 A C,G . . RSPOS=178936092;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.178936092A>C,NC_000003.11:g.178936092A>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=171834.0008,171834.0004;CLNSIG=255,255|255;CLNDSDB=.,.|.;CLNDSDBID=.,.|.;CLNDBN=Hepatocellular carcinoma\x2c somatic,Colorectal cancer\x2c somatic|Nevus\x2c epidermal\x2c somatic;CLNACC=RCV000014643.1,RCV000014637.1|RCV000014638.1 +3 178936093 rs121913275 G T . . RSPOS=178936093;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936093G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178936094 rs121913286 C A,G . . RSPOS=178936094;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.178936094C>A,NC_000003.11:g.178936094C>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=171834.0005,171834.0006;CLNSIG=255|255,255;CLNDSDB=NCBI|.,.;CLNDSDBID=C0677886|.,.;CLNDBN=Ovarian epithelial cancer|Colorectal cancer\x2c somatic,Breast cancer\x2c somatic;CLNACC=RCV000014639.1|RCV000014640.1,RCV000014630.1 +3 178936122 rs104886000 G A . . RSPOS=178936122;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936122G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178936140 rs104886001 G A . . RSPOS=178936140;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060080001000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000003.11:g.178936140G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178938860 rs121913282 A C . . RSPOS=178938860;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178938860A>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178952007 rs121913288 A G . . RSPOS=178952007;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178952007A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178952074 rs121913283 G T . . RSPOS=178952074;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178952074G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178952084 rs121913281 C T . . RSPOS=178952084;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000003.11:g.178952084C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +3 178952085 rs121913279 A G,T . . RSPOS=178952085;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.178952085A>G,NC_000003.11:g.178952085A>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,2;CLNSRCID=171834.0001,171834.0002;CLNSIG=255|255|255|255|255|255|255|1,255;CLNDSDB=.|NCBI|.|.|.|.|.|NCBI:OMIM:Orphanet,.;CLNDSDBID=.|C0677886|.|.|.|.|.|C2752042:612918:140944,.;CLNDBN=Breast cancer\x2c somatic|Ovarian epithelial cancer|Colorectal cancer\x2c somatic|Gastric cancer\x2c somatic|Hepatocellular carcinoma\x2c somatic|Nonsmall cell lung cancer\x2c somatic|Keratosis\x2c seborrheic\x2c somatic|Congenital lipomatous overgrowth\x2c vascular malformations\x2c and epidermal nevi,Breast cancer\x2c somatic;CLNACC=RCV000014622.1|RCV000014623.1|RCV000014624.1|RCV000014625.1|RCV000014626.1|RCV000014627.1|RCV000014628.1|RCV000024621.1,RCV000014629.1 +3 178952090 rs121913277 G A,C . . RSPOS=178952090;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PIK3CA:5290;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000003.11:g.178952090G>A,NC_000003.11:g.178952090G>C;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +4 1803564 rs121913482 C T . . RSPOS=1803564;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803564C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0005;CLNSIG=5|255|5|255|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.|.|.|.;CLNDSDBID=NBK1366:C1868678:187600:85165|.|.|.|.;CLNDBN=Thanatophoric dysplasia type 1|Multiple myeloma\x2c somatic|Skeletal dysplasia with acanthosis nigricans|Nevus\x2c epidermal\x2c somatic|Keratosis\x2c seborrheic\x2c somatic;CLNACC=RCV000017731.1|RCV000017732.1|RCV000017733.1|RCV000017734.1|RCV000017735.1 +4 1803568 rs121913483 C G . . RSPOS=1803568;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803568C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=134934.0013;CLNSIG=5|255|255|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.|.|.;CLNDSDBID=NBK1366:C1868678:187600:85165|.|.|.;CLNDBN=Thanatophoric dysplasia type 1|Cervical cancer\x2c somatic|Bladder cancer\x2c somatic|Keratosis\x2c seborrheic\x2c somatic;CLNACC=RCV000017742.1|RCV000017743.1|RCV000017744.1|RCV000017745.1 +4 1803571 rs4647924 C G . . RSPOS=1803571;dbSNPBuildID=111;SSR=0;SAO=1;VP=050060000a01000502110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;HD;GNO;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803571C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0014;CLNSIG=5|5|5;CLNDSDB=GeneReviews:GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1415:NBK1455:C1864436:602849:53271:440350001|NBK1189:C0175699:101400:794:83015004|.;CLNDBN=Muenke syndrome|Saethre-Chotzen syndrome|Beare-Stevenson syndrome-like anomalies;CLNACC=RCV000017746.1|RCV000017747.1|RCV000017748.1 +4 1803615 rs151254213 G A . . RSPOS=1803615;dbSNPBuildID=134;SSR=0;SAO=3;VP=050068000a01000002100120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803615G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1803655 rs121913115 A G . . RSPOS=1803655;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803655A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0031;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1477:C0410529:146000:429:205468002;CLNDBN=Hypochondroplasia;CLNACC=RCV000017768.1 +4 1803657 rs121913114 A T . . RSPOS=1803657;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1803657A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0030;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1152:C0001080:100800:15:86268005|NBK1477:C0410529:146000:429:205468002;CLNDBN=Achondroplasia|Hypochondroplasia;CLNACC=RCV000017766.1|RCV000017767.1 +4 1806092 rs121913484 A T . . RSPOS=1806092;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1806092A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=134934.0006;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1366:C1868678:187600:85165;CLNDBN=Thanatophoric dysplasia type 1;CLNACC=RCV000017736.1 +4 1806099 rs121913485 A G . . RSPOS=1806099;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1806099A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0016;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1366:C1868678:187600:85165;CLNDBN=Thanatophoric dysplasia type 1;CLNACC=RCV000017751.1 +4 1806104 rs75790268 G T . . RSPOS=1806104;RV;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060080a01000402110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;HD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1806104G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0003;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1152:C0001080:100800:15:86268005;CLNDBN=Achondroplasia;CLNACC=RCV000017727.1 +4 1806111 rs267606809 T G . . RSPOS=1806111;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060080a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1806111T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=134934.0027;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1152:C0001080:100800:15:86268005;CLNDBN=Achondroplasia;CLNACC=RCV000017763.1 +4 1806119 rs28931614 G A,C . . RSPOS=1806119;dbSNPBuildID=132;SSR=0;SAO=0;VP=050060080a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1,2,-1;CLNHGVS=NC_000004.11:g.1806119G>A,NC_000004.11:g.1806119G>C,NC_000004.11:g.1806119G>M;CLNSRC=OMIM Allelic Variant,.,.;CLNORIGIN=.,.,.;CLNSRCID=134934.0001,.,.;CLNSIG=5|1,5,5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|.,.,.;CLNDSDBID=NBK1152:C0001080:100800:15:86268005|.,.,.;CLNDBN=Achondroplasia|Nevus\x2c epidermal\x2c somatic,.,.;CLNACC=RCV000017724.1|RCV000029207.1,.,. +4 1806153 rs28931615 C A . . RSPOS=1806153;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1806153C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0011;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1455:C2677099:612247:93262;CLNDBN=Crouzon syndrome with acanthosis nigricans;CLNACC=RCV000017726.1 +4 1807849 rs104886005 C G . . RSPOS=1807849;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1807849C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1807876 rs104886006 C T . . RSPOS=1807876;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000301000002100120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1807876C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1807889 rs78311289 A C,G . . RSPOS=1807889;dbSNPBuildID=131;SSR=0;SAO=3;VP=050260000a01000402110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;HD;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000004.11:g.1807889A>C,NC_000004.11:g.1807889A>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=134934.0022,134934.0004;CLNSIG=5,5|255|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,GeneReviews:NCBI:OMIM:SNOMED CT|.|.;CLNDSDBID=NBK1477:C0410529:146000:429:205468002,NBK1366:C1300257:187601:389158007|.|.;CLNDBN=Hypochondroplasia,Thanatophoric dysplasia\x2c type 2|Multiple myeloma\x2c somatic|Spermatocytic seminoma\x2c somatic;CLNACC=RCV000017757.1,RCV000017728.1|RCV000017729.1|RCV000017730.1 +4 1807890 rs121913105 A T . . RSPOS=1807890;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1807890A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0015;CLNSIG=5|5;CLNDSDB=NCBI|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=C2674173|NBK1366:C1868678:187600:85165;CLNDBN=Achondroplasia\x2c severe\x2c with developmental delay and acanthosis nigricans|Thanatophoric dysplasia type 1;CLNACC=RCV000017749.1|RCV000017750.1 +4 1807891 rs28928868 G C,T . . RSPOS=1807891;dbSNPBuildID=131;SSR=0;SAO=0;VP=050260000a01000402110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;HD;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000004.11:g.1807891G>C,NC_000004.11:g.1807891G>T;CLNSRC=.,.;CLNORIGIN=.,.;CLNSRCID=.,.;CLNSIG=5,1;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +4 1808331 rs121913480 G T . . RSPOS=1808331;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1808331G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1808371 rs104886023 G T . . RSPOS=1808371;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1808371G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1808377 rs104886024 G A . . RSPOS=1808377;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1808377G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1808948 rs121913481 CT CGA . . RSPOS=1808949;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060001201000002100220;GENEINFO=FGFR3:2261;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.1808949delinsGA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 1808987 rs121913101 T A,G . . RSPOS=1808987;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000201000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000004.11:g.1808987T>A,NC_000004.11:g.1808987T>G;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=.,134934.0007;CLNSIG=4,5;CLNDSDB=.,GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=.,NBK1366:C1868678:187600:85165;CLNDBN=.,Thanatophoric dysplasia type 1;CLNACC=.,RCV000017737.1 +4 1808989 rs121913103 A T . . RSPOS=1808989;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000201000002110100;GENEINFO=FGFR3:2261;WGT=1;VC=SNV;PM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.1808989A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=134934.0009;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1366:C1868678:187600:85165;CLNDBN=Thanatophoric dysplasia type 1;CLNACC=RCV000017739.1 +4 55141018 rs121908589 A G . . RSPOS=55141018;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=PDGFRA:5156;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55141018A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=173490.0010;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastrointestinal stromal tumor\x2c familial;CLNACC=RCV000014511.1 +4 55141036 rs121908586 T A . . RSPOS=55141036;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=PDGFRA:5156;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55141036T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=173490.0004;CLNSIG=255|5;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Gastrointestinal stromal tumor\x2c somatic|Gastrointestinal stromal tumor\x2c familial;CLNACC=RCV000014504.1|RCV000014505.1 +4 55141049 rs121913271 CAGCCCAGATGGACATGAA CCGC . . RSPOS=55141050;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000201000002100220;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55141050_55141067delinsCGC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55141050 rs121913270 AGCCCAGATGGACATG A . . RSPOS=55141051;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55141051_55141065delGCCCAGATGGACATG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55144547 rs121908587 C T . . RSPOS=55144547;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PDGFRA:5156;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55144547C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=173490.0008;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hypereosinophilic syndrome\x2c idiopathic\x2c resistant to imatinib;CLNACC=RCV000014509.1 +4 55152088 rs121913269 CAGAGAC C . . RSPOS=55152089;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152089_55152094delAGAGAC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152091 rs121913264 AGA AAT . . RSPOS=55152092;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100820;GENEINFO=PDGFRA:5156;WGT=1;VC=MNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152092_55152093delinsAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152091 rs121913262 AGACATCATG A . . RSPOS=55152092;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152092_55152100delGACATCATG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152091 rs121913261 AGACATCATGCAT A . . RSPOS=55152092;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152092_55152103delGACATCATGCAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152091 rs121913259 AGACATCATGCATG AA . . RSPOS=55152092;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152092_55152104delinsA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152092 rs121913260 GACATCATGCA GT . . RSPOS=55152093;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152093_55152102delinsT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152092 rs121913258 GACATCATGCATGAT GGA . . RSPOS=55152093;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152093_55152106delACATCATGCATGATinsGA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152093 rs121908585 A T . . RSPOS=55152093;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PDGFRA:5156;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152093A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=173490.0001;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastrointestinal stromal tumor\x2c somatic;CLNACC=RCV000014501.1 +4 55152093 rs121913257 ACATCATGCATGAT AG . . RSPOS=55152094;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152094_55152106delCATCATGCATGATinsG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152093 rs121913263 ACATCATGCATGATTCG AGGCC . . RSPOS=55152094;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152094_55152109delinsGGCC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152094 rs121913267 CATCATGCATGAT C . . RSPOS=55152095;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152095_55152106delATCATGCATGAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152095 rs121913268 ATCATGCATGATT A . . RSPOS=55152096;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=PDGFRA:5156;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152096_55152107delTCATGCATGATT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152101 rs121913266 CATGATTCGAA CC . . RSPOS=55152102;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100220;WGT=1;VC=DIV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152102_55152111delinsC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55152104 rs121908588 G T . . RSPOS=55152104;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=PDGFRA:5156;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55152104G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=173490.0009;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastrointestinal stromal tumor\x2c familial;CLNACC=RCV000014510.1 +4 55561764 rs121913505 G A . . RSPOS=55561764;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55561764G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593581 rs121913234 GAAACCCATGTATGAAGTACAGTGGAAG G . . RSPOS=55593582;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=KIT:3815;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593582_55593608del27;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593603 rs121913235 T A,C,G . . RSPOS=55593603;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100124;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000004.11:g.55593603T>A,NC_000004.11:g.55593603T>C,NC_000004.11:g.55593603T>G;CLNSRC=.,.,.;CLNORIGIN=2,2,2;CLNSRCID=.,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +4 55593605 rs121913511 GAAGGTTGTT G . . RSPOS=55593606;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=KIT:3815;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593606_55593614delAAGGTTGTT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593605 rs121913510 GAAGGTTGTTGAGGAG G . . RSPOS=55593606;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=KIT:3815;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593606_55593620delAAGGTTGTTGAGGAG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593608 rs121913685 GGTT G . . RSPOS=55593609;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002110200;GENEINFO=KIT:3815;WGT=1;VC=DIV;PM;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593609_55593611delGTT;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0017;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastrointestinal stromal tumor\x2c familial;CLNACC=RCV000014873.1 +4 55593609 rs121913520 G A . . RSPOS=55593609;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593609G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593610 rs121913517 T A,C,G . . RSPOS=55593610;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110124;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000004.11:g.55593610T>A,NC_000004.11:g.55593610T>C,NC_000004.11:g.55593610T>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,.;CLNORIGIN=2,2,2;CLNSRCID=164920.0014,164920.0023,.;CLNSIG=255,5,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=Gastrointestinal stromal tumor\x2c somatic,Gastrointestinal stromal tumor\x2c familial,.;CLNACC=RCV000014870.1,RCV000014879.1,. +4 55593613 rs121913521 T A,G . . RSPOS=55593613;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000004.11:g.55593613T>A,NC_000004.11:g.55593613T>G;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +4 55593661 rs121913513 T C . . RSPOS=55593661;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593661T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55593681 rs121913680 G A . . RSPOS=55593681;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593681G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0006;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0080024:172800:2884:6479008;CLNDBN=Partial albinism;CLNACC=RCV000014861.1 +4 55593685 rs28933371 T G . . RSPOS=55593685;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593685T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0022;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0080024:172800:2884:6479008;CLNDBN=Partial albinism;CLNACC=RCV000014878.1 +4 55593689 rs121913515 C T . . RSPOS=55593689;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000301000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55593689C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55594221 rs121913512 A G . . RSPOS=55594221;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55594221A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0024;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastrointestinal stromal tumor\x2c familial;CLNACC=RCV000014880.1 +4 55594258 rs121913523 T C . . RSPOS=55594258;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55594258T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55594287 rs121913679 G A . . RSPOS=55594287;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55594287G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0001;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0080024:172800:2884:6479008;CLNDBN=Partial albinism;CLNACC=RCV000014855.1 +4 55595519 rs121913516 C T . . RSPOS=55595519;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55595519C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55599320 rs121913506 G C,T . . RSPOS=55599320;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000004.11:g.55599320G>C,NC_000004.11:g.55599320G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,2;CLNSRCID=164920.0021,164920.0018;CLNSIG=255,5;CLNDSDB=NCBI:OMIM:OMIM:Orphanet:SNOMED CT,.;CLNDSDBID=C0153594:273300:605288:842:363449006,.;CLNDBN=Malignant tumor of testis,Leukemia\x2c acute myeloid;CLNACC=RCV000014877.1,RCV000014874.1 +4 55599321 rs121913507 A T . . RSPOS=55599321;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55599321A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0009;CLNSIG=5|5|5;CLNDSDB=NCBI|.|.;CLNDSDBID=C0023461|.|.;CLNDBN=Mast cell leukemia|Mastocytosis with associated hematologic disorder|Mastocytosis\x2c adult sporadic;CLNACC=RCV000014864.1|RCV000014865.1|RCV000014866.1 +4 55599333 rs121913682 A G . . RSPOS=55599333;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55599333A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0010;CLNSIG=5;CLNDSDB=NCBI;CLNDSDBID=C0221013;CLNDBN=Mast cell disease\x2c systemic;CLNACC=RCV000014867.1 +4 55599340 rs121913514 T A . . RSPOS=55599340;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55599340T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55599348 rs121913524 T C . . RSPOS=55599348;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.55599348T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +4 55602694 rs121913509 G A . . RSPOS=55602694;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55602694G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0020;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Mastocytosis\x2c sporadic\x2c childhood-onset;CLNACC=RCV000014876.1 +4 55602718 rs121913687 A C . . RSPOS=55602718;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KIT:3815;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55602718A>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164920.0019;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0080024:172800:2884:6479008;CLNDBN=Partial albinism;CLNACC=RCV000014875.1 +4 55955106 rs121917766 G A . . RSPOS=55955106;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=KDR:3791;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55955106G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191306.0001;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hemangioma\x2c capillary infantile\x2c somatic;CLNACC=RCV000013110.1 +4 55972946 rs34231037 A G . . RSPOS=55972946;GMAF=0.0137;dbSNPBuildID=126;SSR=0;SAO=1;VP=050260000a01140516110100;GENEINFO=KDR:3791;WGT=1;VC=SNV;PM;S3D;NSM;REF;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000004.11:g.55972946A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191306.0002;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hemangioma\x2c capillary infantile\x2c susceptibility to;CLNACC=RCV000013111.1 +4 153247289 rs149680468 G A . . RSPOS=153247289;dbSNPBuildID=134;SSR=0;SAO=3;VP=050268000a01000002100120;GENEINFO=FBXW7:55294;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000004.11:g.153247289G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112174626 rs146007372 C A . . RSPOS=112174626;dbSNPBuildID=134;SSR=0;SAO=3;VP=050068000a01000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112174626C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112174631 rs121913331 C T . . RSPOS=112174631;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112174631C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112174650 rs28933379 G A . . RSPOS=112174650;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112174650G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=611731.0010;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastric cancer\x2c somatic;CLNACC=RCV000000839.1 +5 112175057 rs77056664 C A . . RSPOS=112175057;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175057C>A;CLNSRC=.;CLNORIGIN=0;CLNSRCID=.;CLNSIG=255;CLNDSDB=OMIM;CLNDSDBID=114500;CLNDBN=Familial colorectal cancer;CLNACC=. +5 112175207 rs121913462 G T . . RSPOS=112175207;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175207G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112175211 rs1801155 T A . . RSPOS=112175211;dbSNPBuildID=89;SSR=0;SAO=1;VP=050168000a01040002110100;GENEINFO=APC:324;WGT=1;VC=SNV;PM;PMC;SLO;NSM;REF;VLD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175211T>A;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=NBK1345|611731.0029;CLNSIG=255|255|5;CLNDSDB=.|NCBI|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=.|CN068448|NBK1345:CN074282:175100:733:70921007;CLNDBN=Adenomatous polyposis coli\x2c susceptibility to|Breast cancer\x2c susceptibility to|Adenomatous polyposis coli;CLNACC=RCV000000864.1|RCV000000865.1|RCV000020088.1 +5 112175212 rs121913224 AAAAGA A . . RSPOS=112175218;dbSNPBuildID=133;SSR=0;SAO=3;VP=050168001201000002110220;GENEINFO=APC:324;WGT=1;VC=DIV;PM;PMC;SLO;NSF;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175218_112175222delAAAGA;CLNSRC=GeneReviews|OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=NBK1345|611731.0023|611731.0041;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|NCBI:SNOMED CT|.;CLNDSDBID=NBK1345:CN074282:175100:733:70921007|C0017097:60876000|.;CLNDBN=Adenomatous polyposis coli|Gardner syndrome|Adenomatous polyposis coli with congenital cholesteatoma;CLNACC=RCV000000856.1|RCV000000857.1|RCV000000858.1 +5 112175240 rs1801166 G C . . RSPOS=112175240;GMAF=0.0037;dbSNPBuildID=89;SSR=0;SAO=1;VP=050168000a01040516110100;GENEINFO=APC:324;WGT=1;VC=SNV;PM;PMC;SLO;NSM;REF;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175240G>C;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=NBK1345|611731.0036;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1345:CN074282:175100:733:70921007;CLNDBN=Adenomatous polyposis coli;CLNACC=RCV000000872.1 +5 112175303 rs121913327 C T . . RSPOS=112175303;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002110120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175303C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=611731.0009;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Colorectal cancer\x2c somatic;CLNACC=RCV000000838.1 +5 112175390 rs121913328 C T . . RSPOS=112175390;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175390C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112175423 rs121913329 C T . . RSPOS=112175423;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175423C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112175474 rs137854578 A T . . RSPOS=112175474;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175474A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=611731.0024;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hepatoblastoma\x2c somatic;CLNACC=RCV000000859.1 +5 112175576 rs74535574 C A,T . . RSPOS=112175576;dbSNPBuildID=131;SSR=0;SAO=3;VP=050060000e01000002110120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000005.9:g.112175576C>A,NC_000005.9:g.112175576C>T;CLNSRC=.,.;CLNORIGIN=0,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +5 112175639 rs121913332 C T . . RSPOS=112175639;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=APC:324;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175639C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112175676 rs121913334 AGA A . . RSPOS=112175683;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=APC:324;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175683_112175684delGA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 112175770 rs41115 G A . . RSPOS=112175770;RV;GMAF=0.3384;dbSNPBuildID=76;SSR=0;SAO=1;VP=05016800030115051f110101;GENEINFO=APC:324;WGT=1;VC=SNV;PM;PMC;SLO;REF;SYN;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM;GCF;CLNALLE=1;CLNHGVS=NC_000005.9:g.112175770G>A;CLNSRC=.;CLNORIGIN=0;CLNSRCID=.;CLNSIG=255;CLNDSDB=OMIM;CLNDSDBID=114500;CLNDBN=Familial colorectal cancer;CLNACC=. +5 149433644 rs121913392 A T . . RSPOS=149433644;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=CSF1R:1436;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.149433644A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 149433645 rs1801271 T A,C . . RSPOS=149433645;RV;dbSNPBuildID=89;SSR=0;SAO=3;VP=050160000a01000102110120;GENEINFO=CSF1R:1436;WGT=1;VC=SNV;PM;SLO;NSM;REF;GNO;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000005.9:g.149433645T>A,NC_000005.9:g.149433645T>C;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +5 149433646 rs121913393 A G . . RSPOS=149433646;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=CSF1R:1436;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000005.9:g.149433646A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +5 149453044 rs121913390 A G,T . . RSPOS=149453044;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000e01000002100120;GENEINFO=CSF1R:1436;WGT=1;VC=SNV;PM;NSM;NSN;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000005.9:g.149453044A>G,NC_000005.9:g.149453044A>T;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +7 55241707 rs28929495 G A,T . . RSPOS=55241707;dbSNPBuildID=132;SSR=0;SAO=3;VP=050068000a01000002110120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.55241707G>A,NC_000007.13:g.55241707G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=131550.0005,131550.0004;CLNSIG=6,6;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=Nonsmall cell lung cancer\x2c response to tyrosine kinase inhibitor in\x2c somatic,Nonsmall cell lung cancer\x2c response to tyrosine kinase inhibitor in\x2c somatic;CLNACC=RCV000018087.1,RCV000018086.1 +7 55242418 rs121913434 C T . . RSPOS=55242418;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242418C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242423 rs121913467 G A . . RSPOS=55242423;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242423G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242428 rs121913446 C T . . RSPOS=55242428;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242428C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242430 rs121913420 G A . . RSPOS=55242430;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242430G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242433 rs121913430 G A . . RSPOS=55242433;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242433G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242455 rs121913466 T C . . RSPOS=55242455;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242455T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242464 rs121913433 A G . . RSPOS=55242464;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242464A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242464 rs121913421 AGGAATTAAGAGAAGC A . . RSPOS=55242465;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242465_55242479delGGAATTAAGAGAAGC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242466 rs121913425 GAATTAAGAGAAGCAA G . . RSPOS=55242467;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242467_55242481delAATTAAGAGAAGCAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242466 rs121913422 GAATTAAGAGAAGCAACAT G . . RSPOS=55242467;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242467_55242484del18;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242466 rs121913424 GAATTAAGAGAAGCAACATCT GTC . . RSPOS=55242467;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100220;WGT=1;VC=DIV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242467_55242486delinsTC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242468 rs121913436 ATTAAGAGAA A . . RSPOS=55242469;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242469_55242477delTTAAGAGAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242468 rs121913440 ATTAAGAGAAGCAACATCT A . . RSPOS=55242469;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242469_55242486del18;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242468 rs121913437 ATTAAGAGAAGCAACATCTCC ACA . . RSPOS=55242469;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100220;WGT=1;VC=DIV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242469_55242488delinsCA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242469 rs121913441 TTAAGAGAAGCAA T . . RSPOS=55242470;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242470_55242481delTAAGAGAAGCAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242469 rs121913442 TTAAGAGAAGCAACAT T . . RSPOS=55242470;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242470_55242484delTAAGAGAAGCAACAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242469 rs121913438 TTAAGAGAAGCAACATCTC T . . RSPOS=55242470;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242470_55242487del18;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242470 rs121913439 TAAGA TCCCG . . RSPOS=55242471;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100820;GENEINFO=EGFR:1956;WGT=1;VC=MNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242471_55242474delinsCCCG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242478 rs121913229 G C . . RSPOS=55242478;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242478G>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242483 rs121913463 ATCTCCGAAAGCCAACAAGGAAATC A . . RSPOS=55242484;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=EGFR:1956;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242484_55242507del24;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242485 rs121913464 C A . . RSPOS=55242485;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242485C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55242487 rs121913231 C T . . RSPOS=55242487;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55242487C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55249005 rs121913465 G T . . RSPOS=55249005;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000001000002100120;GENEINFO=EGFR:1956|LOC100507500:100507500;WGT=1;VC=SNV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55249005G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55249071 rs121434569 C T . . RSPOS=55249071;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060000001000002110120;GENEINFO=EGFR:1956|LOC100507500:100507500;WGT=1;VC=SNV;PM;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.55249071C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=131550.0006;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Nonsmall cell lung cancer\x2c resistance to tyrosine kinase inhibitor in;CLNACC=RCV000018088.1 +7 55249130 rs121913230 G A . . RSPOS=55249130;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000001000002100120;GENEINFO=EGFR:1956|LOC100507500:100507500;WGT=1;VC=SNV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55249130G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55249131 rs121913431 G A . . RSPOS=55249131;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000001000002100120;GENEINFO=EGFR:1956|LOC100507500:100507500;WGT=1;VC=SNV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55249131G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55259486 rs104886012 G A,T . . RSPOS=55259486;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060000301000002110120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;REF;SYN;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.55259486G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55259524 rs121913444 T A . . RSPOS=55259524;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.55259524T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55259544 rs104886013 G A . . RSPOS=55259544;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.55259544G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 55259575 rs104886014 G A . . RSPOS=55259575;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060080001000002110120;GENEINFO=EGFR:1956;WGT=1;VC=SNV;PM;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.55259575G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 116411990 rs56391007 C T . . RSPOS=116411990;GMAF=0.0055;dbSNPBuildID=129;SSR=0;SAO=3;VP=050068000a01040016100120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;PMC;NSM;REF;VLD;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.116411990C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 116417463 rs121913244 C T . . RSPOS=116417463;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.116417463C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 116417464 rs121913243 A G . . RSPOS=116417464;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.116417464A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164860.0007;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0007134:605074:47044:41607009;CLNDBN=Renal cell carcinoma\x2c papillary\x2c 1;CLNACC=RCV000014901.1 +7 116423407 rs121913671 G A . . RSPOS=116423407;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423407G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164860.0004;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0007134:605074:47044:41607009;CLNDBN=Renal cell carcinoma\x2c papillary\x2c 1;CLNACC=RCV000014898.1 +7 116423413 rs121913247 T C . . RSPOS=116423413;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423413T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 116423414 rs121913246 A G . . RSPOS=116423414;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423414A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164860.0005;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0007134:605074:47044:41607009;CLNDBN=Renal cell carcinoma\x2c papillary\x2c 1;CLNACC=RCV000014899.1 +7 116423456 rs121913677 A G . . RSPOS=116423456;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423456A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164860.0010;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hepatocellular carcinoma\x2c childhood type\x2c somatic;CLNACC=RCV000014904.1 +7 116423474 rs121913245 T C . . RSPOS=116423474;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423474T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 116423475 rs121913676 G A . . RSPOS=116423475;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=MET:4233;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.116423475G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164860.0009;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hepatocellular carcinoma\x2c childhood type\x2c somatic;CLNACC=RCV000014903.1 +7 128850341 rs121918347 G T . . RSPOS=128850341;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=SMO:6608;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.128850341G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601500.0001;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Basal cell carcinoma\x2c sporadic;CLNACC=RCV000008586.1 +7 140453120 rs121913372 ACT AAA . . RSPOS=140453121;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100820;GENEINFO=BRAF:673;WGT=1;VC=MNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453121_140453122delinsAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453121 rs121913373 C T . . RSPOS=140453121;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453121C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453128 rs104886015 G A . . RSPOS=140453128;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453128G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453131 rs121913226 ATTT A . . RSPOS=140453132;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=BRAF:673;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453132_140453134delTTT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453132 rs121913365 T G . . RSPOS=140453132;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453132T>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453134 rs121913364 T C . . RSPOS=140453134;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453134T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164757.0005;CLNSIG=255|255;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Colorectal cancer\x2c somatic|Thyroid carcinoma\x2c follicular\x2c somatic;CLNACC=RCV000014999.1|RCV000015000.1 +7 140453134 rs121913377 TCA TAT . . RSPOS=140453135;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100820;GENEINFO=BRAF:673;WGT=1;VC=MNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453135_140453136delinsAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453135 rs121913227 CAC CCT,CTT . . RSPOS=140453136;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100820;GENEINFO=BRAF:673;WGT=1;VC=MNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140453136_140453137delACinsCT,NC_000007.13:g.140453136_140453137delACinsTT;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +7 140453136 rs113488022 A G,T . . RSPOS=140453136;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050268000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140453136A>G,NC_000007.13:g.140453136A>T;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=.,164757.0001;CLNSIG=255,255|255|255|255|255;CLNDSDB=.,.|.|.|.|.;CLNDSDBID=.,.|.|.|.|.;CLNDBN=.,Melanoma\x2c malignant\x2c somatic|Colorectal cancer\x2c somatic|Thyroid carcinoma\x2c papillary\x2c somatic|Astrocytoma\x2c low-grade\x2c somatic|NONSEMINOMATOUS GERM CELL TUMORS\x2c SOMATIC;CLNACC=.,RCV000014991.1|RCV000014992.1|RCV000014993.1|RCV000014994.1|RCV000022677.1 +7 140453137 rs121913378 C A,T . . RSPOS=140453137;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140453137C>A,NC_000007.13:g.140453137C>T;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +7 140453137 rs121913374 CT CCGTAGTA . . RSPOS=140453138;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000301000002100220;WGT=1;VC=DIV;PM;S3D;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453138delinsCGTAGTA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453139 rs121913375 G A . . RSPOS=140453139;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453139G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453144 rs121913368 TAG TGA . . RSPOS=140453145;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100820;GENEINFO=BRAF:673;WGT=1;VC=MNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453145_140453146delAGinsGA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453146 rs121913369 G C . . RSPOS=140453146;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453146G>C;CLNSRC=OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164757.0008|164757.0026;CLNSIG=255|5;CLNDSDB=.|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=.|NBK1124:C3150970:613706:648;CLNDBN=Nonsmall cell lung cancer\x2c somatic|Noonan syndrome 7;CLNACC=RCV000015003.1|RCV000030948.1 +7 140453149 rs121913361 C G . . RSPOS=140453149;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453149C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453150 rs121913341 A C . . RSPOS=140453150;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453150A>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453151 rs121913225 A G . . RSPOS=140453151;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453151A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453153 rs121913337 A T . . RSPOS=140453153;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453153A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453154 rs121913338 T A,C . . RSPOS=140453154;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140453154T>A,NC_000007.13:g.140453154T>C;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=.,164757.0011;CLNSIG=255,255;CLNDSDB=.,SNOMED CT;CLNDSDBID=.,118601006;CLNDBN=.,Non-Hodgkin's lymphoma;CLNACC=.,RCV000015006.1 +7 140453159 rs121913362 T C . . RSPOS=140453159;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453159T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453161 rs121913363 T C . . RSPOS=140453161;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453161T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453174 rs121913336 G T . . RSPOS=140453174;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453174G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453175 rs121913335 T G . . RSPOS=140453175;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453175T>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453179 rs121913340 C T . . RSPOS=140453179;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453179C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140453193 rs121913370 T C . . RSPOS=140453193;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140453193T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140481397 rs121913376 C A . . RSPOS=140481397;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481397C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140481400 rs121913358 TTCC TACT,TGCT . . RSPOS=140481401;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000201000002100820;GENEINFO=BRAF:673;WGT=1;VC=MNV;PM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140481401_140481403delinsACT,NC_000007.13:g.140481401_140481403delinsGCT;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +7 140481402 rs121913355 C A,G,T . . RSPOS=140481402;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000007.13:g.140481402C>A,NC_000007.13:g.140481402C>G,NC_000007.13:g.140481402C>T;CLNSRC=.,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,1,2;CLNSRCID=.,164757.0010,164757.0014;CLNSIG=255,255,5;CLNDSDB=.,SNOMED CT,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=.,118601006,NBK1186:C1275081:115150:1340:403770008;CLNDBN=.,Non-Hodgkin's lymphoma,Cardio-facio-cutaneous syndrome;CLNACC=.,RCV000015005.1,RCV000015008.1 +7 140481403 rs121913357 C G,T . . RSPOS=140481403;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140481403C>G,NC_000007.13:g.140481403C>T;CLNSRC=OMIM Allelic Variant,.;CLNORIGIN=1,2;CLNSRCID=164757.0009,.;CLNSIG=255,255;CLNDSDB=SNOMED CT,.;CLNDSDBID=118601006,.;CLNDBN=Non-Hodgkin's lymphoma,.;CLNACC=RCV000015004.1,. +7 140481411 rs121913351 C A,G,T . . RSPOS=140481411;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000007.13:g.140481411C>A,NC_000007.13:g.140481411C>G,NC_000007.13:g.140481411C>T;CLNSRC=OMIM Allelic Variant,.,.;CLNORIGIN=2,2,2;CLNSRCID=164757.0006,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=Adenocarcinoma of lung\x2c somatic,.,.;CLNACC=RCV000015001.1,.,. +7 140481412 rs121913353 C G . . RSPOS=140481412;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481412C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140481417 rs121913348 C A,T . . RSPOS=140481417;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000007.13:g.140481417C>A,NC_000007.13:g.140481417C>T;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,2;CLNSRCID=.,164757.0004;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,Colorectal cancer\x2c somatic;CLNACC=.,RCV000014997.1 +7 140481418 rs121913349 C G . . RSPOS=140481418;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481418C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +7 140481420 rs180177033 A C . . RSPOS=140481420;RV;dbSNPBuildID=135;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481420A>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164757.0003;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Colorectal cancer\x2c somatic;CLNACC=RCV000014996.1 +7 140481423 rs180177032 C A . . RSPOS=140481423;RV;dbSNPBuildID=135;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481423C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164757.0002;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Colon cancer\x2c somatic;CLNACC=RCV000014995.1 +7 140481478 rs121913371 G A . . RSPOS=140481478;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=BRAF:673;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000007.13:g.140481478G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +8 38282208 rs121909627 G C . . RSPOS=38282208;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=FGFR1:2260;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000008.10:g.38282208G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=136350.0001;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1455:C1863356:101600:C1863356:710|NBK1455:C0795998:123150:1540;CLNDBN=Pfeiffer syndrome|Jackson-Weiss syndrome;CLNACC=RCV000017669.1|RCV000017670.1 +8 38282214 rs121909645 C T . . RSPOS=38282214;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=FGFR1:2260;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000008.10:g.38282214C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=136350.0025;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1334:C1563720:147950:478;CLNDBN=Kallmann syndrome 2;CLNACC=RCV000030940.1 +9 5073742 rs121912472 G C . . RSPOS=5073742;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=JAK2:3717;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.5073742G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=147796.0002;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Leukemia\x2c acute myelogenous\x2c somatic;CLNACC=RCV000015773.1 +9 5073770 rs77375493 G T . . RSPOS=5073770;GMAF=0;dbSNPBuildID=131;SSR=0;SAO=3;VP=050260000a01000416110120;GENEINFO=JAK2:3717;WGT=1;VC=SNV;PM;S3D;NSM;REF;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.5073770G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=147796.0001;CLNSIG=255|255|255|255|255|255;CLNDSDB=.|.|.|.|.|.;CLNDSDBID=.|.|.|.|.|.;CLNDBN=Polycythemia vera\x2c somatic|Myelofibrosis\x2c somatic|Leukemia\x2c acute myelogenous\x2c somatic|Budd-Chiari syndrome\x2c susceptibility to\x2c somatic|THROMBOCYTHEMIA 3\x2c SOMATIC|ERYTHROCYTOSIS\x2c SOMATIC;CLNACC=RCV000015769.1|RCV000015770.1|RCV000015771.1|RCV000015772.1|RCV000022627.1|RCV000022628.1 +9 21971153 rs121913383 C A . . RSPOS=21971153;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260800e01000002100120;GENEINFO=CDKN2A:1029;WGT=1;VC=SNV;PM;S3D;NSM;NSN;REF;U3;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.21971153C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 21971177 rs121913382 C A . . RSPOS=21971177;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260800e01000002100120;GENEINFO=CDKN2A:1029;WGT=1;VC=SNV;PM;S3D;NSM;NSN;REF;U3;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.21971177C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 21971186 rs121913387 G A . . RSPOS=21971186;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260800e01000002100120;GENEINFO=CDKN2A:1029;WGT=1;VC=SNV;PM;S3D;NSM;NSN;REF;U3;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.21971186G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 21971188 rs140844717 G GC . . RSPOS=21971189;dbSNPBuildID=134;SSR=0;SAO=3;VP=050068801201000002100220;GENEINFO=CDKN2A:1029;WGT=1;VC=DIV;PM;PMC;NSF;REF;U3;OTHERKG;LSD;CLNALLE=-1;CLNHGVS=NC_000009.11:g.21971189dupC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 80409488 rs121913492 T A,G . . RSPOS=80409488;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=GNAQ:2776;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000009.11:g.80409488T>A,NC_000009.11:g.80409488T>G;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +9 133738330 rs121913456 A G . . RSPOS=133738330;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738330A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133738342 rs121913455 C G . . RSPOS=133738342;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738342C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133738349 rs121913453 G A . . RSPOS=133738349;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738349G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133738356 rs121913458 G C . . RSPOS=133738356;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738356G>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133738357 rs121913461 T C . . RSPOS=133738357;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738357T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=189980.0004;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Leukemia\x2c philadelphia chromosome-positive\x2c resistant to imatinib;CLNACC=RCV000013462.1 +9 133738358 rs121913460 A T . . RSPOS=133738358;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738358A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133738363 rs121913448 G A . . RSPOS=133738363;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738363G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=189980.0003;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Leukemia\x2c philadelphia chromosome-positive\x2c resistant to imatinib;CLNACC=RCV000013461.1 +9 133738364 rs121913449 A T . . RSPOS=133738364;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133738364A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=189980.0002;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Leukemia\x2c philadelphia chromosome-positive\x2c resistant to imatinib;CLNACC=RCV000013460.1 +9 133747520 rs121913447 A G . . RSPOS=133747520;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133747520A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133748270 rs137853304 T C . . RSPOS=133748270;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748270T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=189980.0005;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Chronic myeloid leukemia\x2c resistant to imatinib;CLNACC=RCV000013463.1 +9 133748283 rs121913459 C T . . RSPOS=133748283;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748283C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=189980.0001;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Leukemia\x2c philadelphia chromosome-positive\x2c resistant to imatinib;CLNACC=RCV000013459.1 +9 133748290 rs121913451 C G . . RSPOS=133748290;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748290C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133748391 rs121913457 T C . . RSPOS=133748391;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748391T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=189980.0006;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Chronic myeloid leukemia\x2c resistant to imatinib;CLNACC=RCV000013464.1 +9 133748403 rs121913450 A G . . RSPOS=133748403;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748403A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133748414 rs121913452 T G . . RSPOS=133748414;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133748414T>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +9 133750356 rs121913454 A G . . RSPOS=133750356;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=ABL1:25;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000009.11:g.133750356A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609069 rs77558292 T C . . RSPOS=43609069;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609069T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0042;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C1833921:155240:1332|.;CLNDBN=Familial medullary thyroid carcinoma|MEN2A and FMTC;CLNACC=RCV000014971.1|RCV000021776.1 +10 43609070 rs77939446 G A . . RSPOS=43609070;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609070G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0029;CLNSIG=5|5;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=MULTIPLE ENDOCRINE NEOPLASIA\x2c TYPE IIA\x2c WITH HIRSCHSPRUNG DISEASE|MEN2A and FMTC;CLNACC=RCV000014958.1|RCV000021778.1 +10 43609077 rs80069458 C G . . RSPOS=43609077;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609077C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0007;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|MEN2A and FMTC;CLNACC=RCV000014932.1|RCV000021788.1 +10 43609077 rs121913313 CTTCCCTGAGGAGGAGAAGTGCTTCTGC C . . RSPOS=43609078;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609078_43609104del27;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609096 rs76262710 T C,G . . RSPOS=43609096;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.43609096T>C,NC_000010.10:g.43609096T>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=164761.0025,164761.0001;CLNSIG=5|5,5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.,GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C1833921:155240:1332|.,NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Familial medullary thyroid carcinoma|MEN2A and FMTC,Multiple endocrine neoplasia\x2c type 2a|MEN2A and Unclassified;CLNACC=RCV000014954.1|RCV000021792.1,RCV000014919.1|RCV000021793.1 +10 43609097 rs79781594 G C . . RSPOS=43609097;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609097G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0008;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1257:C1833921:155240:1332|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Familial medullary thyroid carcinoma|MEN2A and FMTC;CLNACC=RCV000014933.1|RCV000014934.1|RCV000021791.1 +10 43609102 rs77316810 T C . . RSPOS=43609102;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609102T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0009;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|MEN2A and FMTC;CLNACC=RCV000014935.1|RCV000021799.1 +10 43609103 rs77503355 G A,C,T . . RSPOS=43609103;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01000002110104;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000010.10:g.43609103G>A,NC_000010.10:g.43609103G>C,NC_000010.10:g.43609103G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=0,1,1;CLNSRCID=164761.0010,164761.0041,164761.0024;CLNSIG=5|5,5|5|5,5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.,GeneReviews:NCBI:OMIM:Orphanet|.|.,GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|.,NBK1257:C1833921:155240:1332|.|.,NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|MEN2A and FMTC,Familial medullary thyroid carcinoma|MEN2A and Unclassified|MEN2A and FMTC,Multiple endocrine neoplasia\x2c type 2a|MEN2A and FMTC;CLNACC=RCV000014936.1|RCV000021801.1,RCV000014970.1|RCV000021798.1|RCV000021802.1,RCV000014953.1|RCV000021803.1 +10 43609104 rs79890926 C G . . RSPOS=43609104;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609104C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0032;CLNSIG=5|5;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=MULTIPLE ENDOCRINE NEOPLASIA\x2c TYPE IIA\x2c WITH HIRSCHSPRUNG DISEASE|MEN2A and Unclassified;CLNACC=RCV000014959.1|RCV000021789.1 +10 43609926 rs193922699 A G . . RSPOS=43609926;dbSNPBuildID=136;SSR=0;SAO=1;VP=050068200001000002100100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;ASS;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609926A>G;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609940 rs121913308 A G . . RSPOS=43609940;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609940A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=MEN2 phenotype: Unknown;CLNACC=RCV000021814.1 +10 43609940 rs121913307 ACGAGCT A . . RSPOS=43609941;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609941_43609946delCGAGCT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609941 rs121913312 CGAGCTG C . . RSPOS=43609942;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609942_43609947delGAGCTG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609942 rs121913311 GAGC G . . RSPOS=43609943;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000201000002100200;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609943_43609945delAGC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609942 rs121913310 GAGCTGTGCCGCACGGTGATCGCAG GTGCGGC . . RSPOS=43609943;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000201000002100220;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609943_43609966delinsTGCGGC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43609944 rs267607009 G C,T . . RSPOS=43609944;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=-1;CLNHGVS=NC_000010.10:g.43609944G>Y;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=164761.0002;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009;CLNDBN=Multiple endocrine neoplasia\x2c type 2a;CLNACC=RCV000014920.1 +10 43609945 rs267607010 C G . . RSPOS=43609945;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609945C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=164761.0002;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009;CLNDBN=Multiple endocrine neoplasia\x2c type 2a;CLNACC=RCV000014920.1 +10 43609948 rs75076352 T C,G . . RSPOS=43609948;dbSNPBuildID=131;SSR=0;SAO=3;VP=050068000a01000002110120;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.43609948T>C,NC_000010.10:g.43609948T>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=164761.0011,164761.0003;CLNSIG=5|5|5,5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.,GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1548:C0031511:171300:29072|.,NBK1257:C0025268:171400:247698:653:61808009|NBK1548:C0031511:171300:29072|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Pheochromocytoma|MEN2A and FMTC,Multiple endocrine neoplasia\x2c type 2a|Pheochromocytoma|MEN2A and Unclassified;CLNACC=RCV000014937.1|RCV000014938.1|RCV000021821.1,RCV000014922.1|RCV000014923.1|RCV000021822.1 +10 43609949 rs75996173 G A,C,T . . RSPOS=43609949;dbSNPBuildID=131;SSR=0;SAO=3;VP=050068000a01000002110124;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000010.10:g.43609949G>A,NC_000010.10:g.43609949G>C,NC_000010.10:g.43609949G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=2,1,0;CLNSRCID=164761.0004,164761.0005,164761.0006;CLNSIG=5|5|5,5|5|5|5,5|5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.,GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.|.,GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1548:C0031511:171300:29072|.,NBK1257:C0025268:171400:247698:653:61808009|NBK1548:C0031511:171300:29072|.|.,NBK1257:C0025268:171400:247698:653:61808009|NBK1257:C1833921:155240:1332|NBK1548:C0031511:171300:29072|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Pheochromocytoma|MEN2A and FMTC,Multiple endocrine neoplasia\x2c type 2a|Pheochromocytoma|MEN2A and Unclassified|MEN2A and FMTC,Multiple endocrine neoplasia\x2c type 2a|Familial medullary thyroid carcinoma|Pheochromocytoma|MEN2A and FMTC;CLNACC=RCV000014924.1|RCV000014925.1|RCV000021823.1,RCV000014926.1|RCV000014927.1|RCV000021820.1|RCV000021824.1,RCV000014928.1|RCV000014929.1|RCV000014930.1|RCV000021825.1 +10 43609950 rs77709286 C G . . RSPOS=43609950;dbSNPBuildID=131;SSR=0;SAO=3;VP=050068000a01000002110120;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609950C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164761.0012;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1548:C0031511:171300:29072|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Pheochromocytoma|MEN2A and FMTC;CLNACC=RCV000014939.1|RCV000014940.1|RCV000021827.1 +10 43609967 rs78935588 C G . . RSPOS=43609967;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609967C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0040;CLNSIG=5|0;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|MEN2 phenotype: Unknown;CLNACC=RCV000014969.1|RCV000021832.1 +10 43609989 rs75225191 C T . . RSPOS=43609989;dbSNPBuildID=131;SSR=0;SAO=1;VP=050068000301000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;REF;SYN;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609989C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0037;CLNSIG=255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT:SNOMED CT;CLNDSDBID=NBK1439:CN030431:142623:388:204739008:A2933129;CLNDBN=Hirschsprung disease 1;CLNACC=RCV000014966.1 +10 43609990 rs77711105 G A . . RSPOS=43609990;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060000a01040002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;VLD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43609990G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0047;CLNSIG=5|0;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|MEN2 phenotype: Unknown;CLNACC=RCV000014976.1|RCV000021834.1 +10 43613829 rs75075748 T C . . RSPOS=43613829;dbSNPBuildID=131;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43613829T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0015;CLNSIG=255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT:SNOMED CT;CLNDSDBID=NBK1439:CN030431:142623:388:204739008:A2933129;CLNDBN=Hirschsprung disease 1;CLNACC=RCV000014921.1 +10 43613840 rs78014899 G A,C . . RSPOS=43613840;dbSNPBuildID=131;SSR=0;SAO=3;VP=050268000b01000002110120;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;SYN;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.43613840G>A,NC_000010.10:g.43613840G>C;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=0,2;CLNSRCID=.,164761.0027;CLNSIG=5,5|5|5;CLNDSDB=.,GeneReviews:NCBI:OMIM:Orphanet|.|.;CLNDSDBID=.,NBK1257:C1833921:155240:1332|.|.;CLNDBN=.,Familial medullary thyroid carcinoma|MEN2A and FMTC|MEN2 phenotype: Unclassified;CLNACC=.,RCV000014956.1|RCV000021842.1|RCV000021843.1 +10 43613868 rs75686697 G A . . RSPOS=43613868;dbSNPBuildID=131;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43613868G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0053;CLNSIG=5|0;CLNDSDB=NCBI:OMIM:Orphanet|.;CLNDSDBID=C1619700:191830:1848|.;CLNDBN=Renal adysplasia|MEN2 phenotype: Unknown;CLNACC=RCV000014983.1|RCV000021847.1 +10 43613906 rs75030001 G C . . RSPOS=43613906;dbSNPBuildID=131;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43613906G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0033;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1257:C1833921:155240:1332|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Familial medullary thyroid carcinoma|MEN2A and FMTC;CLNACC=RCV000014960.1|RCV000014961.1|RCV000021849.1 +10 43613908 rs77724903 A T . . RSPOS=43613908;dbSNPBuildID=131;SSR=0;SAO=1;VP=050268000a01040002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;VLD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43613908A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0034;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C1833921:155240:1332|NBK1548:C0031511:171300:29072|.;CLNDBN=Familial medullary thyroid carcinoma|Pheochromocytoma|MEN2A and FMTC;CLNACC=RCV000014962.1|RCV000014963.1|RCV000021851.1 +10 43615566 rs121913306 TAGC TTTT . . RSPOS=43615567;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000201000002100820;GENEINFO=RET:5979;WGT=1;VC=MNV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43615567_43615569delinsTTT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43615592 rs75234356 T G . . RSPOS=43615592;dbSNPBuildID=131;SSR=0;SAO=1;VP=050268000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43615592T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0049;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C0025268:171400:247698:653:61808009|NBK1257:C1833921:155240:1332|.;CLNDBN=Multiple endocrine neoplasia\x2c type 2a|Familial medullary thyroid carcinoma|MEN2A and FMTC;CLNACC=RCV000014978.1|RCV000014979.1|RCV000021875.1 +10 43615611 rs76087194 G A . . RSPOS=43615611;dbSNPBuildID=131;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43615611G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0016;CLNSIG=255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT:SNOMED CT;CLNDSDBID=NBK1439:CN030431:142623:388:204739008:A2933129;CLNDBN=Hirschsprung disease 1;CLNACC=RCV000014946.1 +10 43615612 rs121913309 AGATGTTTATGAA A . . RSPOS=43615613;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=RET:5979;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.43615613_43615624delGATGTTTATGAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 43615632 rs267607011 C G . . RSPOS=43615632;dbSNPBuildID=136;SSR=0;SAO=0;VP=050060000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43615632C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=.;CLNSRCID=164761.0043;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:Orphanet:SNOMED CT:SNOMED CT;CLNDSDBID=NBK1257:C0025269:162300:C1834211:247709:653:6153000:61530001;CLNDBN=Multiple endocrine neoplasia\x2c type 2b;CLNACC=RCV000014972.1 +10 43617398 rs78347871 G C,T . . RSPOS=43617398;dbSNPBuildID=131;SSR=0;SAO=1;VP=050268000a01000002110100;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43617398G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164761.0051;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1257:C1833921:155240:1332|.;CLNDBN=Familial medullary thyroid carcinoma|MEN2 phenotype: Unclassified;CLNACC=RCV000014981.1|RCV000021883.1 +10 43617416 rs74799832 T C . . RSPOS=43617416;dbSNPBuildID=131;SSR=0;SAO=3;VP=050268000a01000002110120;GENEINFO=RET:5979;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.43617416T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=164761.0013;CLNSIG=5|5|255|1;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:Orphanet:SNOMED CT:SNOMED CT|.|.|NCBI:OMIM:Orphanet;CLNDSDBID=NBK1257:C0025269:162300:C1834211:247709:653:6153000:61530001|.|.|C1619700:191830:1848;CLNDBN=Multiple endocrine neoplasia\x2c type 2b|Thyroid carcinoma\x2c sporadic medullary|Pheochromocytoma\x2c somatic|Renal adysplasia;CLNACC=RCV000014941.1|RCV000014942.1|RCV000014943.1|RCV000014944.1 +10 89624241 rs121913290 CAA C . . RSPOS=89624243;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=PTEN:5728|KLLN:100144748;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89624243_89624244delAA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89624281 rs121909233 G A . . RSPOS=89624281;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260020a01000002110100;GENEINFO=PTEN:5728|KLLN:100144748;WGT=1;VC=SNV;PM;S3D;NSM;REF;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89624281G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0025;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Malignant melanoma\x2c somatic;CLNACC=RCV000008285.1 +10 89685286 rs121909236 C G . . RSPOS=89685286;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89685286C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0030;CLNSIG=5;CLNDSDB=NCBI;CLNDSDBID=C2749240;CLNDBN=Vater association with macrocephaly and ventriculomegaly;CLNACC=RCV000008290.1 +10 89685314 rs121909226 T C . . RSPOS=89685314;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89685314T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0012;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C2676500:612359:201;CLNDBN=Cowden-like syndrome;CLNACC=RCV000008272.1 +10 89711892 rs121909221 T A . . RSPOS=89711892;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89711892T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0004;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1488:C0265326:153480:109;CLNDBN=Bannayan-Riley-Ruvalcaba syndrome;CLNACC=RCV000008259.1 +10 89711899 rs121913293 C T . . RSPOS=89711899;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89711899C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89711900 rs121913294 G A . . RSPOS=89711900;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89711900G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89711916 rs104894184 T A,G . . RSPOS=89711916;dbSNPBuildID=132;SSR=0;SAO=0;VP=050260000601000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.89711916T>A,NC_000010.10:g.89711916T>G;CLNSRC=.,.;CLNORIGIN=.,.;CLNSRCID=.,.;CLNSIG=1,1;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +10 89712015 rs121909232 C A . . RSPOS=89712015;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89712015C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0024;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Malignant melanoma\x2c somatic;CLNACC=RCV000008284.1 +10 89717615 rs121909227 C T . . RSPOS=89717615;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717615C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0015;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1488:C0265326:153480:109;CLNDBN=Bannayan-Riley-Ruvalcaba syndrome;CLNACC=RCV000008273.1 +10 89717624 rs121909234 G A . . RSPOS=89717624;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717624G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0026;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Malignant melanoma\x2c somatic;CLNACC=RCV000008286.1 +10 89717672 rs121909219 C T . . RSPOS=89717672;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717672C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0002;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1488:C0018553:158350:201:65285:58037000|NBK1488:C0265326:153480:109;CLNDBN=Cowden disease|Bannayan-Riley-Ruvalcaba syndrome;CLNACC=RCV000008256.1|RCV000008257.1 +10 89717676 rs121909235 G A . . RSPOS=89717676;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717676G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0029;CLNSIG=255|5;CLNDSDB=NCBI:OMIM:Orphanet|NCBI;CLNDSDBID=C2751642:613028:46484|C0025286;CLNDBN=Glioma susceptibility 2|Meningioma;CLNACC=RCV000008288.1|RCV000008289.1 +10 89717697 rs121909240 T C . . RSPOS=89717697;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717697T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0039;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C1854416:605309:210548;CLNDBN=Macrocephaly/autism syndrome;CLNACC=RCV000008300.1 +10 89717730 rs121909239 A G . . RSPOS=89717730;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717730A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0038;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C1854416:605309:210548;CLNDBN=Macrocephaly/autism syndrome;CLNACC=RCV000008299.1 +10 89717741 rs121909228 G T . . RSPOS=89717741;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717741G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0016;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1488:C0265326:153480:109;CLNDBN=Bannayan-Riley-Ruvalcaba syndrome;CLNACC=RCV000008274.1 +10 89717769 rs121913289 TA T . . RSPOS=89717775;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=PTEN:5728;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89717775delA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89720799 rs146650273 TACTT T . . RSPOS=89720804;dbSNPBuildID=134;SSR=0;SAO=3;VP=050268000601000002100220;GENEINFO=PTEN:5728;WGT=1;VC=DIV;PM;PMC;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89720804_89720807delACTT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89720811 rs121913291 CA C . . RSPOS=89720817;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=PTEN:5728;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.89720817delA;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 89720852 rs121909231 C T . . RSPOS=89720852;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=PTEN:5728;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.89720852C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=601728.0021;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet:Orphanet:SNOMED CT|NCBI;CLNDSDBID=NBK1488:C0265326:153480:109|NBK1488:C0018553:158350:201:65285:58037000|C1866398;CLNDBN=Bannayan-Riley-Ruvalcaba syndrome|Cowden disease|Proteus-like syndrome;CLNACC=RCV000008279.1|RCV000008280.1|RCV000008281.1 +10 123258034 rs121913476 A T . . RSPOS=123258034;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.123258034A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 123258105 rs121918507 T C . . RSPOS=123258105;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123258105T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0034;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|NCBI:OMIM:Orphanet;CLNDSDBID=NBK1455:C0010273:123500:207:28861008|C1865070:609579:168624;CLNDBN=Crouzon syndrome|Scaphocephaly\x2c maxillary retrusion\x2c and mental retardation;CLNACC=RCV000014220.1|RCV000014221.1 +10 123274774 rs121913474 A G . . RSPOS=123274774;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002100120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.123274774A>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 123274794 rs121913478 T C . . RSPOS=123274794;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002110120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123274794T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=176943.0015;CLNSIG=5|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1455:C1852406:123790:1555|.;CLNDBN=Cutis Gyrata syndrome of Beare and Stevenson|Endometrial cancer\x2c somatic;CLNACC=RCV000014198.1|RCV000014199.1 +10 123274803 rs121913477 G C . . RSPOS=123274803;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002110120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123274803G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0016;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1455:C1852406:123790:1555;CLNDBN=Cutis Gyrata syndrome of Beare and Stevenson;CLNACC=RCV000014200.1 +10 123279503 rs121913475 T C . . RSPOS=123279503;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060080a01000002100120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279503T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +10 123279558 rs121918500 T C . . RSPOS=123279558;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279558T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0020;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1455:C0010273:123500:207:28861008;CLNDBN=Crouzon syndrome;CLNACC=RCV000014204.1 +10 123279562 rs121918499 C A,G . . RSPOS=123279562;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.123279562C>A,NC_000010.10:g.123279562C>G;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=.,1;CLNSRCID=.,176943.0019;CLNSIG=5,5;CLNDSDB=.,GeneReviews:NCBI:OMIM:OMIM:Orphanet;CLNDSDBID=.,NBK1455:C1863356:101600:C1863356:710;CLNDBN=.,Pfeiffer syndrome;CLNACC=.,RCV000014203.1 +10 123279564 rs121918501 A C,G . . RSPOS=123279564;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000010.10:g.123279564A>C,NC_000010.10:g.123279564A>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=176943.0022,176943.0021;CLNSIG=5,5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1455:C0010273:123500:207:28861008,NBK1455:C0010273:123500:207:28861008;CLNDBN=Crouzon syndrome,Crouzon syndrome;CLNACC=RCV000014206.1,RCV000014205.1 +10 123279566 rs121918497 T G . . RSPOS=123279566;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279566T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0014;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1455:C0010273:123500:207:28861008|NBK1455:C0795998:123150:1540;CLNDBN=Crouzon syndrome|Jackson-Weiss syndrome;CLNACC=RCV000014196.1|RCV000014197.1 +10 123279612 rs121918503 CGTC C . . RSPOS=123279613;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060080001000002110200;GENEINFO=FGFR2:2263;WGT=1;VC=DIV;PM;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279613_123279615delGTC;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0027;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet;CLNDSDBID=NBK1455:C1863356:101600:C1863356:710;CLNDBN=Pfeiffer syndrome;CLNACC=RCV000014211.1 +10 123279633 rs121918505 A G . . RSPOS=123279633;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279633A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0029;CLNSIG=5|255;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet|.;CLNDSDBID=NBK1455:C1863356:101600:C1863356:710|.;CLNDBN=Pfeiffer syndrome|Gastric cancer\x2c somatic;CLNACC=RCV000014213.1|RCV000014214.1 +10 123279674 rs77543610 G C . . RSPOS=123279674;dbSNPBuildID=131;SSR=0;SAO=1;VP=050060080a01000402110100;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;HD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279674G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0011;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1455:C0001193:101200:87:205258009;CLNDBN=Apert syndrome;CLNACC=RCV000014193.1 +10 123279675 rs121918498 GCG GAA . . RSPOS=123279676;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060080a01000002110800;GENEINFO=FGFR2:2263;WGT=1;VC=MNV;PM;NSM;REF;INT;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279676_123279677delCGinsAA;CLNSRC=OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176943.0017|176943.0026;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1455:C0001193:101200:87:205258009;CLNDBN=Apert syndrome;CLNACC=RCV000014201.1 +10 123279677 rs79184941 G C . . RSPOS=123279677;RV;dbSNPBuildID=131;SSR=0;SAO=3;VP=050060080a01000402110120;GENEINFO=FGFR2:2263;WGT=1;VC=SNV;PM;NSM;REF;INT;HD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000010.10:g.123279677G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=176943.0010;CLNSIG=5|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1455:C0001193:101200:87:205258009|.;CLNDBN=Apert syndrome|Endometrial cancer\x2c somatic;CLNACC=RCV000014191.1|RCV000014192.1 +11 533869 rs121917756 C T . . RSPOS=533869;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.533869C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190020.0009;CLNSIG=5;CLNDSDB=NCBI;CLNDSDBID=C1968782;CLNDBN=Myopathy\x2c congenital\x2c with excess of muscle spindles;CLNACC=RCV000013442.1 +11 533873 rs121913496 C G . . RSPOS=533873;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000011.9:g.533873C>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +11 533874 rs121913233 T A,C,G . . RSPOS=533874;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100124;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000011.9:g.533874T>A,NC_000011.9:g.533874T>C,NC_000011.9:g.533874T>G;CLNSRC=.,.,.;CLNORIGIN=2,2,2;CLNSRCID=.,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +11 533875 rs28933406 G T . . RSPOS=533875;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.533875G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190020.0002;CLNSIG=255|255;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Thyroid carcinoma\x2c follicular\x2c somatic|Spermatocytic seminoma\x2c somatic;CLNACC=RCV000013434.1|RCV000022795.1 +11 533883 rs121917758 G A . . RSPOS=533883;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.533883G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190020.0011;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1507:C0587248:218040:3071:309776008;CLNDBN=Costello syndrome;CLNACC=RCV000013444.1 +11 534259 rs121917757 G T . . RSPOS=534259;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.534259G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190020.0010;CLNSIG=5;CLNDSDB=NCBI;CLNDSDBID=C1968782;CLNDBN=Myopathy\x2c congenital\x2c with excess of muscle spindles;CLNACC=RCV000013443.1 +11 534285 rs104894226 C A,T . . RSPOS=534285;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000011.9:g.534285C>A,NC_000011.9:g.534285C>T;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=.,190020.0005;CLNSIG=255,5;CLNDSDB=.,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=.,NBK1507:C0587248:218040:3071:309776008;CLNDBN=.,Costello syndrome;CLNACC=.,RCV000013438.1 +11 534286 rs104894228 C A,G,T . . RSPOS=534286;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000011.9:g.534286C>A,NC_000011.9:g.534286C>G,NC_000011.9:g.534286C>T;CLNSRC=OMIM Allelic Variant,.,.;CLNORIGIN=2,2,2;CLNSRCID=190020.0007,.,.;CLNSIG=5,255,255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,.,.;CLNDSDBID=NBK1507:C0587248:218040:3071:309776008,.,.;CLNDBN=Costello syndrome,.,.;CLNACC=RCV000013440.1,.,. +11 534288 rs104894230 C A,G,T . . RSPOS=534288;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000011.9:g.534288C>A,NC_000011.9:g.534288C>G,NC_000011.9:g.534288C>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1,1;CLNSRCID=190020.0001,190020.0004,190020.0013;CLNSIG=255|5|5,5,5|1;CLNDSDB=.|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|NCBI,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,.|.;CLNDSDBID=.|NBK1507:C0587248:218040:3071:309776008|C1968782,NBK1507:C0587248:218040:3071:309776008,.|.;CLNDBN=Bladder cancer\x2c somatic|Costello syndrome|Myopathy\x2c congenital\x2c with excess of muscle spindles,Costello syndrome,Costello syndrome\x2c severe|NEVUS SEBACEOUS\x2c SOMATIC;CLNACC=RCV000013431.1|RCV000013432.1|RCV000013433.1,RCV000013437.1,RCV000013446.1|RCV000029210.1 +11 534289 rs104894229 C A,G,T . . RSPOS=534289;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=HRAS:3265;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000011.9:g.534289C>A,NC_000011.9:g.534289C>G,NC_000011.9:g.534289C>T;CLNSRC=OMIM Allelic Variant,.,OMIM Allelic Variant;CLNORIGIN=1,2,1;CLNSRCID=190020.0014,.,190020.0003;CLNSIG=5|1,255,5|5|255|1;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|.,.,GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|NCBI|.|.;CLNDSDBID=NBK1507:C0587248:218040:3071:309776008|.,.,NBK1507:C0587248:218040:3071:309776008|C1968782|.|.;CLNDBN=Costello syndrome|NEVUS SEBACEOUS\x2c SOMATIC,.,Costello syndrome|Myopathy\x2c congenital\x2c with excess of muscle spindles|EPIDERMAL NEVUS WITH UROTHELIAL CANCER\x2c SOMATIC|NEVUS SEBACEOUS\x2c SOMATIC;CLNACC=RCV000013447.1|RCV000029211.1,.,RCV000013435.1|RCV000013436.1|RCV000022796.1|RCV000029209.1 +11 108170479 rs121434217 G C . . RSPOS=108170479;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=ATM:472;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.108170479G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=607585.0009;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=T-cell prolymphocytic leukemia\x2c somatic;CLNACC=RCV000003165.1 +11 108172506 rs121434223 C G . . RSPOS=108172506;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000601000002110100;GENEINFO=ATM:472;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.108172506C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=607585.0025;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=T-cell prolymphocytic leukemia\x2c somatic;CLNACC=RCV000003183.1 +11 108200960 rs121434220 C T . . RSPOS=108200960;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000601000002110100;GENEINFO=ATM:472;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.108200960C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=607585.0019;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK26468:C0004135:208900:100:68504005;CLNDBN=Ataxia-telangiectasia syndrome;CLNACC=RCV000003175.1 +11 108204652 rs121434218 T C . . RSPOS=108204652;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=ATM:472;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.108204652T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=607585.0011;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Ataxia-telangiectasia without immunodeficiency;CLNACC=RCV000003167.1 +11 108236203 rs121434219 C T . . RSPOS=108236203;dbSNPBuildID=132;SSR=0;SAO=1;VP=050060000601000002110100;GENEINFO=ATM:472;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000011.9:g.108236203C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=607585.0012;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Ataxia-telangiectasia without immunodeficiency;CLNACC=RCV000003168.1 +12 25378562 rs121913527 C T . . RSPOS=25378562;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.25378562C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25378651 rs202247812 T C . . RSPOS=25378651;RV;dbSNPBuildID=136;SSR=0;SAO=1;VP=050068000a05000002110100;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;PMC;NSM;REF;ASP;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25378651T>C;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25380275 rs17851045 T A,G . . RSPOS=25380275;RV;dbSNPBuildID=123;SSR=0;SAO=3;VP=050260000a01000102100120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;GNO;OTHERKG;LSD;CLNALLE=2;CLNHGVS=NC_000012.11:g.25380275T>G;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25380276 rs121913240 T A,C,G . . RSPOS=25380276;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100124;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.25380276T>A,NC_000012.11:g.25380276T>C,NC_000012.11:g.25380276T>G;CLNSRC=.,.,.;CLNORIGIN=2,2,2;CLNSRCID=.,.,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +12 25380277 rs121913238 G C,T . . RSPOS=25380277;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000012.11:g.25380277G>C,NC_000012.11:g.25380277G>T;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +12 25380280 rs104894359 C G,T . . RSPOS=25380280;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000012.11:g.25380280C>G,NC_000012.11:g.25380280C>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=190070.0009,190070.0020;CLNSIG=5,5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT,GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1186:C1275081:115150:1340:403770008,NBK1124:C1860991:609942:648;CLNDBN=Cardio-facio-cutaneous syndrome,Noonan syndrome 3;CLNACC=RCV000013416.1,RCV000013428.1 +12 25380282 rs104886029 G A . . RSPOS=25380282;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25380282G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25380283 rs121913528 C T . . RSPOS=25380283;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25380283C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=190070.0004;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Bladder cancer\x2c transitional cell\x2c somatic;CLNACC=RCV000013410.1 +12 25380285 rs104894364 G A . . RSPOS=25380285;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25380285G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190070.0011;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C1860991:609942:648;CLNDBN=Noonan syndrome 3;CLNACC=RCV000013419.1 +12 25398255 rs121913236 G T . . RSPOS=25398255;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.25398255G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25398262 rs121913538 C A . . RSPOS=25398262;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.25398262C>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 25398279 rs104894365 C T . . RSPOS=25398279;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25398279C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190070.0012;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C1860991:609942:648;CLNDBN=Noonan syndrome 3;CLNACC=RCV000013420.1 +12 25398281 rs112445441 C A,G,T . . RSPOS=25398281;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.25398281C>A,NC_000012.11:g.25398281C>G,NC_000012.11:g.25398281C>T;CLNSRC=.,.,OMIM Allelic Variant;CLNORIGIN=2,2,2;CLNSRCID=.,.,190070.0003;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,Breast adenocarcinoma\x2c somatic;CLNACC=.,.,RCV000013409.1 +12 25398282 rs121913535 C A,G,T . . RSPOS=25398282;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.25398282C>A,NC_000012.11:g.25398282C>G,NC_000012.11:g.25398282C>T;CLNSRC=.,OMIM Allelic Variant,.;CLNORIGIN=2,1,2;CLNSRCID=.,190070.0016,.;CLNSIG=255,255,255;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,Pilocytic astrocytoma\x2c somatic,.;CLNACC=.,RCV000013424.1,. +12 25398284 rs121913529 C A,G,T . . RSPOS=25398284;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.25398284C>A,NC_000012.11:g.25398284C>G,NC_000012.11:g.25398284C>T;CLNSRC=OMIM Allelic Variant,.,OMIM Allelic Variant;CLNORIGIN=1,2,2;CLNSRCID=190070.0006,.,190070.0005;CLNSIG=255|1,255,255|255|255|1|1;CLNDSDB=.|.,.,.|.|.|.|.;CLNDSDBID=.|.,.,.|.|.|.|.;CLNDBN=Pancreatic carcinoma\x2c somatic|NEVUS SEBACEOUS\x2c SOMATIC,.,Pancreatic carcinoma\x2c somatic|Gastric cancer\x2c somatic|Nevus\x2c epidermal\x2c somatic|NEVUS SEBACEOUS\x2c SOMATIC|SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME\x2c SOMATIC MOSAIC;CLNACC=RCV000013413.1|RCV000029216.1,.,RCV000013411.1|RCV000013412.1|RCV000022799.1|RCV000029214.1|RCV000029215.1 +12 25398285 rs121913530 C A,G,T . . RSPOS=25398285;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110124;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.25398285C>A,NC_000012.11:g.25398285C>G,NC_000012.11:g.25398285C>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,2,1;CLNSRCID=190070.0001,190070.0002,190070.0007;CLNSIG=255,255|255,255;CLNDSDB=.,.|.,.;CLNDSDBID=.,.|.,.;CLNDBN=Lung cancer\x2c somatic,Lung cancer\x2c squamous cell\x2c somatic|Bladder cancer\x2c somatic,Gastric cancer\x2c somatic;CLNACC=RCV000013406.1,RCV000013407.1|RCV000013408.1,RCV000013414.1 +12 25398304 rs104894361 T A . . RSPOS=25398304;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25398304T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190070.0017;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1186:C1275081:115150:1340:403770008;CLNDBN=Cardio-facio-cutaneous syndrome;CLNACC=RCV000013425.1 +12 25398306 rs193929331 T C . . RSPOS=25398306;RV;dbSNPBuildID=136;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=KRAS:3845;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.25398306T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190070.0019;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C1860991:609942:648;CLNDBN=Noonan syndrome 3;CLNACC=RCV000013427.1 +12 112888161 rs121918471 TGGT T . . RSPOS=112888162;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002110200;GENEINFO=PTPN11:5781;WGT=1;VC=DIV;PM;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888162_112888164delGGT;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=NBK1124|176876.0024;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648|NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1|Noonan syndrome 1;CLNACC=RCV000014274.1|RCV000014274.1 +12 112888162 rs80338836 GGTG G . . RSPOS=112888163;dbSNPBuildID=131;SSR=0;SAO=0;VP=050168000201000002110200;GENEINFO=PTPN11:5781;WGT=1;VC=DIV;PM;PMC;SLO;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888163_112888165delGTG;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=0;CLNSRCID=NBK1124|176876.0024;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648|NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1|Noonan syndrome 1;CLNACC=RCV000014274.1|RCV000014274.1 +12 112888166 rs121918461 A G . . RSPOS=112888166;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888166A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0010;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014258.1 +12 112888168 rs121918460 T G . . RSPOS=112888168;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888168T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0009;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014257.1 +12 112888172 rs121918459 A G . . RSPOS=112888172;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888172A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0008;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014261.1 +12 112888198 rs121918453 G T . . RSPOS=112888198;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888198G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0001;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014252.1 +12 112888199 rs121918454 C G . . RSPOS=112888199;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888199C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0002;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014253.1 +12 112888202 rs121918462 C T . . RSPOS=112888202;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888202C>T;CLNSRC=OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0011|176876.0013;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet|NCBI:OMIM:Orphanet|GeneReviews:NCBI:OMIM:SNOMED CT;CLNDSDBID=NBK1124:C0041409:163950:648|C0349639:607785:86834|NBK1124:C0028326:163950:205824006;CLNDBN=Noonan syndrome 1|Juvenile myelomonocytic leukemia|Noonan's syndrome;CLNACC=RCV000014262.1|RCV000030619.1|RCV000030619.1 +12 112888210 rs121918464 G A . . RSPOS=112888210;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888210G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0014;CLNSIG=255;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C0349639:607785:86834;CLNDBN=Juvenile myelomonocytic leukemia;CLNACC=RCV000014264.1 +12 112888211 rs121918465 A C,G,T . . RSPOS=112888211;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110104;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000012.11:g.112888211A>C,NC_000012.11:g.112888211A>G,NC_000012.11:g.112888211A>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1,1;CLNSRCID=176876.0017,176876.0016,176876.0015;CLNSIG=255,255,255;CLNDSDB=NCBI:OMIM:Orphanet,NCBI:OMIM:Orphanet,NCBI:OMIM:Orphanet;CLNDSDBID=C0349639:607785:86834,C0349639:607785:86834,C0349639:607785:86834;CLNDBN=Juvenile myelomonocytic leukemia,Juvenile myelomonocytic leukemia,Juvenile myelomonocytic leukemia;CLNACC=RCV000014267.1,RCV000014266.1,RCV000014265.1 +12 112888220 rs121918466 A G . . RSPOS=112888220;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888220A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0018;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014268.1 +12 112888239 rs61736914 C T . . RSPOS=112888239;GMAF=0.0188;dbSNPBuildID=129;SSR=0;SAO=1;VP=05026800030115011e100100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;PMC;S3D;REF;SYN;VLD;G5;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.112888239C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=3;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 112926884 rs121918458 T A . . RSPOS=112926884;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.112926884T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=176876.0007;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1124:C0041409:163950:648;CLNDBN=Noonan syndrome 1;CLNACC=RCV000014260.1 +12 112926909 rs121918470 A C,G . . RSPOS=112926909;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=PTPN11:5781;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000012.11:g.112926909A>C,NC_000012.11:g.112926909A>G;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=176876.0022,176876.0023;CLNSIG=5,5;CLNDSDB=GeneReviews:NCBI,GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1383:C0175704,NBK1124:C0041409:163950:648;CLNDBN=LEOPARD syndrome,Noonan syndrome 1;CLNACC=RCV000014272.1,RCV000014273.1 +12 121431394 rs193922598 C T . . RSPOS=121431394;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268000a01000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121431394C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121431458 rs193922599 AGAA A . . RSPOS=121431462;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060000201000002100200;GENEINFO=HNF1A:6927;WGT=1;VC=DIV;PM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121431462_121431464delGAA;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121431466 rs193922600 C T . . RSPOS=121431466;dbSNPBuildID=136;SSR=0;SAO=1;VP=050260000a01000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121431466C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121431523 rs193922601 C T . . RSPOS=121431523;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060080001000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;INT;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121431523C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121432043 rs193922604 G T . . RSPOS=121432043;dbSNPBuildID=136;SSR=0;SAO=1;VP=050268000a01000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432043G>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121432056 rs193922605 T C . . RSPOS=121432056;dbSNPBuildID=136;SSR=0;SAO=1;VP=050260000a01000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432056T>C;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121432068 rs137853238 G A . . RSPOS=121432068;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432068G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=142410.0005;CLNSIG=5|5;CLNDSDB=NCBI:OMIM|GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C2675866:612520|NBK1518:C0268151:230400:79239:398664009;CLNDBN=Diabetes mellitus\x2c insulin-dependent\x2c 20|Deficiency of UTP-hexose-1-phosphate uridylyltransferase;CLNACC=RCV000016068.1|RCV000022210.1 +12 121432080 rs137853245 C A,G . . RSPOS=121432080;dbSNPBuildID=133;SSR=0;SAO=1;VP=050268000a01000002110100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000012.11:g.121432080C>A,NC_000012.11:g.121432080C>G;CLNSRC=OMIM Allelic Variant,.;CLNORIGIN=1,1;CLNSRCID=142410.0019,.;CLNSIG=5,4;CLNDSDB=NCBI:OMIM:Orphanet,.;CLNDSDBID=C1838100:600496:552,.;CLNDBN=Maturity-onset diabetes of the young\x2c type 3,.;CLNACC=RCV000016083.1,. +12 121432125 rs193922606 C G . . RSPOS=121432125;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060000a01000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432125C>G;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=4;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121432207 rs193922607 C T . . RSPOS=121432207;dbSNPBuildID=136;SSR=0;SAO=1;VP=050060000301000002100100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;REF;SYN;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432207C>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +12 121432208 rs137853240 G A . . RSPOS=121432208;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000a01000002110100;GENEINFO=HNF1A:6927;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000012.11:g.121432208G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=142410.0008;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=DIABETES MELLITUS\x2c TYPE II\x2c SUSCEPTIBILITY TO;CLNACC=RCV000016071.1 +13 28592636 rs121913490 TGAT T . . RSPOS=28592637;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=FLT3:2322;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.28592637_28592639delGAT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 28592637 rs121913232 G C . . RSPOS=28592637;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=FLT3:2322;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.28592637G>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 28592639 rs121913486 TATC T . . RSPOS=28592640;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=FLT3:2322;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.28592640_28592642delATC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 28592640 rs121913487 A T . . RSPOS=28592640;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=FLT3:2322;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.28592640A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 28592641 rs121909646 T A . . RSPOS=28592641;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110120;GENEINFO=FLT3:2322;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.28592641T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=136351.0003;CLNSIG=255|255;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Leukemia\x2c acute myeloid\x2c somatic|Leukemia\x2c acute lymphoblastic\x2c somatic;CLNACC=RCV000017660.1|RCV000017661.1 +13 28592642 rs121913488 C A,G,T . . RSPOS=28592642;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110124;GENEINFO=FLT3:2322;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;OM;NOV;CLNALLE=1,2,3;CLNHGVS=NC_000013.10:g.28592642C>A,NC_000013.10:g.28592642C>G,NC_000013.10:g.28592642C>T;CLNSRC=.,.,.;CLNORIGIN=1,2,1;CLNSRCID=.,.,.;CLNSIG=4,4,4;CLNDSDB=.,.,.;CLNDSDBID=.,.,.;CLNDBN=.,.,.;CLNACC=.,.,. +13 28608341 rs121913491 T C . . RSPOS=28608341;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=FLT3:2322;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.28608341T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 48919244 rs121913296 G T . . RSPOS=48919244;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.48919244G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 48923148 rs121913298 T A . . RSPOS=48923148;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.48923148T>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 48942685 rs121913301 C T . . RSPOS=48942685;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.48942685C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=614041.0008;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1452:C0035335:180200:790;CLNDBN=Retinoblastoma;CLNACC=RCV000013951.1 +13 48955538 rs121913303 C T . . RSPOS=48955538;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.48955538C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 48955550 rs121913304 C T . . RSPOS=48955550;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.48955550C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=614041.0022;CLNSIG=4|1;CLNDSDB=NCBI|NCBI;CLNDSDBID=C0205898|CN069793;CLNDBN=Pineoblastoma|Retinoblastoma\x2c trilateral;CLNACC=RCV000013965.1|RCV000013966.1 +13 49027133 rs137853292 C T . . RSPOS=49027133;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.49027133C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=614041.0004;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1452:C0035335:180200:790;CLNDBN=Retinoblastoma;CLNACC=RCV000013947.1 +13 49027168 rs121913305 C T . . RSPOS=49027168;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.49027168C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 49033842 rs121913299 TCCGG T . . RSPOS=49033843;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=RB1:5925;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.49033843_49033846delCCGG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 49033844 rs137853294 C T . . RSPOS=49033844;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.49033844C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=614041.0019;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1452:C0035335:180200:790;CLNDBN=Retinoblastoma;CLNACC=RCV000013962.1 +13 49033886 rs137853295 G T . . RSPOS=49033886;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.49033886G>T;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=1;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 49037877 rs121913295 G T . . RSPOS=49037877;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000013.10:g.49037877G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +13 49037894 rs137853296 T C . . RSPOS=49037894;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.49037894T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=614041.0024;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1452:C0035335:180200:790;CLNDBN=Retinoblastoma;CLNACC=RCV000013968.1 +13 49039164 rs121913297 G T . . RSPOS=49039164;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=RB1:5925;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000013.10:g.49039164G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=614041.0010;CLNSIG=255;CLNDSDB=NCBI:OMIM:Orphanet;CLNDSDBID=C0149925:182280:70573;CLNDBN=Small cell cancer of the lung;CLNACC=RCV000013953.1 +14 105246551 rs121434592 C T . . RSPOS=105246551;RV;dbSNPBuildID=132;SSR=0;SAO=1;VP=050360000a01000002110100;GENEINFO=AKT1:207;WGT=1;VC=SNV;PM;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000014.8:g.105246551C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164730.0001;CLNSIG=255|255|255|255;CLNDSDB=.|.|.|.;CLNDSDBID=.|.|.|.;CLNDBN=Breast cancer\x2c somatic|Colorectal cancer\x2c somatic|Ovarian cancer\x2c somatic|PROTEUS SYNDROME\x2c SOMATIC;CLNACC=RCV000015017.1|RCV000015018.1|RCV000015019.1|RCV000022675.1 +17 7573996 rs121912662 A G . . RSPOS=7573996;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060800a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;NSM;REF;U3;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7573996A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0031;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013174.1 +17 7574017 rs121912664 C T . . RSPOS=7574017;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060800a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;NSM;REF;U3;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7574017C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0035;CLNSIG=5;CLNDSDB=NCBI;CLNDSDBID=C1859973;CLNDBN=Adrenocortical carcinoma\x2c pediatric;CLNACC=RCV000013178.1 +17 7577022 rs121913344 G A . . RSPOS=7577022;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577022G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7577063 rs121912663 T A . . RSPOS=7577063;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577063T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0034;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013177.1 +17 7577084 rs121912667 T A . . RSPOS=7577084;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577084T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0040;CLNSIG=5|5;CLNDSDB=NCBI|NCBI;CLNDSDBID=C1859973|C0431109;CLNDBN=Adrenocortical carcinoma\x2c pediatric|Choroid plexus carcinoma;CLNACC=RCV000013184.1|RCV000013185.1 +17 7577094 rs28934574 G A . . RSPOS=7577094;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577094G>A;CLNSRC=OMIM Allelic Variant|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0018|191170.0022;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0029463:259500:668:21708004;CLNDBN=Osteosarcoma;CLNACC=RCV000013161.1 +17 7577099 rs121912660 C A,G . . RSPOS=7577099;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000017.10:g.7577099C>A,NC_000017.10:g.7577099C>G;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=.,191170.0024;CLNSIG=0,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,Nasopharyngeal carcinoma\x2c somatic;CLNACC=.,RCV000013167.1 +17 7577120 rs28934576 C T . . RSPOS=7577120;RV;GMAF=0.0005;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000016110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577120C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0020;CLNSIG=5|255;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT|.;CLNDSDBID=NBK1311:C1835398:151623:524:428850001|.;CLNDBN=Li-Fraumeni syndrome 1|Thyroid carcinoma\x2c anaplastic\x2c somatic;CLNACC=RCV000013163.1|RCV000013164.1 +17 7577121 rs121913343 G A . . RSPOS=7577121;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577121G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7577124 rs121912657 C A . . RSPOS=7577124;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577124C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0012;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013152.1 +17 7577141 rs193920774 C T . . RSPOS=7577141;RV;dbSNPBuildID=136;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577141C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7577509 rs121912652 C T . . RSPOS=7577509;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577509C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0002;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013141.1 +17 7577511 rs28934577 A T . . RSPOS=7577511;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577511A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0028;CLNSIG=5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0029463:259500:668:21708004;CLNDBN=Osteosarcoma;CLNACC=RCV000013171.1 +17 7577526 rs121912653 A G . . RSPOS=7577526;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577526A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0004;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013143.1 +17 7577534 rs28934571 C A . . RSPOS=7577534;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577534C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0006;CLNSIG=255|255;CLNDSDB=.|.;CLNDSDBID=.|.;CLNDBN=Hepatocellular carcinoma\x2c somatic|Cervical cancer\x2c somatic;CLNACC=RCV000013145.1|RCV000013146.1 +17 7577538 rs11540652 C T . . RSPOS=7577538;RV;dbSNPBuildID=120;SSR=0;SAO=3;VP=050368000a01000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577538C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=191170.0010;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013150.1 +17 7577539 rs121912651 G A . . RSPOS=7577539;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577539G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0001;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013140.1 +17 7577547 rs121912656 C T . . RSPOS=7577547;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577547C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0009;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013149.1 +17 7577556 rs121912655 C T . . RSPOS=7577556;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577556C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0008;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Ependymoma\x2c intracranial;CLNACC=RCV000013148.1 +17 7577559 rs28934573 G A . . RSPOS=7577559;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577559G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0013;CLNSIG=5|5;CLNDSDB=NCBI|NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=C0206624|C0029463:259500:668:21708004;CLNDBN=Hepatoblastoma|Osteosarcoma;CLNACC=RCV000013153.1|RCV000013154.1 +17 7577567 rs193920789 A C . . RSPOS=7577567;RV;dbSNPBuildID=136;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7577567A>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578190 rs121912666 T G . . RSPOS=7578190;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578190T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0039;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013183.1 +17 7578283 rs121912665 G A . . RSPOS=7578283;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578283G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0038;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1211:CN029768:114500:33402;CLNDBN=Familial colorectal cancer;CLNACC=RCV000013182.1 +17 7578406 rs28934578 C T . . RSPOS=7578406;RV;dbSNPBuildID=132;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578406C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0030;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013173.1 +17 7578449 rs193920817 C T . . RSPOS=7578449;RV;dbSNPBuildID=136;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578449C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=0;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578461 rs121912654 C A . . RSPOS=7578461;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578461C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0007;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Hepatocellular carcinoma\x2c somatic;CLNACC=RCV000013147.1 +17 7578468 rs137852793 G A . . RSPOS=7578468;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000301000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;REF;SYN;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578468G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578470 rs137852789 C T . . RSPOS=7578470;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578470C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578470 rs137852791 CGGGCGGGGGT C . . RSPOS=7578471;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=TP53:7157;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578471_7578480delGGGCGGGGGT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578470 rs137852790 CGGGCGGGGGTGT C . . RSPOS=7578471;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060000001000002100200;GENEINFO=TP53:7157;WGT=1;VC=DIV;PM;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578471_7578482delGGGCGGGGGTGT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578479 rs28934874 G A,T . . RSPOS=7578479;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000017.10:g.7578479G>A,NC_000017.10:g.7578479G>T;CLNSRC=OMIM Allelic Variant,OMIM Allelic Variant;CLNORIGIN=1,1;CLNSRCID=191170.0026,191170.0025;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=Breast cancer\x2c somatic,Breast cancer\x2c somatic;CLNACC=RCV000013169.1,RCV000013168.1 +17 7578515 rs137852794 TG T . . RSPOS=7578517;RV;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002110200;GENEINFO=TP53:7157;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578517delG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7578532 rs28934873 A G . . RSPOS=7578532;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578532A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0011;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1311:C1835398:151623:524:428850001;CLNDBN=Li-Fraumeni syndrome 1;CLNACC=RCV000013151.1 +17 7578544 rs137852792 G A . . RSPOS=7578544;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260400a01000002110120;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSM;REF;U5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7578544G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 7579329 rs121912658 T A . . RSPOS=7579329;RV;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260020601000002110100;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;S3D;NSN;REF;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.7579329T>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0017;CLNSIG=5|5|5;CLNDSDB=NCBI:OMIM:Orphanet:SNOMED CT|NCBI|NCBI;CLNDSDBID=C0029463:259500:668:21708004|C0152013|C0349661;CLNDBN=Osteosarcoma|Adenocarcinoma of lung|Glioma of brain;CLNACC=RCV000013158.1|RCV000013159.1|RCV000013160.1 +17 7579472 rs1042522 G C . . RSPOS=7579472;RV;GMAF=0.3979;dbSNPBuildID=86;SSR=0;SAO=1;VP=050178020a0117051f110101;GENEINFO=TP53:7157;WGT=1;VC=SNV;PM;TPA;PMC;SLO;NSM;REF;R5;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD;OM;GCF;CLNALLE=1;CLNHGVS=NC_000017.10:g.7579472G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=191170.0005;CLNSIG=2;CLNDSDB=.;CLNDSDBID=.;CLNDBN=CODON 72 POLYMORPHISM\x2c (rs1042522);CLNACC=RCV000013144.1 +17 37880218 rs121913469 GTT GCC . . RSPOS=37880219;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002110820;GENEINFO=ERBB2:2064;WGT=1;VC=MNV;PM;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37880219_37880220delinsCC;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164870.0005;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Adenocarcinoma of lung\x2c somatic;CLNACC=RCV000014891.1 +17 37880220 rs121913470 T C . . RSPOS=37880220;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=ERBB2:2064;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.37880220T>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37880261 rs121913468 G C . . RSPOS=37880261;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000a01000002100120;GENEINFO=ERBB2:2064;WGT=1;VC=SNV;PM;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.37880261G>C;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37880997 rs28933369 G A . . RSPOS=37880997;dbSNPBuildID=126;SSR=0;SAO=3;VP=050060020a01000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;NSM;REF;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37880997G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=2;CLNSRCID=164870.0007;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Gastric cancer\x2c somatic;CLNACC=RCV000014893.1 +17 37881000 rs121913471 G T . . RSPOS=37881000;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060020a01000002100120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;NSM;REF;R5;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881000G>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881299 rs104886007 C T . . RSPOS=37881299;dbSNPBuildID=132;SSR=0;SAO=3;VP=0500600a0001000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;INT;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881299C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881314 rs104886008 C T . . RSPOS=37881314;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060020301000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;REF;SYN;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881314C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881328 rs104886011 G A . . RSPOS=37881328;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060020301000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;REF;SYN;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881328G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881343 rs137852788 C T . . RSPOS=37881343;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060020301000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;REF;SYN;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881343C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881376 rs104886009 C T . . RSPOS=37881376;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060020301000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;REF;SYN;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881376C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +17 37881378 rs28933370 A G . . RSPOS=37881378;dbSNPBuildID=126;SSR=0;SAO=1;VP=050060020a01040402110100;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;NSM;REF;R5;VLD;HD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881378A>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=164870.0008;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Ovarian cancer\x2c somatic;CLNACC=RCV000014894.1 +17 37881413 rs104886010 C T . . RSPOS=37881413;dbSNPBuildID=132;SSR=0;SAO=3;VP=050060020301000002110120;GENEINFO=ERBB2:2064|MIR4728:100616132;WGT=1;VC=SNV;PM;REF;SYN;R5;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000017.10:g.37881413C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +18 48591891 rs121912581 G A . . RSPOS=48591891;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48591891G>A;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=JP and JP/HHT;CLNACC=RCV000021707.1 +18 48591909 rs121912576 G T . . RSPOS=48591909;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48591909G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=600993.0001;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Pancreatic carcinoma\x2c somatic;CLNACC=RCV000009062.1 +18 48591918 rs80338963 C T . . RSPOS=48591918;dbSNPBuildID=131;SSR=0;SAO=1;VP=050368000a01000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;PMC;S3D;SLO;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48591918C>T;CLNSRC=GeneReviews|OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=NBK1469|600993.0008;CLNSIG=5|5|5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:Orphanet|.;CLNDSDBID=NBK1469:C0345893:174900:C1868081:2929:9273005|NBK1351:C1832942:175050:2929|.;CLNDBN=Juvenile polyposis syndrome|Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome|JP\x2c JP/HHT\x2c and HHT;CLNACC=RCV000009071.1|RCV000009072.1|RCV000021711.1 +18 48593406 rs121912580 G A . . RSPOS=48593406;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48593406G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=600993.0010;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet;CLNDSDBID=NBK1351:C1832942:175050:2929;CLNDBN=Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome;CLNACC=RCV000009074.1 +18 48593411 rs80338964 C T . . RSPOS=48593411;dbSNPBuildID=131;SSR=0;SAO=1;VP=050368000601000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;PMC;S3D;SLO;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48593411C>T;CLNSRC=GeneReviews;CLNORIGIN=0;CLNSRCID=NBK1469;CLNSIG=5|5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:SNOMED CT|GeneReviews:NCBI:OMIM:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1469:C0345893:174900:C1868081:2929:9273005|NBK1469:C0345893:174900:C1868081:2929:9273005;CLNDBN=Juvenile polyposis syndrome|Juvenile polyposis syndrome;CLNACC=RCV000020633.1|RCV000021723.1 +18 48593485 rs121912577 C G . . RSPOS=48593485;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48593485C>G;CLNSRC=.;CLNORIGIN=1;CLNSRCID=.;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1469:C0345893:174900:C1868081:2929:9273005;CLNDBN=Juvenile polyposis syndrome;CLNACC=RCV000021726.1 +18 48593492 rs80338965 GACAG G . . RSPOS=48593493;dbSNPBuildID=131;SSR=0;SAO=0;VP=050168001201000002110200;GENEINFO=SMAD4:4089;WGT=1;VC=DIV;PM;PMC;SLO;NSF;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48593493_48593496delACAG;CLNSRC=GeneReviews;CLNORIGIN=0;CLNSRCID=NBK1469;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1469:C0345893:174900:C1868081:2929:9273005;CLNDBN=Juvenile polyposis syndrome;CLNACC=RCV000020634.1 +18 48604655 rs121912578 G C . . RSPOS=48604655;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48604655G>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=600993.0003;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Pancreatic carcinoma\x2c somatic;CLNACC=RCV000009064.1 +18 48604721 rs121912579 A T . . RSPOS=48604721;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=SMAD4:4089;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000018.9:g.48604721A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=600993.0004;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Pancreatic carcinoma\x2c somatic;CLNACC=RCV000009065.1 +19 1207020 rs137853079 C A . . RSPOS=1207020;dbSNPBuildID=133;SSR=0;SAO=1;VP=050060000601000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207020C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0015;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Pancreatic cancer\x2c sporadic;CLNACC=RCV000007878.1 +19 1207021 rs121913324 C T . . RSPOS=1207021;dbSNPBuildID=133;SSR=0;SAO=3;VP=050060000601000002100120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207021C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1207057 rs137853080 T G . . RSPOS=1207057;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207057T>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0019;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Melanoma\x2c sporadic malignant;CLNACC=RCV000007882.1 +19 1207076 rs121913319 TG T . . RSPOS=1207081;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=STK11:6794;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207081delG;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1207081 rs137854584 G T . . RSPOS=1207081;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207081G>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0010;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1266:C0031269:175200:2869:54411001;CLNDBN=Peutz-Jeghers syndrome;CLNACC=RCV000007873.1 +19 1207112 rs137853077 T C . . RSPOS=1207112;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000a01000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207112T>C;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0008;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1266:C0031269:175200:2869:54411001;CLNDBN=Peutz-Jeghers syndrome;CLNACC=RCV000007871.1 +19 1207162 rs137853076 A T . . RSPOS=1207162;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1207162A>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0006;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1266:C0031269:175200:2869:54411001;CLNDBN=Peutz-Jeghers syndrome;CLNACC=RCV000007869.1 +19 1220487 rs121913315 G A,T . . RSPOS=1220487;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002110120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;OM;CLNALLE=1,2;CLNHGVS=NC_000019.9:g.1220487G>A,NC_000019.9:g.1220487G>T;CLNSRC=.,OMIM Allelic Variant;CLNORIGIN=2,1;CLNSRCID=.,602216.0013;CLNSIG=255,5;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,Melanoma\x2c sporadic malignant;CLNACC=.,RCV000007876.1 +19 1220488 rs121913316 A T . . RSPOS=1220488;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1220488A>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1220502 rs121913317 G A,T . . RSPOS=1220502;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000e01000002100120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;NSN;REF;OTHERKG;LSD;CLNALLE=1,2;CLNHGVS=NC_000019.9:g.1220502G>A,NC_000019.9:g.1220502G>T;CLNSRC=.,.;CLNORIGIN=2,2;CLNSRCID=.,.;CLNSIG=255,255;CLNDSDB=.,.;CLNDSDBID=.,.;CLNDBN=.,.;CLNACC=.,. +19 1221236 rs137853075 C A . . RSPOS=1221236;dbSNPBuildID=133;SSR=0;SAO=1;VP=050260000601000002110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1221236C>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0002;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1266:C0031269:175200:2869:54411001;CLNDBN=Peutz-Jeghers syndrome;CLNACC=RCV000007865.1 +19 1221263 rs121913320 GTTGT G . . RSPOS=1221264;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=STK11:6794;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1221264_1221267delTTGT;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1221313 rs121913321 GC G . . RSPOS=1221319;dbSNPBuildID=133;SSR=0;SAO=0;VP=050060001201000002100200;GENEINFO=STK11:6794;WGT=1;VC=DIV;PM;NSF;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1221319delC;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1221319 rs121913322 C T . . RSPOS=1221319;GMAF=0.0018;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000016100120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSM;REF;KGPhase1;KGPROD;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1221319C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1223059 rs121913325 G A . . RSPOS=1223059;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002100120;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.1223059G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 1223125 rs59912467 C G . . RSPOS=1223125;GMAF=0.0128;dbSNPBuildID=129;SSR=0;SAO=1;VP=050060000a01170416110100;GENEINFO=STK11:6794;WGT=1;VC=SNV;PM;NSM;REF;VLD;G5A;G5;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000019.9:g.1223125C>G;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=602216.0024;CLNSIG=5;CLNDSDB=GeneReviews:NCBI:OMIM:Orphanet:SNOMED CT;CLNDSDBID=NBK1266:C0031269:175200:2869:54411001;CLNDBN=Peutz-Jeghers syndrome;CLNACC=RCV000007887.1 +19 17945696 rs3213409 C T . . RSPOS=17945696;RV;GMAF=0.0037;dbSNPBuildID=106;SSR=0;SAO=3;VP=050268000a01050517100121;GENEINFO=JAK3:3718;WGT=1;VC=SNV;PM;PMC;S3D;NSM;REF;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD;GCF;CLNALLE=1;CLNHGVS=NC_000019.9:g.17945696C>T;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +19 17948009 rs121913504 G A . . RSPOS=17948009;RV;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000a01000002100120;GENEINFO=JAK3:3718;WGT=1;VC=SNV;PM;S3D;NSM;REF;OTHERKG;LSD;CLNALLE=1;CLNHGVS=NC_000019.9:g.17948009G>A;CLNSRC=.;CLNORIGIN=2;CLNSRCID=.;CLNSIG=255;CLNDSDB=.;CLNDSDBID=.;CLNDBN=.;CLNACC=. +20 36031762 rs121913314 C T . . RSPOS=36031762;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260000601000002110120;GENEINFO=SRC:6714;WGT=1;VC=SNV;PM;S3D;NSN;REF;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000020.10:g.36031762C>T;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=190090.0001;CLNSIG=5;CLNDSDB=.;CLNDSDBID=.;CLNDBN=Colon cancer\x2c advanced;CLNACC=RCV000013401.1 +20 57484421 rs121913495 G A . . RSPOS=57484421;dbSNPBuildID=133;SSR=0;SAO=3;VP=050260800a01000002110120;GENEINFO=GNAS:2778;WGT=1;VC=SNV;PM;S3D;NSM;REF;U3;OTHERKG;LSD;OM;CLNALLE=1;CLNHGVS=NC_000020.10:g.57484421G>A;CLNSRC=OMIM Allelic Variant;CLNORIGIN=1;CLNSRCID=139320.0009;CLNSIG=255|255|255|255;CLNDSDB=NCBI|.|.|.;CLNDSDBID=CN071115|.|.|.;CLNDBN=McCune-Albright syndrome\x2c somatic\x2c mosaic|Pituitary tumor\x2c growth hormone-secreting\x2c somatic|Acth-independent macronodular adrenal hyperplasia\x2c somatic|Sex cord stromal tumor\x2c somatic;CLNACC=RCV000017290.1|RCV000017291.1|RCV000017292.1|RCV000017293.1
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool-data/GALAXY_TSACP.bed Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,221 @@ +chr1 43814981 43815163 MPL1_2.chr1.43815008.43815009_tile_1 100 + 43815005 43815137 +chr1 115256499 115256680 NRAS1_7.chr1.115256528.115256531_tile_1 100 + 115256525 115256653 +chr1 115258701 115258884 NRAS8_13.chr1.115258730.115258748_tile_1 100 + 115258727 115258855 +chr2 29432635 29432822 ALK1.chr2.29432664.29432664_tile_1 100 + 29432662 29432795 +chr2 29443666 29443836 ALK2.chr2.29443695.29443695_tile_1 100 + 29443691 29443810 +chr2 209113083 209113264 IDH1_1_2.chr2.209113112.209113113_tile_1 100 + 209113110 209113237 +chr2 212288911 212289100 ERBB4_1_2.chr2.212288942.212288955_tile_1 100 + 212288938 212289073 +chr2 212530035 212530210 ERBB4_3_4.chr2.212530066.212530135_tile_1 100 + 212530061 212530183 +chr2 212576820 212576990 ERBB4_5.chr2.212576857.212576857_tile_1 100 + 212576850 212576960 +chr2 212578314 212578499 ERBB4_6_7.chr2.212578341.212578349_tile_1 100 + 212578339 212578470 +chr2 212587114 212587285 ERBB4_8.chr2.212587147.212587147_tile_1 100 + 212587141 212587258 +chr2 212589782 212589957 ERBB4_9.chr2.212589811.212589811_tile_1 100 + 212589809 212589930 +chr2 212652705 212652876 ERBB4_10.chr2.212652764.212652764_tile_1 100 + 212652735 212652849 +chr2 212812126 212812311 ERBB4_11.chr2.212812157.212812157_tile_1 100 + 212812155 212812284 +chr3 10183768 10183952 VHL1_2.chr3.10183797.10183817_tile_1 100 + 10183793 10183926 +chr3 10188216 10188401 VHL3_5.chr3.10188245.10188301_tile_1 100 + 10188243 10188374 +chr3 10191449 10191634 VHL6_8.chr3.10191480.10191506_tile_1 100 + 10191477 10191607 +chr3 37067211 37067394 MLH1.chr3.37067240.37067240_tile_1 100 + 37067237 37067367 +chr3 41266009 41266180 CTNNB1_1_16.chr3.41266040.41266137_tile_1 100 + 41266036 41266153 +chr3 178916835 178917024 PIK3CA1.chr3.178916876.178916876_tile_1 100 + 178916861 178916997 +chr3 178921524 178921709 PIK3CA2.chr3.178921553.178921553_tile_1 100 + 178921551 178921682 +chr3 178927905 178928082 PIK3CA3.chr3.178927980.178927980_tile_1 100 + 178927932 178928055 +chr3 178936043 178936214 PIK3CA4_11.chr3.178936074.178936095_tile_1 100 + 178936070 178936187 +chr3 178938831 178939004 PIK3CA12.chr3.178938860.178938860_tile_1 100 + 178938858 178938977 +chr3 178951880 178952054 PIK3CA13_20.chr3.178952007.178952150_tile_1 100 + 178951906 178952026 +chr3 178951998 178952184 PIK3CA13_20.chr3.178952007.178952150_tile_2 100 - 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89717637 89717772 +chr10 89720683 89720870 PTEN13.chr10.89720716.89720852_tile_1 100 + 89720708 89720843 +chr10 89720813 89720991 PTEN13.chr10.89720716.89720852_tile_2 100 - 89720842 89720961 +chr10 123258005 123258184 FGFR2_1.chr10.123258034.123258034_tile_1 100 + 123258032 123258157 +chr10 123274745 123274930 FGFR2_2.chr10.123274774.123274803_tile_1 100 + 123274772 123274903 +chr10 123279384 123279555 FGFR2_5.chr10.123279503.123279677_tile_1 100 + 123279411 123279528 +chr10 123279470 123279640 FGFR2_5.chr10.123279503.123279677_tile_2 100 - 123279498 123279614 +chr10 123279586 123279769 FGFR2_5.chr10.123279503.123279677_tile_3 100 + 123279613 123279742 +chr11 533842 534021 HRAS1.chr11.533873.533875_tile_1 100 + 533868 533994 +chr11 534250 534434 HRAS6.chr11.534285.534289_tile_1 100 + 534277 534410 +chr11 108117816 108117989 ATM1.chr11.108117847.108117848_tile_1 100 + 108117845 108117962 +chr11 108119792 108119963 ATM2.chr11.108119823.108119823_tile_1 100 + 108119819 108119936 +chr11 108123512 108123683 ATM3.chr11.108123551.108123551_tile_1 100 + 108123541 108123654 +chr11 108137938 108138126 ATM4.chr11.108137973.108138003_tile_1 100 + 108137967 108138096 +chr11 108155103 108155281 ATM6.chr11.108155132.108155132_tile_1 100 + 108155130 108155251 +chr11 108170441 108170618 ATM7.chr11.108170476.108170479_tile_1 100 + 108170468 108170591 +chr11 108172390 108172571 ATM9.chr11.108172421.108172421_tile_1 100 + 108172417 108172544 +chr11 108173611 108173801 ATM10.chr11.108173640.108173640_tile_1 100 + 108173635 108173771 +chr11 108180914 108181101 ATM11.chr11.108180945.108180945_tile_1 100 + 108180942 108181074 +chr11 108200925 108201096 ATM12.chr11.108200958.108200961_tile_1 100 + 108200954 108201069 +chr11 108204650 108204823 ATM14.chr11.108204681.108204681_tile_1 100 + 108204679 108204796 +chr11 108205738 108205928 ATM15.chr11.108205769.108205769_tile_1 100 + 108205766 108205900 +chr11 108206565 108206750 ATM16.chr11.108206594.108206594_tile_1 100 + 108206592 108206723 +chr11 108218060 108218247 ATM17.chr11.108218089.108218089_tile_1 100 + 108218087 108218220 +chr11 108225561 108225751 ATM18.chr11.108225590.108225590_tile_1 100 + 108225588 108225725 +chr11 108236057 108236241 ATM19.chr11.108236086.108236203_tile_1 100 + 108236084 108236215 +chr12 25378531 25378717 KRAS1.chr12.25378562.25378562_tile_1 100 + 25378558 25378689 +chr12 25380244 25380427 KRAS2.chr12.25380275.25380283_tile_1 100 + 25380270 25380398 +chr12 25398224 25398414 KRAS7.chr12.25398255.25398285_tile_1 100 + 25398253 25398386 +chr12 112888134 112888323 PTPN11_1.chr12.112888163.112888211_tile_1 100 + 112888160 112888296 +chr12 112926855 112927032 PTPN11_10.chr12.112926884.112926888_tile_1 100 + 112926881 112927005 +chr12 121431384 121431558 HNF1A_1.chr12.121431413.121431414_tile_1 100 + 121431410 121431532 +chr12 121432041 121432221 HNF1A_3.chr12.121432070.121432070_tile_1 100 + 121432065 121432195 +chr13 28592589 28592766 FLT3_1.chr13.28592620.28592653_tile_1 100 + 28592617 28592739 +chr13 28602294 28602464 FLT3_13.chr13.28602329.28602329_tile_1 100 + 28602320 28602436 +chr13 28608213 28608402 FLT3_14.chr13.28608244.28608341_tile_1 100 + 28608242 28608375 +chr13 28610097 28610267 FLT3_22.chr13.28610138.28610138_tile_1 100 - 28610122 28610239 +chr13 48919155 48919336 RB1_1.chr13.48919244.48919244_tile_1 100 + 48919185 48919309 +chr13 48923119 48923296 RB1_2.chr13.48923148.48923148_tile_1 100 + 48923146 48923269 +chr13 48942654 48942826 RB1_3.chr13.48942685.48942685_tile_1 100 + 48942683 48942798 +chr13 48955503 48955684 RB1_4.chr13.48955538.48955550_tile_1 100 + 48955532 48955657 +chr13 49027111 49027288 RB1_6.chr13.49027168.49027168_tile_1 100 + 49027140 49027261 +chr13 49033812 49033989 RB1_7.chr13.49033843.49033846_tile_1 100 + 49033839 49033962 +chr13 49037814 49037985 RB1_8.chr13.49037877.49037877_tile_1 100 + 49037844 49037958 +chr13 49039131 49039304 RB1_9.chr13.49039164.49039164_tile_1 100 + 49039158 49039277 +chr14 105246428 105246600 AKT1.chr14.105246455.105246455_tile_1 100 + 105246452 105246574 +chr16 68835612 68835782 CDH1_1.chr16.68835649.68835650_tile_1 100 + 68835638 68835760 +chr16 68846108 68846283 CDH1_2.chr16.68846137.68846137_tile_1 100 + 68846135 68846256 +chr16 68847245 68847422 CDH1_3.chr16.68847274.68847277_tile_1 100 + 68847272 68847395 +chr17 7573976 7574147 TP53_1.chr17.7574003.7574021_tile_1 100 + 7574001 7574120 +chr17 7576995 7577166 TP53_3.chr17.7577022.7577129_tile_1 100 + 7577020 7577139 +chr17 7577494 7577683 TP53_17.chr17.7577523.7577574_tile_1 100 + 7577521 7577656 +chr17 7578063 7578234 TP53_31_59.chr17.7578190.7578536_tile_1 100 + 7578091 7578207 +chr17 7578155 7578325 TP53_31_59.chr17.7578190.7578536_tile_2 100 - 7578180 7578303 +chr17 7578245 7578415 TP53_31_59.chr17.7578190.7578536_tile_3 100 + 7578273 7578389 +chr17 7578345 7578515 TP53_31_59.chr17.7578190.7578536_tile_4 100 - 7578373 7578491 +chr17 7578467 7578645 TP53_31_59.chr17.7578190.7578536_tile_5 100 + 7578490 7578619 +chr17 7579323 7579507 TP53_60.chr17.7579358.7579403_tile_1 100 + 7579350 7579481 +chr17 7579851 7580032 TP53_64.chr17.7579882.7579882_tile_1 100 + 7579878 7580005 +chr17 37880190 37880361 ERBB2_1.chr17.37880219.37880261_tile_1 100 + 37880216 37880334 +chr17 37880962 37881151 ERBB2_4.chr17.37880993.37881012_tile_1 100 + 37880986 37881124 +chr17 37881297 37881482 ERBB2_13.chr17.37881332.37881440_tile_1 100 + 37881324 37881455 +chr18 48575130 48575301 SMAD4_1.chr18.48575169.48575170_tile_1 100 + 48575160 48575272 +chr18 48581167 48581346 SMAD4_2.chr18.48581198.48581198_tile_1 100 + 48581195 48581319 +chr18 48584527 48584714 SMAD4_3.chr18.48584560.48584560_tile_1 100 + 48584553 48584687 +chr18 48586233 48586416 SMAD4_4.chr18.48586262.48586262_tile_1 100 + 48586260 48586389 +chr18 48591795 48591982 SMAD4_5.chr18.48591826.48591919_tile_1 100 + 48591822 48591955 +chr18 48593376 48593547 SMAD4_11.chr18.48593405.48593405_tile_1 100 + 48593402 48593520 +chr18 48602997 48603168 SMAD4_12.chr18.48603032.48603094_tile_1 100 + 48603025 48603139 +chr18 48604637 48604808 SMAD4_15.chr18.48604668.48604754_tile_1 100 + 48604663 48604781 +chr19 1206992 1207169 STK11_1.chr19.1207021.1207092_tile_1 100 + 1207019 1207142 +chr19 1220458 1220638 STK11_4.chr19.1220487.1220502_tile_1 100 + 1220484 1220614 +chr19 1221231 1221407 STK11_8.chr19.1221264.1221319_tile_1 100 - 1221259 1221381 +chr19 1223034 1223221 STK11_12.chr19.1223059.1223125_tile_1 100 + 1223057 1223196 +chr19 17945665 17945840 JAK3_1.chr19.17945696.17945696_tile_1 100 + 17945690 17945813 +chr19 17947980 17948169 JAK3_2.chr19.17948009.17948009_tile_1 100 + 17948004 17948142 +chr20 36031733 36031923 SRC.chr20.36031762.36031762_tile_1 100 + 36031760 36031895 +chr20 57484389 57484560 GNAS1.chr20.57484420.57484421_tile_1 100 + 57484416 57484533 +chr22 24133938 24134126 SMARCB1_1.chr22.24133967.24133990_tile_1 100 + 24133964 24134100 +chr22 24143209 24143383 SMARCB1_3.chr22.24143240.24143240_tile_1 100 + 24143235 24143357 +chr22 24145551 24145726 SMARCB1_4.chr22.24145582.24145582_tile_1 100 + 24145577 24145699 +chr22 24176323 24176495 SMARCB1_5_6.chr22.24176352.24176357_tile_1 100 + 24176350 24176469 +chr19 3114823 3115004 GNA11_4.chr19.3114942.3115070_tile_1 100 - 3114845 3114981 +chr19 3114957 3115133 GNA11_4.chr19.3114942.3115070_tile_2 100 + 3114980 3115111 +chr19 3118801 3118989 GNA11_5.chr19.3118922.3119051_tile_1 100 - 3118825 3118963 +chr19 3119207 3119395 GNA11_6.chr19.3119204.3119357_tile_2 100 - 3119232 3119373 +chr19 3120864 3121035 GNA11_7.chr19.3120987.3121177_tile_1 100 + 3120887 3121008 +chr19 3120984 3121170 GNA11_7.chr19.3120987.3121177_tile_2 100 - 3121006 3121144 +chr19 3121120 3121304 GNA11_7.chr19.3120987.3121177_tile_3 100 + 3121143 3121280 +chr9 80412405 80412592 GNAQ_4.chr9.80412436.80412564_tile_1 100 + 80412432 80412565 +chr9 80409248 80409421 GNAQ_5.chr9.80409379.80409508_tile_1 100 + 80409278 80409392 +chr9 80409334 80409510 GNAQ_5.chr9.80409379.80409508_tile_2 100 - 80409364 80409486 +chr9 80409458 80409639 GNAQ_5.chr9.80409379.80409508_tile_3 100 + 80409485 80409612 +chr9 80343305 80343476 GNAQ_6.chr9.80343430.80343583_tile_1 100 + 80343330 80343447 +chr9 80343391 80343561 GNAQ_6.chr9.80343430.80343583_tile_2 100 - 80343417 80343531 +chr9 80343503 80343689 GNAQ_6.chr9.80343430.80343583_tile_3 100 + 80343530 80343659 +chr9 80336109 80336280 GNAQ_7.chr9.80336240.80336429_tile_1 100 + 80336139 80336255 +chr9 80336203 80336374 GNAQ_7.chr9.80336240.80336429_tile_2 100 - 80336228 80336347 +chr9 80336319 80336495 GNAQ_7.chr9.80336240.80336429_tile_3 100 + 80336346 80336467 +chr22 17052963 17053133 PIK3CA4_11.chr3.178936074.178936095_tile_1 100 + 17052990 17053106 +chr22 17055412 17055585 PIK3CA12.chr3.178938860.178938860_tile_1 100 + 17055439 17055558 +chr9 33675956 33676480 PTEN7.chr10.89717615.89717772_tile_1 100 - 33675986 33676451 +chr9 33675628 33675815 PTEN13.chr10.89720716.89720852_tile_1 100 - 33675655 33675790 +chr7 65970149 65970483 GNA11_6.chr19.3119204.3119357_tile_2 100 + 65970175 65970458 +chr7 65970284 65970719 GNA11_7.chr19.3120987.3121177_tile_1 100 - 65970311 65970696 +chr2 132181237 132181750 GNAQ_5.chr9.80409379.80409508_tile_1 100 + 132181267 132181721 +chr2 132181447 132181600 GNAQ_6.chr9.80343430.80343583_tile_1 100 + 132181474 132181571 +chr2 132181331 132181839 GNAQ_7.chr9.80336240.80336429_tile_2 100 - 132181356 132181815
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool-data/GALAXY_TruSeq_Amplicon_Cancer_Panel_Manifest_AFP1_PN15032433.txt Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,445 @@ +[Header] +Customer Name "ILLUMINA, INC." +Product Type 15032433 +Date Manufactured +Lot +DesignStudio ID NA +Target Plexity 212 + +[Probes] +Target Region Name Target Region ID Target ID Species Build ID Chromosome Start Position End Position Submitted Target Region Strand ULSO Sequence ULSO Genomic Hits DLSO Sequence DLSO Genomic Hits Probe Strand Designer Design Score Expected Amplifed Region Size SNP Masking Labels +MPL1_2 MPL1_2.chr1.43815008.43815009 MPL1_2.chr1.43815008.43815009_tile_1 Homo sapiens hg19 chr1 43815008 43815009 - AAGTGGCGAAGCCGTAGGTGCGCACG 0 TCAGCAGCAGCAGGCCCAGGACGG 0 - ILLUMINA NA 183 TRUE +NRAS1_7 NRAS1_7.chr1.115256528.115256531 NRAS1_7.chr1.115256528.115256531_tile_1 Homo sapiens hg19 chr1 115256528 115256531 - CAATAGCATTGCATTCCCTGTGGTTTT 0 AGAGTACAGTGCCATGAGAGACCAAT 0 - ILLUMINA NA 182 TRUE +NRAS8_13 NRAS8_13.chr1.115258730.115258748 NRAS8_13.chr1.115258730.115258748_tile_1 Homo sapiens hg19 chr1 115258730 115258748 - GGGTTTTCATTTCCATTGATTATAGAAAG 0 CTGACAATCCAGCTAATCCAGAACCA 0 - ILLUMINA NA 184 TRUE +ALK1 ALK1.chr2.29432664.29432664 ALK1.chr2.29432664.29432664_tile_1 Homo sapiens hg19 chr2 29432664 29432664 - GATAAAATCCTAGTGATGGCCGTTGTA 0 GACATCTACAGGTGAGTAAAGACTGCC 0 - ILLUMINA NA 188 TRUE +ALK2 ALK2.chr2.29443695.29443695 ALK2.chr2.29443695.29443695_tile_1 Homo sapiens hg19 chr2 29443695 29443695 - TGCTGCCCATGTTTACAGAATGCCTT 0 CACCAGAACATTGTTCGCTGCATTG 0 - ILLUMINA NA 171 TRUE +IDH1_1_2 IDH1_1_2.chr2.209113112.209113113 IDH1_1_2.chr2.209113112.209113113_tile_1 Homo sapiens hg19 chr2 209113112 209113113 - GAGGGTTGAGGAGTTCAAGTTGAAACA 0 CATGCTTATGGGGATCAAGTAAGTCAT 0 - ILLUMINA NA 182 TRUE +ERBB4_1_2 ERBB4_1_2.chr2.212288942.212288955 ERBB4_1_2.chr2.212288942.212288955_tile_1 Homo sapiens hg19 chr2 212288942 212288955 - ACTACTGGTATAGTGCTGGTTTGTTCA 0 AGAACGTTTGCCTCAGCCTCCCATCTG 0 - ILLUMINA NA 190 TRUE +ERBB4_3_4 ERBB4_3_4.chr2.212530066.212530135 ERBB4_3_4.chr2.212530066.212530135_tile_1 Homo sapiens hg19 chr2 212530066 212530135 - CATTTCAGGGTCCTGACAACTGTACAA 0 AACTGCACCCAAGGGTAAGCATTCTT 0 - ILLUMINA NA 176 TRUE +ERBB4_5 ERBB4_5.chr2.212576857.212576857 ERBB4_5.chr2.212576857.212576857_tile_1 Homo sapiens hg19 chr2 212576857 212576857 - ATACTCTGCTATTTTATAATGAAGATGCAA 0 CCAGTAACATTGACAAATTCATAAACTGTA 0 - ILLUMINA NA 171 TRUE +ERBB4_6_7 ERBB4_6_7.chr2.212578341.212578349 ERBB4_6_7.chr2.212578341.212578349_tile_1 Homo sapiens hg19 chr2 212578341 212578349 - AGGGTAAGATACATAAACACTATCAATGA 0 TGCCTGCCCTAGTTCCAAGATGGAA 0 - ILLUMINA NA 186 TRUE +ERBB4_8 ERBB4_8.chr2.212587147.212587147 ERBB4_8.chr2.212587147.212587147_tile_1 Homo sapiens hg19 chr2 212587147 212587147 - TGAAAGTAATATTTGCTGTGTTGCAGG 0 CATTCTGTGTCAAGAAATGTCCACGTA 0 - ILLUMINA NA 172 TRUE +ERBB4_9 ERBB4_9.chr2.212589811.212589811 ERBB4_9.chr2.212589811.212589811_tile_1 Homo sapiens hg19 chr2 212589811 212589811 - GCAGACTTTGATCATGGTCCTATCTCT 0 GACTGCTTTGTATGTCTGTGATTTCTC 0 - ILLUMINA NA 176 TRUE +ERBB4_10 ERBB4_10.chr2.212652764.212652764 ERBB4_10.chr2.212652764.212652764_tile_1 Homo sapiens hg19 chr2 212652764 212652764 - AATGGTGGAGTCTATGTAGACCAGAAC 0 TCTTTTTAATTTCTCAAAATGTTCTACCCT 0 - ILLUMINA NA 172 TRUE +ERBB4_11 ERBB4_11.chr2.212812157.212812157 ERBB4_11.chr2.212812157.212812157_tile_1 Homo sapiens hg19 chr2 212812157 212812157 - GTGGCTCTTAATCAGTTTCGTTACCTG 0 GGTAAGGAATATATCCAAAATGGCAAATA 0 - ILLUMINA NA 186 TRUE +VHL1_2 VHL1_2.chr3.10183797.10183817 VHL1_2.chr3.10183797.10183817_tile_1 Homo sapiens hg19 chr3 10183797 10183817 - AAAATGGACCCCGGGGCGGTAGAGGG 0 ATACGGGCAGCACGACGCGCGGACT 0 - ILLUMINA NA 185 TRUE +VHL3_5 VHL3_5.chr3.10188245.10188301 VHL3_5.chr3.10188245.10188301_tile_1 Homo sapiens hg19 chr3 10188245 10188301 - GAACTGGGCTTAATTTTTCAAGTGGTC 0 AGAAGCCCATCGTGTGTCCCTGCATCT 0 - ILLUMINA NA 186 TRUE +VHL6_8 VHL6_8.chr3.10191480.10191506 VHL6_8.chr3.10191480.10191506_tile_1 Homo sapiens hg19 chr3 10191480 10191506 - TTGATGTGCAATGCGCTCCTGTGTCAG 0 GTATACACTGGAAGGGCAAAAACCAAAT 0 - ILLUMINA NA 186 TRUE +MLH1 MLH1.chr3.37067240.37067240 MLH1.chr3.37067240.37067240_tile_1 Homo sapiens hg19 chr3 37067240 37067240 - TGGGAGTTCAAGCATCTCCTCATCTTG 0 ATCTGGTGGGCATAGACCTTATCACT 0 - ILLUMINA NA 184 TRUE +CTNNB1_1_16 CTNNB1_1_16.chr3.41266040.41266137 CTNNB1_1_16.chr3.41266040.41266137_tile_1 Homo sapiens hg19 chr3 41266040 41266137 - GGTATCCACATCCTCTTCCTCAGGATT 0 GTCCAACTCCATCAAATCAGCTATAAA 0 - ILLUMINA NA 172 TRUE +PIK3CA1 PIK3CA1.chr3.178916876.178916876 PIK3CA1.chr3.178916876.178916876_tile_1 Homo sapiens hg19 chr3 178916876 178916876 - AGGGACAACAGTTAAGCTTTATGGTTA 0 AAAAATTCTTCCCTTTCTGCTTCTTG 0 - ILLUMINA NA 190 TRUE +PIK3CA2 PIK3CA2.chr3.178921553.178921553 PIK3CA2.chr3.178921553.178921553_tile_1 Homo sapiens hg19 chr3 178921553 178921553 - ACATTCGGAGATTTGGATGTTCTCCTA 0 TCACGTAGGTTGCACAAAGAATTTTTA 0 - ILLUMINA NA 186 TRUE +PIK3CA3 PIK3CA3.chr3.178927980.178927980 PIK3CA3.chr3.178927980.178927980_tile_1 Homo sapiens hg19 chr3 178927980 178927980 - CTTCTAATCCATGAGGTACTGGCCAAA 0 AACACATTTCAAAACACTTTTCTTCCC 0 - ILLUMINA NA 178 TRUE +PIK3CA4_11 PIK3CA4_11.chr3.178936074.178936095 PIK3CA4_11.chr3.178936074.178936095_tile_1 Homo sapiens hg19 chr3 178936074 178936095 - GGTATGGTAAAAACATGCTGAGATCAG 0 CTCGTGTAGAAATTGCTTTGAGCTGTT 0 - ILLUMINA NA 172 TRUE +PIK3CA12 PIK3CA12.chr3.178938860.178938860 PIK3CA12.chr3.178938860.178938860_tile_1 Homo sapiens hg19 chr3 178938860 178938860 - TAAACAACTCTGCCCCACTGCAGTGAA 0 CTTCAAATACATCCCACATGCACGACA 0 - ILLUMINA NA 174 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_1 Homo sapiens hg19 chr3 178952007 178952150 - CCAAAGCCTCTTGCTCAGTTTTATCTAA 0 AGCCTTGTAACACATCTCCTGAAACC 0 - ILLUMINA NA 175 TRUE +PIK3CA13_20 PIK3CA13_20.chr3.178952007.178952150 PIK3CA13_20.chr3.178952007.178952150_tile_2 Homo sapiens hg19 chr3 178952007 178952150 + CATTGCATACATTCGAAAGACCCTAGC 0 AGATAACTGAGAAAATGAAAGCTCACTCTG 0 + ILLUMINA NA 187 TRUE +FGFR3_1_2 FGFR3_1_2.chr4.1803564.1803568 FGFR3_1_2.chr4.1803564.1803568_tile_1 Homo sapiens hg19 chr4 1803564 1803568 - TTGCTGCCATTCACCTCCACGTGCTTG 0 TCTGTGGGGGCAGATGACGCTCAGG 0 - ILLUMINA NA 176 TRUE +FGFR3_3_4 FGFR3_3_4.chr4.1806119.1806153 FGFR3_3_4.chr4.1806119.1806153_tile_1 Homo sapiens hg19 chr4 1806119 1806153 - GCTCAGAACCTGGTATCTACTTTCTGT 0 TAGCTGAGGATGCCTGCATACACACTG 0 - ILLUMINA NA 188 TRUE +FGFR3_5_7 FGFR3_5_7.chr4.1807862.1807890 FGFR3_5_7.chr4.1807862.1807890_tile_1 Homo sapiens hg19 chr4 1807862 1807890 - AAACAAGGCCTCAGGCGCCATCCACT 0 GCCAGCCCGAAGTCTGCGATCT 0 - ILLUMINA NA 191 TRUE +FGFR3_8 FGFR3_8.chr4.1808331.1808331 FGFR3_8.chr4.1808331.1808331_tile_1 Homo sapiens hg19 chr4 1808331 1808331 - CCGGAGGGACCCCCACCCCTGA 0 CCCCCAGCGTGAAGATCTCCCA 0 - ILLUMINA NA 171 TRUE +FGFR3_9 FGFR3_9.chr4.1808949.1808949 FGFR3_9.chr4.1808949.1808949_tile_1 Homo sapiens hg19 chr4 1808949 1808949 - AAGCTCTGTGTAGCTGTCTCTCCATCT 0 TCGTGGGCAAACACGGAGTCGTC 0 - ILLUMINA NA 186 TRUE +PDGFRA1_4 PDGFRA1_4.chr4.55141013.55141049 PDGFRA1_4.chr4.55141013.55141049_tile_1 Homo sapiens hg19 chr4 55141013 55141049 - TACCCCATGGAACTTACCAAGCACTAG 0 CTATAAATGACCAGGACAGGTAACTGG 0 - ILLUMINA NA 178 TRUE +PDGFRA5 PDGFRA5.chr4.55144146.55144146 PDGFRA5.chr4.55144146.55144146_tile_1 Homo sapiens hg19 chr4 55144146 55144146 - GTCAGCTCCATTCAAGGGACTTCTATT 0 TACAATGTTCAAATGTGGCCCCAGGT 0 - ILLUMINA NA 188 TRUE +PDGFRA6 PDGFRA6.chr4.55144547.55144547 PDGFRA6.chr4.55144547.55144547_tile_1 Homo sapiens hg19 chr4 55144547 55144547 - AACATCTCTCTTTGCACCCACCTCCGT 0 ATGATGTAAATGGGGCCTATGGGGAC 0 - ILLUMINA NA 186 TRUE +PDGFRA7_23 PDGFRA7_23.chr4.55152040.55152109 PDGFRA7_23.chr4.55152040.55152109_tile_1 Homo sapiens hg19 chr4 55152040 55152109 - AGAGATTAAAGTGAAGGAGGATGAGCC 0 TTGCGAGCAGCCAGATCACGGTGGA 0 - ILLUMINA NA 174 TRUE +KIT1 KIT1.chr4.55561764.55561764 KIT1.chr4.55561764.55561764_tile_1 Homo sapiens hg19 chr4 55561764 55561764 - GTGTTTGTTGGTGCACGTGTATTTGC 0 CCCACGCGGACTATTAAGTCTGATTTT 0 - ILLUMINA NA 179 TRUE +KIT2 KIT2.chr4.55592185.55592186 KIT2.chr4.55592185.55592186_tile_1 Homo sapiens hg19 chr4 55592185 55592186 - CAGTATGGTGTGATGCATGTATTACCA 0 CAGAAGTCTTGCCCACATCGTTGTAA 0 - ILLUMINA NA 188 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_1 Homo sapiens hg19 chr4 55593464 55593689 - GAGAGAACAAATAAATGGTTACCTGTAAA 0 GTGGAATCACAAACTTTGGCAGGA 0 - ILLUMINA NA 172 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_2 Homo sapiens hg19 chr4 55593464 55593689 + CGTAGCTGGCATGATGTGCATTATTG 0 ACCCATGTATGAAGTACAGTGGAAGG 0 + ILLUMINA NA 175 TRUE +KIT3_19 KIT3_19.chr4.55593464.55593689 KIT3_19.chr4.55593464.55593689_tile_3 Homo sapiens hg19 chr4 55593464 55593689 - GTGACATGGAAAGCCCCTGTTTCATA 0 TCTGTGGGGAGAAAGGGAAAAATAGAT 0 - ILLUMINA NA 185 TRUE +KIT20_21 KIT20_21.chr4.55594221.55594258 KIT20_21.chr4.55594221.55594258_tile_1 Homo sapiens hg19 chr4 55594221 55594258 - GCAGTTTATAATCTAGCATTGCCAAAAT 0 AGTTCAGACATGAGGGCTTCCCGTTCT 0 - ILLUMINA NA 189 TRUE +KIT22 KIT22.chr4.55595519.55595519 KIT22.chr4.55595519.55595519_tile_1 Homo sapiens hg19 chr4 55595519 55595519 - ACTATTTATGTAAATCAGTCTTACCAGGA 0 TAATGACCAGGGTGGGCCCTAAAAGC 0 - ILLUMINA NA 184 TRUE +KIT23 KIT23.chr4.55597495.55597497 KIT23.chr4.55597495.55597497_tile_1 Homo sapiens hg19 chr4 55597495 55597497 - CCACATTAGCATGATATACATACTCTCT 0 CTGGGAGAGATGAAACAAGTCATGACT 0 - ILLUMINA NA 187 TRUE +KIT24_28 KIT24_28.chr4.55599320.55599348 KIT24_28.chr4.55599320.55599348_tile_1 Homo sapiens hg19 chr4 55599320 55599348 - TGTGTGATATCCCTAGACAGGATTTAC 0 GGCTAGACCAAAATCACAAATCTTTGT 0 - ILLUMINA NA 184 TRUE +KIT29 KIT29.chr4.55602694.55602694 KIT29.chr4.55602694.55602694_tile_1 Homo sapiens hg19 chr4 55602694 55602694 - GAAGCAGGACACCAATGAAACTTCAAG 0 TGCCATCCACTTCACAGGTAGTCGA 0 - ILLUMINA NA 186 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_1 Homo sapiens hg19 chr4 55946114 55946257 - ATTCTCCAGCCTGACTCGGGGACCACACTG 0 CATTTGATTTTCATTTCGACAACAGAAAAA 0 - ILLUMINA NA 173 TRUE +KDR1 KDR1.chr4.55946114.55946257 KDR1.chr4.55946114.55946257_tile_2 Homo sapiens hg19 chr4 55946114 55946257 + ATGCTTCCTTTTAAACAGGAGGAGAGC 0 GGACTGGTAGCCGCTTGTCTGGTTTGA 0 + ILLUMINA NA 188 TRUE +KDR3 KDR3.chr4.55953807.55953807 KDR3.chr4.55953807.55953807_tile_1 Homo sapiens hg19 chr4 55953807 55953807 - CTGAAGCCATAACAACAGTCTTCTGTG 0 ATTCCATTATGACAACACAGCAGGAAT 0 - ILLUMINA NA 190 TRUE +KDR4 KDR4.chr4.55955111.55955127 KDR4.chr4.55955111.55955127_tile_1 Homo sapiens hg19 chr4 55955111 55955127 - TCCTTATTTAGCATCTCACCTCGTCAG 0 AGCCCAGTCAGAGACCCACGTTTT 0 - ILLUMINA NA 174 TRUE +KDR6 KDR6.chr4.55960989.55961023 KDR6.chr4.55960989.55961023_tile_1 Homo sapiens hg19 chr4 55960989 55961023 - TTTATAGACCAAAGGGGCACGATTCCG 0 TGTAGAAGAAGAGGAAGGTACTGGCTA 0 - ILLUMINA NA 172 TRUE +KDR8 KDR8.chr4.55962507.55962507 KDR8.chr4.55962507.55962507_tile_1 Homo sapiens hg19 chr4 55962507 55962507 - GGAAATGCATGTGGTCTGTAAACTAGG 0 AACACACAGTGAGCATCGAGCTCTCA 0 - ILLUMINA NA 178 TRUE +KDR9 KDR9.chr4.55972964.55972964 KDR9.chr4.55972964.55972964_tile_1 Homo sapiens hg19 chr4 55972964 55972964 - TACCATGGTAGGCTGCGTTGGAAGTTA 0 GACAAACCCATACCCTTGTGAAGAATG 0 - ILLUMINA NA 172 TRUE +KDR10 KDR10.chr4.55979623.55979623 KDR10.chr4.55979623.55979623_tile_1 Homo sapiens hg19 chr4 55979623 55979623 - CTGGTGTCCCTGTTTTTAGCATTAAAT 0 ACCTAAAAACCCAGTCTGGGAGTGAG 0 - ILLUMINA NA 182 TRUE +KDR11 KDR11.chr4.55980348.55980348 KDR11.chr4.55980348.55980348_tile_1 Homo sapiens hg19 chr4 55980348 55980348 - TCTGTGCAAAGTTATAGGCTTATTTGC 0 AGAACTGAACTAAATGTGGGGATTGAC 0 - ILLUMINA NA 178 TRUE +FBXW7_1 FBXW7_1.chr4.153245446.153245446 FBXW7_1.chr4.153245446.153245446_tile_1 Homo sapiens hg19 chr4 153245446 153245446 - CAGTAATTGATAGGAAGAGTATCCATACT 0 AACAAGTGGAATGGAACTCAAAGACAA 0 - ILLUMINA NA 190 TRUE +FBXW7_2 FBXW7_2.chr4.153247288.153247366 FBXW7_2.chr4.153247288.153247366_tile_1 Homo sapiens hg19 chr4 153247288 153247366 - GTTTTGTTTTGTTTTTCTGTTTCTCCCT 0 TATGATGGCAGGAGGGTTGTTAGTGGAGCA 0 - ILLUMINA NA 171 TRUE +FBXW7_5 FBXW7_5.chr4.153249384.153249384 FBXW7_5.chr4.153249384.153249384_tile_1 Homo sapiens hg19 chr4 153249384 153249384 - CATACAGGTGGAGTATGGTCATCACAA 0 AAAAGGTAAGGGAAAATCTTGTCATGG 0 - ILLUMINA NA 184 TRUE +FBXW7_7 FBXW7_7.chr4.153250883.153250883 FBXW7_7.chr4.153250883.153250883_tile_1 Homo sapiens hg19 chr4 153250883 153250883 - CTGTTCCTGTTTATGCCTTCATTTTTC 0 AGTTAGTGGTTCTGATGACAACACTT 0 - ILLUMINA NA 180 TRUE +FBXW7_8 FBXW7_8.chr4.153258983.153258983 FBXW7_8.chr4.153258983.153258983_tile_1 Homo sapiens hg19 chr4 153258983 153258983 - CTGTAATTTGGGACATCTGTTAAAACAATA 0 GACTTCATTTCATTGCTCCCTAAAGAGG 0 - ILLUMINA NA 191 TRUE +APC1 APC1.chr5.112173917.112173917 APC1.chr5.112173917.112173917_tile_1 Homo sapiens hg19 chr5 112173917 112173917 - GCAGAGCTTCTTCTAAGTGCATTTCTC 0 TGAAGAAGTTCCTGGATTTTCTGTTGC 0 - ILLUMINA NA 186 TRUE +APC2 APC2.chr5.112174631.112174631 APC2.chr5.112174631.112174631_tile_1 Homo sapiens hg19 chr5 112174631 112174631 - AATTTGTTGGTCTCTCTTCTTCTTCAT 0 TTTGTTTCTGAACCATTGGCTCCCCGT 0 - ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_1 Homo sapiens hg19 chr5 112175162 112175958 + CTTGCAAAGTTTCTTCTATTAACCAAGA 0 TTCTGCTAATACCCTGCAAATAGCAGA 0 + ILLUMINA NA 176 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_2 Homo sapiens hg19 chr5 112175162 112175958 - TGCTGGATTTGGTTCTAGGGTGCT 0 CCTATTTCATCTTCAGCTGATGACAAA 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_3 Homo sapiens hg19 chr5 112175162 112175958 + GAAAAGATTGGAACTAGGTCAGCTGAAG 0 AGCGAAATCTCCCTCCAAAAGTGGT 0 + ILLUMINA NA 172 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_4 Homo sapiens hg19 chr5 112175162 112175958 - CTATCAAGTGAACTGACAGAAGTACATC 0 CCTGGCTGATTCTGAAGATAAACTAGAACC 0 - ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_5 Homo sapiens hg19 chr5 112175162 112175958 + CACCCAAAAGTCCACCTGAACACTAT 0 ATTATAAGCCCCAGTGATCTTCCAGAT 0 + ILLUMINA NA 174 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_6 Homo sapiens hg19 chr5 112175162 112175958 - CTCTCTCTTTTCAGCAGTAGGTGCTT 0 CACTTACCATTCCACTGCATGGTTCA 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_7 Homo sapiens hg19 chr5 112175162 112175958 + CAAACCAAGCGAGAAGTACCTAAAAAT 0 AAAGTACTCCAGATGGATTTTCTTGTTC 0 + ILLUMINA NA 171 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_8 Homo sapiens hg19 chr5 112175162 112175958 - CTCTGATTCTGTTTCATTCCCATTGTCATT 0 GTGGCAAAATGTAATAAAGTATCAGCATCT 0 - ILLUMINA NA 173 TRUE +APC3_42 APC3_42.chr5.112175162.112175958 APC3_42.chr5.112175162.112175958_tile_9 Homo sapiens hg19 chr5 112175162 112175958 + ATTAAGAATAATGCCTCCAGTTCAGGA 0 AGAAGAATGTATTATTTCTGCCATGCC 0 + ILLUMINA NA 190 TRUE +CSF1R1_3 CSF1R1_3.chr5.149433644.149433646 CSF1R1_3.chr5.149433644.149433646_tile_1 Homo sapiens hg19 chr5 149433644 149433646 - TCCCACCCTCAGGACTATACCAATCT 0 AGTTCTGCTGAGGAGTTGACGACAGGG 0 - ILLUMINA NA 185 TRUE +CSF1R4 CSF1R4.chr5.149453044.149453044 CSF1R4.chr5.149453044.149453044_tile_1 Homo sapiens hg19 chr5 149453044 149453044 - TCTTGGGTGGTGGGGACTATGTACCT 0 AACTTGAGCTCTGAGCAGAACCTCATC 0 - ILLUMINA NA 175 TRUE +NPM1 NPM1.chr5.170837547.170837548 NPM1.chr5.170837547.170837548_tile_1 Homo sapiens hg19 chr5 170837547 170837548 - GGTAGGGAAAGTTCTCACTCTGCATTA 0 AAAAAGAAATGTGGTTAAGGAACCAC 0 - ILLUMINA NA 186 TRUE +EGFR1 EGFR1.chr7.55211080.55211080 EGFR1.chr7.55211080.55211080_tile_1 Homo sapiens hg19 chr7 55211080 55211080 - CATCGGAACTGCTGTCTGCATTTATGA 0 GATGATCTGCAGGTTTTCCAAAGGAAT 0 - ILLUMINA NA 188 TRUE +EGFR2 EGFR2.chr7.55221822.55221822 EGFR2.chr7.55221822.55221822_tile_1 Homo sapiens hg19 chr7 55221822 55221822 - AAGCAAGGCAAACACATCCACCCAAAG 0 AAAGCTGTATTTGCCCTCGGGGTTCA 0 - ILLUMINA NA 174 TRUE +EGFR3 EGFR3.chr7.55233043.55233043 EGFR3.chr7.55233043.55233043_tile_1 Homo sapiens hg19 chr7 55233043 55233043 - AACTTGGGAGACATTTTTGATCTCTGA 0 TGCCGGGCAGGTCTTGACGCAGT 0 - ILLUMINA NA 186 TRUE +EGFR4 EGFR4.chr7.55241677.55241708 EGFR4.chr7.55241677.55241708_tile_1 Homo sapiens hg19 chr7 55241677 55241708 - GGAAATATACAGCTTGCAAGGACTCTG 0 TCAAGATCCTCAAGAGAGCTTGGTTG 0 - ILLUMINA NA 180 TRUE +EGFR9 EGFR9.chr7.55242418.55242511 EGFR9.chr7.55242418.55242511_tile_1 Homo sapiens hg19 chr7 55242418 55242511 - ATGAGAAAAGGTGGGCCTGAGGTTCAG 0 CCTATGACAGAGAGAGAAGGAAGACGTT 0 - ILLUMINA NA 190 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_1 Homo sapiens hg19 chr7 55249005 55249131 - AGGTGAGGCAGATGCCCAGCAGGCGG 0 CGCATGAATGCGATCTTGAGTTTCAA 0 - ILLUMINA NA 175 TRUE +EGFR44 EGFR44.chr7.55249005.55249131 EGFR44.chr7.55249005.55249131_tile_2 Homo sapiens hg19 chr7 55249005 55249131 + CAGCGTGGACAACCCCCACGTGT 0 GTGTGTGCAGATCGCAAAGGTAATCA 0 + ILLUMINA NA 177 TRUE +EGFR54 EGFR54.chr7.55259514.55259524 EGFR54.chr7.55259514.55259524_tile_1 Homo sapiens hg19 chr7 55259514 55259524 - CCTCCCCTGCATGTGTTAAACAATACA 0 CCAAAATCTGTGATCTTGACATGCTGC 0 - ILLUMINA NA 178 TRUE +MET1 MET1.chr7.116339642.116339642 MET1.chr7.116339642.116339642_tile_1 Homo sapiens hg19 chr7 116339642 116339642 - CCTTCTCACTGATATCGAATGCAATGG 0 CTTCTATCTGTGGGGAGAATATGCAGT 0 - ILLUMINA NA 180 TRUE +MET2 MET2.chr7.116340262.116340262 MET2.chr7.116340262.116340262_tile_1 Homo sapiens hg19 chr7 116340262 116340262 - GCCCTGGATATTCTTTTTGAGACTGAT 0 GAAGAAGTCGTTGACATATTTGATAGG 0 - ILLUMINA NA 188 TRUE +MET3 MET3.chr7.116411990.116411990 MET3.chr7.116411990.116411990_tile_1 Homo sapiens hg19 chr7 116411990 116411990 - TGCAAAACCAAAAATAAACAACAATGTC 0 TTACACTTCGGGCACTTACAAGCCTA 0 - ILLUMINA NA 171 TRUE +MET4 MET4.chr7.116417463.116417464 MET4.chr7.116417463.116417464_tile_1 Homo sapiens hg19 chr7 116417463 116417464 - CACAAGGGGAAAGTGTAAATCAACGTTT 0 CACAACCAAAATGCCCTGTGCAAAAGA 0 - ILLUMINA NA 191 TRUE +MET6 MET6.chr7.116423413.116423474 MET6.chr7.116423413.116423474_tile_1 Homo sapiens hg19 chr7 116423413 116423474 - GAGGAGAAACTCAGAGATAACCAATAC 0 TGTCTCTGGCAAGACCAAAATCAGCA 0 - ILLUMINA NA 172 TRUE +SMO1 SMO1.chr7.128845101.128845101 SMO1.chr7.128845101.128845101_tile_1 Homo sapiens hg19 chr7 128845101 128845101 - TGACCAGGGTGAAGAGCGTGCAGAG 0 AAGGGCACTTCGCACTGGCCTGAA 0 - ILLUMINA NA 186 TRUE +SMO2 SMO2.chr7.128846040.128846040 SMO2.chr7.128846040.128846040_tile_1 Homo sapiens hg19 chr7 128846040 128846040 - ATTGCCACAGTGAGGACAAAGGGGAGT 0 GTACACGATGACAAAGATGATGACGCA 0 - ILLUMINA NA 186 TRUE +SMO3 SMO3.chr7.128846374.128846374 SMO3.chr7.128846374.128846374_tile_1 Homo sapiens hg19 chr7 128846374 128846374 - TAGCTGGGGTTTCAGCATGGGGGCAGC 0 AAGCCCGCACGGTATCGGTAGTTCT 0 - ILLUMINA NA 190 TRUE +SMO4 SMO4.chr7.128850341.128850341 SMO4.chr7.128850341.128850341_tile_1 Homo sapiens hg19 chr7 128850341 128850341 - AACCACTGACCAAGGCTGTGCTAGAGG 0 TCATGGCGATGCCAGTTCCAAACA 0 - ILLUMINA NA 190 TRUE +SMO5 SMO5.chr7.128851593.128851593 SMO5.chr7.128851593.128851593_tile_1 Homo sapiens hg19 chr7 128851593 128851593 - TTCAGATCCTCTGGGGCCTTTCCTTC 0 AGAAATATCCTGGGGCAGTATGGCTCC 0 - ILLUMINA NA 173 TRUE +BRAF1 BRAF1.chr7.140453121.140453193 BRAF1.chr7.140453121.140453193_tile_1 Homo sapiens hg19 chr7 140453121 140453193 - ACCTAAACTCTTCATAATGCTTGCTCT 0 GGTCCCATCAGTTTGAACAGTTGTCT 0 - ILLUMINA NA 176 TRUE +BRAF28 BRAF28.chr7.140481397.140481478 BRAF28.chr7.140481397.140481478_tile_1 Homo sapiens hg19 chr7 140481397 140481478 - GGTTTTCTTTTTCTGTTTGGCTTGACT 0 CTACAAGGGAAAGTGGCATGGTAAGTA 0 - ILLUMINA NA 178 TRUE +FGFR1_1 FGFR1_1.chr8.38282209.38282209 FGFR1_1.chr8.38282209.38282209_tile_1 Homo sapiens hg19 chr8 38282209 38282209 - TTTTGAGAGGCTTGGGCTCAGCAGAA 0 TCACCGGCCCATCCTGCAAGCAGGG 0 - ILLUMINA NA 179 TRUE +FGFR1_2 FGFR1_2.chr8.38285938.38285938 FGFR1_2.chr8.38285938.38285938_tile_1 Homo sapiens hg19 chr8 38285938 38285938 - AAGAGATCATCACTAAGGGAGCAGTGG 0 GGATGATGATGATGATGATGACTCCTC 0 - ILLUMINA NA 184 TRUE +JAK2_1 JAK2_1.chr9.5073769.5073770 JAK2_1.chr9.5073769.5073770_tile_1 Homo sapiens hg19 chr9 5073769 5073770 - TTCAGTTTCAAAAATACTTAACTCCTGTT 0 CTCCATAATTTAAAACCAAATGCTTGTG 0 - ILLUMINA NA 188 TRUE +CDKN2A1 CDKN2A1.chr9.21971153.21971187 CDKN2A1.chr9.21971153.21971187_tile_1 Homo sapiens hg19 chr9 21971153 21971187 - TTGTGTGGGGGTCTGCTTGGCGGTGA 0 AACTGCGCCGACCCCGCCACTCTCA 0 - ILLUMINA NA 187 TRUE +ABL1_1 ABL1_1.chr9.133738330.133738364 ABL1_1.chr9.133738330.133738364_tile_1 Homo sapiens hg19 chr9 133738330 133738364 - ATGCATCGCCTAATGCCAGCAGACGC 0 TGATGTCCGTGCGTTCCATCTCCCAC 0 - ILLUMINA NA 191 TRUE +ABL1_9 ABL1_9.chr9.133747520.133747520 ABL1_9.chr9.133747520.133747520_tile_1 Homo sapiens hg19 chr9 133747520 133747520 - AGCGCCTGTGTCACCCTGGGGGT 0 AAAACGAAGGTGAAATTATTTCAGGAA 0 - ILLUMINA NA 190 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_1 Homo sapiens hg19 chr9 133748283 133748414 + AGAATCCTTCAGAAGGCTTTTTCTTTAGAC 0 AACCTCCTGGACTACCTGAGGGAGT 0 + ILLUMINA NA 172 TRUE +ABL1_10 ABL1_10.chr9.133748283.133748414 ABL1_10.chr9.133748283.133748414_tile_2 Homo sapiens hg19 chr9 133748283 133748414 - TCCATGGCGCAGGCTGCCTGGCC 0 CCGTAGGTCATGAACTCAGTGATGA 0 - ILLUMINA NA 182 TRUE +ABL1_16 ABL1_16.chr9.133750356.133750356 ABL1_16.chr9.133750356.133750356_tile_1 Homo sapiens hg19 chr9 133750356 133750356 - GGGAAGAGCAAGAAAGAGGCAGAAAAA 0 TGTGTAGGTGTCCCCTGTCATCAA 0 - ILLUMINA NA 190 TRUE +NOTCH1_1 NOTCH1_1.chr9.139397768.139397768 NOTCH1_1.chr9.139397768.139397768_tile_1 Homo sapiens hg19 chr9 139397768 139397768 - AGACCTGGCTTCCCACCACCCCAGGCT 0 AGATTGACAACCGGCAGTGTGTGCAG 0 - ILLUMINA NA 190 TRUE +NOTCH1_2 NOTCH1_2.chr9.139399344.139399422 NOTCH1_2.chr9.139399344.139399422_tile_1 Homo sapiens hg19 chr9 139399344 139399422 - AGTGCGAGTGGGACGGGCTGGACTGT 0 ACACCAACGTGGTCTTCAAGCGTGAC 0 - ILLUMINA NA 171 TRUE +RET1 RET1.chr10.43609078.43609104 RET1.chr10.43609078.43609104_tile_1 Homo sapiens hg19 chr10 43609078 43609104 - ACTCGCCTCCCAGCAATTTCCTCCC 0 TTGCAGGTGCCATAGCCAGCTTTAAT 0 - ILLUMINA NA 180 TRUE +RET2_9 RET2_9.chr10.43609940.43609950 RET2_9.chr10.43609940.43609950_tile_1 Homo sapiens hg19 chr10 43609940 43609950 + AAGCCTCACACCACCCCCACCCACAGAT 0 CCCATCTCCTCAGCTGAGATGACCTT 0 + ILLUMINA NA 175 TRUE +RET10 RET10.chr10.43613840.43613840 RET10.chr10.43613840.43613840_tile_1 Homo sapiens hg19 chr10 43613840 43613840 - AGAACAGGGCTGTATGGAGCCCCCAGC 0 GGGAGGCGTTCTCTGAAATGCAG 0 - ILLUMINA NA 190 TRUE +RET11_12 RET11_12.chr10.43615567.43615569 RET11_12.chr10.43615567.43615569_tile_1 Homo sapiens hg19 chr10 43615567 43615569 - ATGGTGCACCTGGGATCCCTGGGAG 0 ATGTTTCTGGCTGCCAAGTCCCGATGAA 0 - ILLUMINA NA 172 TRUE +RET13 RET13.chr10.43617416.43617416 RET13.chr10.43617416.43617416_tile_1 Homo sapiens hg19 chr10 43617416 43617416 - AATTCCCTGGCCAAGCTGCACAGACGG 0 CCATTTAACTGGAATCCGACCCTAAAG 0 - ILLUMINA NA 178 TRUE +PTEN1 PTEN1.chr10.89624242.89624244 PTEN1.chr10.89624242.89624244_tile_1 Homo sapiens hg19 chr10 89624242 89624244 - TACGGACATTTTCGCATCCGTCTACTC 0 ATGATGGCTGTCATGTCTGGGAGCCTG 0 - ILLUMINA NA 176 TRUE +PTEN3 PTEN3.chr10.89685307.89685307 PTEN3.chr10.89685307.89685307_tile_1 Homo sapiens hg19 chr10 89685307 89685307 - TGGACTTCTTGACTTAATCGGTTTAGG 0 CTTGTAATGGTTTTTATGCTTTGAATCCA 0 - ILLUMINA NA 186 TRUE +PTEN4 PTEN4.chr10.89711893.89711900 PTEN4.chr10.89711893.89711900_tile_1 Homo sapiens hg19 chr10 89711893 89711900 - GGATGAGAATTTCAAGCACTTACTGCA 0 TGGGAATAGTTACTCCCTGGTGGACA 0 - ILLUMINA NA 176 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_1 Homo sapiens hg19 chr10 89717615 89717772 - GGGTCCTGAATTGGAGGAATATATCTTCAC 0 ACACGAAATATGGATTCTGTATCTGC 0 - ILLUMINA NA 181 TRUE +PTEN7 PTEN7.chr10.89717615.89717772 PTEN7.chr10.89717615.89717772_tile_2 Homo sapiens hg19 chr10 89717615 89717772 + CAGTTTGTGGTCTGCCAGCTAAA 0 AAAGGTTTGTACTTTACTTTCATTGGGAG 0 + ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_1 Homo sapiens hg19 chr10 89720716 89720852 - AATTTGGAGAAAAGTATCGGTTGGCTT 0 AGGTTTCCTCTGGTCCTGGTATGAA 0 - ILLUMINA NA 188 TRUE +PTEN13 PTEN13.chr10.89720716.89720852 PTEN13.chr10.89720716.89720852_tile_2 Homo sapiens hg19 chr10 89720716 89720852 + AAAATGATCTTGACAAAGCAAATAAAGAC 0 CTTGCTTGACAAGTTTTTAACTTATGTATT 0 + ILLUMINA NA 179 TRUE +FGFR2_1 FGFR2_1.chr10.123258034.123258034 FGFR2_1.chr10.123258034.123258034_tile_1 Homo sapiens hg19 chr10 123258034 123258034 - CTAACAGTAGCTGCCCATGAGTTAGAG 0 TTCTTGGAGCCTGCACACAGGATGGTG 0 - ILLUMINA NA 180 TRUE +FGFR2_2 FGFR2_2.chr10.123274774.123274803 FGFR2_2.chr10.123274774.123274803_tile_1 Homo sapiens hg19 chr10 123274774 123274803 - GCCTTTTGGTTCCTTTGGTTGTGCTAT 0 CATAGGGGTCTTCTTAATCGCCTGTAT 0 - ILLUMINA NA 186 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_1 Homo sapiens hg19 chr10 123279503 123279677 - CACGTGGAAAAGAACGGCAGTAAATAC 0 GGAGTTGAGAGAGGATGATTCTCTTTT 0 - ILLUMINA NA 172 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_2 Homo sapiens hg19 chr10 123279503 123279677 + TTTAGATTCAGAAAGTCCTCACCTTGAG 0 CTCCTCCGACCACTGTGGAGGCATTT 0 + ILLUMINA NA 171 TRUE +FGFR2_5 FGFR2_5.chr10.123279503.123279677 FGFR2_5.chr10.123279503.123279677_tile_3 Homo sapiens hg19 chr10 123279503 123279677 - ACTGACAGCCCTCTGGACAACACAGCT 0 CGTAGAGTTTGTCTGCAAGGTTTACAG 0 - ILLUMINA NA 184 TRUE +HRAS1 HRAS1.chr11.533873.533875 HRAS1.chr11.533873.533875_tile_1 Homo sapiens hg19 chr11 533873 533875 - TACCAGGGAGAGGCTGGCTGTGTGAAC 0 AGTACAGCGCCATGCGGGACCAGTAC 0 - ILLUMINA NA 180 TRUE +HRAS6 HRAS6.chr11.534285.534289 HRAS6.chr11.534285.534289_tile_1 Homo sapiens hg19 chr11 534285 534289 - CTGCCCTGTGGGGCCTGGGGCTGG 0 AAGAGTGCGCTGACCATCCAGCTGATC 0 - ILLUMINA NA 185 TRUE +ATM1 ATM1.chr11.108117847.108117848 ATM1.chr11.108117847.108117848_tile_1 Homo sapiens hg19 chr11 108117847 108117848 - GAAAGGAATAGTTGCATGTACAGAGTC 0 GATATCTGCCATCAATTCAATCAAATTTT 0 - ILLUMINA NA 174 TRUE +ATM2 ATM2.chr11.108119823.108119823 ATM2.chr11.108119823.108119823_tile_1 Homo sapiens hg19 chr11 108119823 108119823 - TTGCTAGTAATAGGTTTGGGGGTAGAC 0 GATCAAAATCATTCTGTGACTTCTGAA 0 - ILLUMINA NA 172 TRUE +ATM3 ATM3.chr11.108123551.108123551 ATM3.chr11.108123551.108123551_tile_1 Homo sapiens hg19 chr11 108123551 108123551 - AAGCTATAGCTTAAAATGATAAAGAGCAT 0 ACAAAGAAAAACAAAAAGCTTCACTTAGA 0 - ILLUMINA NA 172 TRUE +ATM4 ATM4.chr11.108137973.108138003 ATM4.chr11.108137973.108138003_tile_1 Homo sapiens hg19 chr11 108137973 108138003 - ACTGCCAAATCAATATAAAGAAGTAAAAGA 0 GATTTCCATTAGTATCATCTTCCATTGAT 0 - ILLUMINA NA 189 TRUE +ATM6 ATM6.chr11.108155132.108155132 ATM6.chr11.108155132.108155132_tile_1 Homo sapiens hg19 chr11 108155132 108155132 - TCGAATAAATAGCCTTAAAACTTAAAGGTT 0 ATCCCACTGTCTCTGGTACCCTCATAG 0 - ILLUMINA NA 179 TRUE +ATM7 ATM7.chr11.108170476.108170479 ATM7.chr11.108170476.108170479_tile_1 Homo sapiens hg19 chr11 108170476 108170479 - ACTCACCAATCTTCTACCAGTGTGTTA 0 ACTTCTCCCAAGCAGCTTCCAACAGCC 0 - ILLUMINA NA 178 TRUE +ATM9 ATM9.chr11.108172421.108172421 ATM9.chr11.108172421.108172421_tile_1 Homo sapiens hg19 chr11 108172421 108172421 - ACAGAACTGTTTTAGATATGCTGGGTA 0 AATGTTTTTCAAACAGGTAACAGCTGC 0 - ILLUMINA NA 182 TRUE +ATM10 ATM10.chr11.108173640.108173640 ATM10.chr11.108173640.108173640_tile_1 Homo sapiens hg19 chr11 108173640 108173640 - CAGGTCATAAACAAGGAATTATATCAGACT 0 ATATCATCCAGGCCTTCAAAAGGG 0 - ILLUMINA NA 191 TRUE +ATM11 ATM11.chr11.108180945.108180945 ATM11.chr11.108180945.108180945_tile_1 Homo sapiens hg19 chr11 108180945 108180945 - CCCTTATTGAGACAATGCCAACATTAA 0 CTAGATAATTTAAATCCAGCCAGAAAGC 0 - ILLUMINA NA 188 TRUE +ATM12 ATM12.chr11.108200958.108200961 ATM12.chr11.108200958.108200961_tile_1 Homo sapiens hg19 chr11 108200958 108200961 - CAAAGTCGGAATACCCACATATCATGT 0 CCTTTACTGTGTATCTTGCATAGAATAAT 0 - ILLUMINA NA 172 TRUE +ATM14 ATM14.chr11.108204681.108204681 ATM14.chr11.108204681.108204681_tile_1 Homo sapiens hg19 chr11 108204681 108204681 - TAGGTTGAAACATATGAAATTTGCCAA 0 GGGACAACAACATCTTCTAAATTCTTAAG 0 - ILLUMINA NA 174 TRUE +ATM15 ATM15.chr11.108205769.108205769 ATM15.chr11.108205769.108205769_tile_1 Homo sapiens hg19 chr11 108205769 108205769 - GACAAAATCCCAAATAAAGCAGAAAGAA 0 CCTGCTAAGCGAAATTCTGCTTTAAATG 0 - ILLUMINA NA 191 TRUE +ATM16 ATM16.chr11.108206594.108206594 ATM16.chr11.108206594.108206594_tile_1 Homo sapiens hg19 chr11 108206594 108206594 - CACCCAACCAAATGGCATCTTTTATAT 0 TTGTCTCAGGTCATCACGGCCCTTCAG 0 - ILLUMINA NA 186 TRUE +ATM17 ATM17.chr11.108218089.108218089 ATM17.chr11.108218089.108218089_tile_1 Homo sapiens hg19 chr11 108218089 108218089 - CTAGGACAACTGTTTATGCTGAAAACA 0 TCTATATGTACAAGTTCTGCTGACTGC 0 - ILLUMINA NA 188 TRUE +ATM18 ATM18.chr11.108225590.108225590 ATM18.chr11.108225590.108225590_tile_1 Homo sapiens hg19 chr11 108225590 108225590 - GCTAAGTGCACAATCTCCTCCTTTCT 0 AACAGAGTTTCCTGAGAGTTTCTCATC 0 - ILLUMINA NA 191 TRUE +ATM19 ATM19.chr11.108236086.108236203 ATM19.chr11.108236086.108236203_tile_1 Homo sapiens hg19 chr11 108236086 108236203 - TGAAGATCACACCCAAGCTTTCCATC 0 TCAGCTACTTTGTTGAAACTCTGGTCA 0 - ILLUMINA NA 185 TRUE +KRAS1 KRAS1.chr12.25378562.25378562 KRAS1.chr12.25378562.25378562_tile_1 Homo sapiens hg19 chr12 25378562 25378562 - TCTTTCCCAGAGAACAAATTAAAAGAGT 0 AGACAAGACAGGTAAGTAACACTGAAA 0 - ILLUMINA NA 187 TRUE +KRAS2 KRAS2.chr12.25380275.25380283 KRAS2.chr12.25380275.25380283_tile_1 Homo sapiens hg19 chr12 25380275 25380283 - TTGTTGTTGAGTTGTATATAACACCTTTT 0 AGTACAGTGCAATGAGGGACCAGTAC 0 - ILLUMINA NA 184 TRUE +KRAS7 KRAS7.chr12.25398255.25398285 KRAS7.chr12.25398255.25398285_tile_1 Homo sapiens hg19 chr12 25398255 25398285 - GGTACTGGTGGAGTATTTGATAGTGTAT 0 GCTAATTCAGAATCATTTTGTGGACGAAT 0 - ILLUMINA NA 191 TRUE +PTPN11_1 PTPN11_1.chr12.112888163.112888211 PTPN11_1.chr12.112888163.112888211_tile_1 Homo sapiens hg19 chr12 112888163 112888211 - TACTGACCTTTCAGAGGTAGGATCTGC 0 GTGTTCTGAATCTTGATGTGGGTGAC 0 - ILLUMINA NA 190 TRUE +PTPN11_10 PTPN11_10.chr12.112926884.112926888 PTPN11_10.chr12.112926884.112926888_tile_1 Homo sapiens hg19 chr12 112926884 112926888 - CAAGAGGCCTAGCAAGAGAATGAGAAT 0 TCTGAGACCGCACCATCTGGATGGTT 0 - ILLUMINA NA 178 TRUE +HNF1A_1 HNF1A_1.chr12.121431413.121431414 HNF1A_1.chr12.121431413.121431414_tile_1 Homo sapiens hg19 chr12 121431413 121431414 - TTGCCGCAGCCCAGACCAAACCAGCA 0 TTGAAACGGTTCCTCCGCCCCTTCTT 0 - ILLUMINA NA 175 TRUE +HNF1A_3 HNF1A_3.chr12.121432070.121432070 HNF1A_3.chr12.121432070.121432070_tile_1 Homo sapiens hg19 chr12 121432070 121432070 - ACATACCACTTACCGTGGACCTTACT 0 CGGTTGGCAAACCAGTTGTAGACA 0 - ILLUMINA NA 181 TRUE +FLT3_1 FLT3_1.chr13.28592620.28592653 FLT3_1.chr13.28592620.28592653_tile_1 Homo sapiens hg19 chr13 28592620 28592653 - CACATCACAGTAAATAACACTCTGGTG 0 TTGTCAGGGGCAATGTGAGGCTGCTATT 0 - ILLUMINA NA 178 TRUE +FLT3_13 FLT3_13.chr13.28602329.28602329 FLT3_13.chr13.28602329.28602329_tile_1 Homo sapiens hg19 chr13 28602329 28602329 - ACTTGAGTTTTACATTTTTAATGCTCCT 0 TGTCAGGTAACCCACTTCCACGAAAA 0 - ILLUMINA NA 171 TRUE +FLT3_14 FLT3_14.chr13.28608244.28608341 FLT3_14.chr13.28608244.28608341_tile_1 Homo sapiens hg19 chr13 28608244 28608341 - CTATCTGCAGAACTGCCTATTCCTAAC 0 TTCCAAGAGAAAATTTAGAGTTTGGTAAG 0 - ILLUMINA NA 190 TRUE +FLT3_22 FLT3_22.chr13.28610138.28610138 FLT3_22.chr13.28610138.28610138_tile_1 Homo sapiens hg19 chr13 28610138 28610138 + CCAGGTCCAAGATGGTAATGGGTAT 0 ATACCAATACTTTGTGAAGCCAAGGTGG 0 + ILLUMINA NA 171 TRUE +RB1_1 RB1_1.chr13.48919244.48919244 RB1_1.chr13.48919244.48919244_tile_1 Homo sapiens hg19 chr13 48919244 48919244 - CCTTTCCAATTTGCTGAAGAGTGCAAA 0 CAGTAACCTTAAAAATTTGTGTTATTTCGT 0 - ILLUMINA NA 182 TRUE +RB1_2 RB1_2.chr13.48923148.48923148 RB1_2.chr13.48923148.48923148_tile_1 Homo sapiens hg19 chr13 48923148 48923148 - GCTAACAGTTAATAAGCCAAGCAGAGA 0 AAATGTGATCCAAGAAACTTTTAGCAC 0 - ILLUMINA NA 178 TRUE +RB1_3 RB1_3.chr13.48942685.48942685 RB1_3.chr13.48942685.48942685_tile_1 Homo sapiens hg19 chr13 48942685 48942685 - ACATAAAGAAACGTGAACAAATCTGAAA 0 GGTGTTCTCTGTGTTTCAAAACTAAATAA 0 - ILLUMINA NA 173 TRUE +RB1_4 RB1_4.chr13.48955538.48955550 RB1_4.chr13.48955538.48955550_tile_1 Homo sapiens hg19 chr13 48955538 48955550 - TTCCCTATATGTTCTTGAGGTAGATGT 0 AATGTTTTATCATTTCTCTTGTCAAGTTG 0 - ILLUMINA NA 182 TRUE +RB1_6 RB1_6.chr13.49027168.49027168 RB1_6.chr13.49027168.49027168_tile_1 Homo sapiens hg19 chr13 49027168 49027168 - TTTGCAGTTTGAATGGTCAACATAACA 0 TAAAGGTGAATCCTATATGAAACATGATG 0 - ILLUMINA NA 178 TRUE +RB1_7 RB1_7.chr13.49033843.49033846 RB1_7.chr13.49033843.49033846_tile_1 Homo sapiens hg19 chr13 49033843 49033846 - GAAGTGCTTGATTTTCTTACTTGGTCC 0 TAGGCTAGCCGATACACTGTGGGAATA 0 - ILLUMINA NA 178 TRUE +RB1_8 RB1_8.chr13.49037877.49037877 RB1_8.chr13.49037877.49037877_tile_1 Homo sapiens hg19 chr13 49037877 49037877 - GGAAAATTACCTACCTCCTGAACAGCA 0 AGTAGTCAGAATTTTATTACATGGTTTTGT 0 - ILLUMINA NA 172 TRUE +RB1_9 RB1_9.chr13.49039164.49039164 RB1_9.chr13.49039164.49039164_tile_1 Homo sapiens hg19 chr13 49039164 49039164 - TGTTTTGGTGGACCCATTACATTAGAT 0 CTTTGATCAAAACACGTTTGAATGTCT 0 - ILLUMINA NA 174 TRUE +AKT1 AKT1.chr14.105246455.105246455 AKT1.chr14.105246455.105246455_tile_1 Homo sapiens hg19 chr14 105246455 105246455 - TCTGACGGGTAGAGTGTGCGTGGCTC 0 GCTCCCCTCAACAACTTCTCTGTG 0 - ILLUMINA NA 173 TRUE +CDH1_1 CDH1_1.chr16.68835649.68835650 CDH1_1.chr16.68835649.68835650_tile_1 Homo sapiens hg19 chr16 68835649 68835650 - GGCGGTGGTGGTGCCCCACTGT 0 CTTTGAATCGGGTGTCGAGGGAAAAA 0 - ILLUMINA NA 171 TRUE +CDH1_2 CDH1_2.chr16.68846137.68846137 CDH1_2.chr16.68846137.68846137_tile_1 Homo sapiens hg19 chr16 68846137 68846137 - ACATTCTCTAGTCTGGAGAGAGTTTTC 0 TTGGTGTCAGTGACTGTGATCACAGCT 0 - ILLUMINA NA 176 TRUE +CDH1_3 CDH1_3.chr16.68847274.68847277 CDH1_3.chr16.68847274.68847277_tile_1 Homo sapiens hg19 chr16 68847274 68847277 - CATCTTGCCAGGTACCATACAAACCTT 0 CACTTTCAGTGTGGTGATTACGACGTT 0 - ILLUMINA NA 178 TRUE +TP53_1 TP53_1.chr17.7574003.7574021 TP53_1.chr17.7574003.7574021_tile_1 Homo sapiens hg19 chr17 7574003 7574021 - ACTAAATGCATGTTGCTTTTGTACCGT 0 AGAGCTGAATGAGGCCTTGGAACTC 0 - ILLUMINA NA 172 TRUE +TP53_3 TP53_3.chr17.7577022.7577129 TP53_3.chr17.7577022.7577129_tile_1 Homo sapiens hg19 chr17 7577022 7577129 - ATCCTGAGTAGTGGTAATCTACTGGGA 0 AGGTAAGCAAGCAGGACAAGAAGCG 0 - ILLUMINA NA 172 TRUE +TP53_17 TP53_17.chr17.7577523.7577574 TP53_17.chr17.7577523.7577574_tile_1 Homo sapiens hg19 chr17 7577523 7577574 - AAAAAGGCCTCCCCTGCTTGCCACAGG 0 ATCATCACACTGGAAGACTCCAGGTCA 0 - ILLUMINA NA 190 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_1 Homo sapiens hg19 chr17 7578190 7578536 - TTTGGATGACAGAAACACTTTTCGACA 0 CCTGCTGCTTATTTGACCTCCCTATAAC 0 - ILLUMINA NA 172 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_2 Homo sapiens hg19 chr17 7578190 7578536 + GACCCCAGTTGCAAACCAGACCTCA 0 TGAGGAATCAGAGGCCTGGGGA 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_3 Homo sapiens hg19 chr17 7578190 7578536 - TTGTGAGGCGCTGCCCCCACCATGAG 0 GCATCTTATCCGAGTGGAAGGAAATTTG 0 - ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_4 Homo sapiens hg19 chr17 7578190 7578536 + CGTCTCTCCAGCCCCAGCTGCTCACCAT 0 CCACAGCTGCACAGGGCAGGTCTT 0 + ILLUMINA NA 171 TRUE +TP53_31_59 TP53_31_59.chr17.7578190.7578536 TP53_31_59.chr17.7578190.7578536_tile_5 Homo sapiens hg19 chr17 7578190 7578536 - GCATGTTTGTTTCTTTGCTGCCGTCT 0 TTGATTCCACACCCCCGCCCGGC 0 - ILLUMINA NA 179 TRUE +TP53_60 TP53_60.chr17.7579358.7579403 TP53_60.chr17.7579358.7579403_tile_1 Homo sapiens hg19 chr17 7579358 7579403 - AGATGAAGCTCCCAGAATGCCAGAGG 0 TTCTTGCATTCTGGGACAGCCAAGTCT 0 - ILLUMINA NA 185 TRUE +TP53_64 TP53_64.chr17.7579882.7579882 TP53_64.chr17.7579882.7579882_tile_1 Homo sapiens hg19 chr17 7579882 7579882 - ATGGTGTTGGGGGAGGGGGTTCCTTCT 0 CCCCTCTGAGTCAGGAAACATTTTCAG 0 - ILLUMINA NA 182 TRUE +ERBB2_1 ERBB2_1.chr17.37880219.37880261 ERBB2_1.chr17.37880219.37880261_tile_1 Homo sapiens hg19 chr17 37880219 37880261 - CATATCTCCCCAAACCCCAATGAAGAG 0 CTTTGATGGCCACTGGAATTTTCACA 0 - ILLUMINA NA 172 TRUE +ERBB2_4 ERBB2_4.chr17.37880993.37881012 ERBB2_4.chr17.37880993.37881012_tile_1 Homo sapiens hg19 chr17 37880993 37881012 - ATACACCAGTTCAGCAGGTCCTGGGAG 0 TATGCTTCCTGGGGACAAGGGTAC 0 - ILLUMINA NA 190 TRUE +ERBB2_13 ERBB2_13.chr17.37881332.37881440 ERBB2_13.chr17.37881332.37881440_tile_1 Homo sapiens hg19 chr17 37881332 37881440 - TCTGCTCCTTGGTCCTTCACCTAACCT 0 ACATCCTCCAGGTAGCTCATCCCCTGG 0 - ILLUMINA NA 186 TRUE +SMAD4_1 SMAD4_1.chr18.48575169.48575170 SMAD4_1.chr18.48575169.48575170_tile_1 Homo sapiens hg19 chr18 48575169 48575170 - TACAAAAATTGAAACACTATTGAGATCCT 0 CGCATACTGACAATATTTAACATGTTTTAG 0 - ILLUMINA NA 172 TRUE +SMAD4_2 SMAD4_2.chr18.48581198.48581198 SMAD4_2.chr18.48581198.48581198_tile_1 Homo sapiens hg19 chr18 48581198 48581198 - ATGTTGGGAAAGTTGGCAGTGCTGGTA 0 CAAAGTCATGCACATATTCATCCTTCAC 0 - ILLUMINA NA 180 TRUE +SMAD4_3 SMAD4_3.chr18.48584560.48584560 SMAD4_3.chr18.48584560.48584560_tile_1 Homo sapiens hg19 chr18 48584560 48584560 - GCTGTCTAAAAATTAAGGCCCACATGG 0 TGATGCTATCTGCAACAGTCCTTCAC 0 - ILLUMINA NA 188 TRUE +SMAD4_4 SMAD4_4.chr18.48586262.48586262 SMAD4_4.chr18.48586262.48586262_tile_1 Homo sapiens hg19 chr18 48586262 48586262 - ACTCATGTCATGATGAGTATTGTACTC 0 AATGCAAGCTCATTGTGAACAGGCCCT 0 - ILLUMINA NA 184 TRUE +SMAD4_5 SMAD4_5.chr18.48591826.48591919 SMAD4_5.chr18.48591826.48591919_tile_1 Homo sapiens hg19 chr18 48591826 48591919 - CAATACCTTGCTCTCTCAATGGCTTCT 0 AGTAAGCAATGGAACACCAATACTCAG 0 - ILLUMINA NA 188 TRUE +SMAD4_11 SMAD4_11.chr18.48593405.48593405 SMAD4_11.chr18.48593405.48593405_tile_1 Homo sapiens hg19 chr18 48593405 48593405 - GCACTTGGGTAGATCTTATGAACAGCA 0 TGCCTATGTGCAACCTTAGGAAGAAA 0 - ILLUMINA NA 172 TRUE +SMAD4_12 SMAD4_12.chr18.48603032.48603094 SMAD4_12.chr18.48603032.48603094_tile_1 Homo sapiens hg19 chr18 48603032 48603094 - AAAGAATGAAAAGCATACTTACTGATAGC 0 CTGACGCAAATCAAAGACCTTTTAAGAA 0 - ILLUMINA NA 172 TRUE +SMAD4_15 SMAD4_15.chr18.48604668.48604754 SMAD4_15.chr18.48604668.48604754_tile_1 Homo sapiens hg19 chr18 48604668 48604754 - GCATGGTATGAAGTACTTCGTCTAGGA 0 AAGGTCATCAACACCAATTCCAGCAG 0 - ILLUMINA NA 172 TRUE +STK11_1 STK11_1.chr19.1207021.1207092 STK11_1.chr19.1207021.1207092_tile_1 Homo sapiens hg19 chr19 1207021 1207092 - CGCAACTTCTTCTTCTTGAGGATCTTG 0 TAGATGACCTCGGTGGAGTCGATGCGG 0 - ILLUMINA NA 178 TRUE +STK11_4 STK11_4.chr19.1220487.1220502 STK11_4.chr19.1220487.1220502_tile_1 Homo sapiens hg19 chr19 1220487 1220502 - AAAGCCGGGGAGCCCTGGCTGGTC 0 AGATTTTGAGGGTGCCACCGGTGGTG 0 - ILLUMINA NA 181 TRUE +STK11_8 STK11_8.chr19.1221264.1221319 STK11_8.chr19.1221264.1221319_tile_1 Homo sapiens hg19 chr19 1221264 1221319 + TGTACCCCTTCGAAGGGGACAACATCTA 0 GCTTTTGTGCAGAAATGTAGGGTTGG 0 + ILLUMINA NA 177 TRUE +STK11_12 STK11_12.chr19.1223059.1223125 STK11_12.chr19.1223059.1223125_tile_1 Homo sapiens hg19 chr19 1223059 1223125 - ACATCCTGGCCGAGTCAGCAGAGCC 0 ACCGGTCCTTGGTGTCTGGGCTC 0 - ILLUMINA NA 188 TRUE +JAK3_1 JAK3_1.chr19.17945696.17945696 JAK3_1.chr19.17945696.17945696_tile_1 Homo sapiens hg19 chr19 17945696 17945696 - ATCCCTGATCCCACTTTCATTCCCTCA 0 ATGCCCATCAGTGCCCTGGATCCTG 0 - ILLUMINA NA 176 TRUE +JAK3_2 JAK3_2.chr19.17948009.17948009 JAK3_2.chr19.17948009.17948009_tile_1 Homo sapiens hg19 chr19 17948009 17948009 - TAGTGCTGTGTGCACTAATGGCAGACT 0 AGCTTGATGAGCCAAGTGTCGTAC 0 - ILLUMINA NA 190 TRUE +SRC SRC.chr20.36031762.36031762 SRC.chr20.36031762.36031762_tile_1 Homo sapiens hg19 chr20 36031762 36031762 - AAAGAGGAAGGGCCTCGCCCCTGGCAAT 0 TACTGGGGCTCGGTGGACGTGAAGTAG 0 - ILLUMINA NA 191 TRUE +GNAS1 GNAS1.chr20.57484420.57484421 GNAS1.chr20.57484420.57484421_tile_1 Homo sapiens hg19 chr20 57484420 57484421 - ACAGCTGGTTATTCCAGAGGGACTGGG 0 GCGAAGCAGGTCCTGAAACAAAATTGA 0 - ILLUMINA NA 172 TRUE +SMARCB1_1 SMARCB1_1.chr22.24133967.24133990 SMARCB1_1.chr22.24133967.24133990_tile_1 Homo sapiens hg19 chr22 24133967 24133990 - GCGAGTGGTTTTGAAACAGGTTTACA 0 ACATACGGAGGTAGTTTCCCACCTAT 0 - ILLUMINA NA 189 TRUE +SMARCB1_3 SMARCB1_3.chr22.24143240.24143240 SMARCB1_3.chr22.24143240.24143240_tile_1 Homo sapiens hg19 chr22 24143240 24143240 - TTGTGGGGAGCACAAGGTCAAAGCAG 0 ATGCGGTTCCTGTTGATGGTTGTGGA 0 - ILLUMINA NA 175 TRUE +SMARCB1_4 SMARCB1_4.chr22.24145582.24145582 SMARCB1_4.chr22.24145582.24145582_tile_1 Homo sapiens hg19 chr22 24145582 24145582 - ATGTCCTGCGTGTCAGGTCCAGAATCT 0 TTCTGCCCATCGATCTCCATGTCCAG 0 - ILLUMINA NA 176 TRUE +SMARCB1_5_6 SMARCB1_5_6.chr22.24176352.24176357 SMARCB1_5_6.chr22.24176352.24176357_tile_1 Homo sapiens hg19 chr22 24176352 24176357 - ACTCCACCCCCACCCGATCCTCAGGA 0 TGTTGGCAAGACGCCTCATCCGCCTGG 0 - ILLUMINA NA 173 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_1 Homo sapiens hg19 chr19 3114942 3115070 + AGTGCGCGGTCCACCCCCTCCT 0 CTGCCCACCCAGCAGGACGTGCT 0 + ILLUMINA NA 182 TRUE +GNA11_4 GNA11_4.chr19.3114942.3115070 GNA11_4.chr19.3114942.3115070_tile_2 Homo sapiens hg19 chr19 3114942 3115070 - CGGCACACCGGGCAAATGAGCC 0 TAGCCCAAGGTGGCGATGCGGTC 0 - ILLUMINA NA 177 TRUE +GNA11_5 GNA11_5.chr19.3118922.3119051 GNA11_5.chr19.3118922.3119051_tile_1 Homo sapiens hg19 chr19 3118922 3119051 + TCCTGCTCCAGCCGATGTCAGTCT 0 GATCCACTGCTTTGAGAACGTGACAT 0 + ILLUMINA NA 189 TRUE +GNA11_6 GNA11_6.chr19.3119204.3119357 GNA11_6.chr19.3119204.3119357_tile_2 Homo sapiens hg19 chr19 3119204 3119357 + GGATGGAGGAGAGCAAAGCCCTGTT 0 CATGGGGAGGGGCTCGCGGGCA 0 + ILLUMINA NA 189 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_1 Homo sapiens hg19 chr19 3120987 3121177 - AACATCTTCAGGATGAACTCCCGCGCC 0 ACGGCCCACCCAGCTCGACCCCC 0 - ILLUMINA NA 172 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_2 Homo sapiens hg19 chr19 3120987 3121177 + AGGTCCCCAGCGGGACGCCCAG 0 CAGCTCAACCTCAAGGAGTACAACCT 0 + ILLUMINA NA 187 TRUE +GNA11_7 GNA11_7.chr19.3120987.3121177 GNA11_7.chr19.3120987.3121177_tile_3 Homo sapiens hg19 chr19 3120987 3121177 - AAAAATCTCCTCCCGCGGGCAGAG 0 AGGATGGTGTCCTTCACGGCCGC 0 - ILLUMINA NA 185 TRUE +GNAQ_4 GNAQ_4.chr9.80412436.80412564 GNAQ_4.chr9.80412436.80412564_tile_1 Homo sapiens hg19 chr9 80412436 80412564 - CATTCTCATTGTGTCTTCCCTCCTCTA 0 GTAACTGAGTCCATGAAACCTATTTCC 0 - ILLUMINA NA 188 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_1 Homo sapiens hg19 chr9 80409379 80409508 - GCTTAGTGAATATGATCAAGTTCTCGTGG 0 GCTTTCTTGAAATTTGATTTTAGGACTTTT 0 - ILLUMINA NA 174 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_2 Homo sapiens hg19 chr9 80409379 80409508 + AGATAATAAAATGATAATCCATTGCCTGTC 0 TTGGCCCCCTACATCGACCATTCT 0 + ILLUMINA NA 177 TRUE +GNAQ_5 GNAQ_5.chr9.80409379.80409508 GNAQ_5.chr9.80409379.80409508_tile_3 Homo sapiens hg19 chr9 80409379 80409508 - ATTGAATTGACTTGGATGATCATCGTC 0 GGTCAGAGAGAAGAAAATGGATACACT 0 - ILLUMINA NA 182 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_1 Homo sapiens hg19 chr9 80343430 80343583 - GAAAATCATGTATTCCCATCTAGTCGACT 0 TTGCCCTGTGCAGCCTGCGTGTTGA 0 - ILLUMINA NA 172 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_2 Homo sapiens hg19 chr9 80343430 80343583 + TTCACAGCTACTGAGCTGTGGTATGA 0 AGGGGTATGTGATAATTGTTCTAAAGAGAG 0 + ILLUMINA NA 171 TRUE +GNAQ_6 GNAQ_6.chr9.80343430.80343583 GNAQ_6.chr9.80343430.80343583_tile_3 Homo sapiens hg19 chr9 80343430 80343583 - GGTCGTATACAAAAGATGGGTTGGACTTAT 0 GTTCCAGAACTCCTCGGTTATTCTGTT 0 - ILLUMINA NA 187 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_1 Homo sapiens hg19 chr9 80336240 80336429 - ACCATCCTCCAGTTGAACCTGAAGG 0 TTTATTGCCGTCCTGGACTCTGTGTGAGCG 0 - ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_2 Homo sapiens hg19 chr9 80336240 80336429 + CAGGGAAGGGCAGGGCGGGTGTCTA 0 ATAATTTTGTCACTGTCTGGGTTCAGG 0 + ILLUMINA NA 172 TRUE +GNAQ_7 GNAQ_7.chr9.80336240.80336429 GNAQ_7.chr9.80336240.80336429_tile_3 Homo sapiens hg19 chr9 80336240 80336429 - CCAATGATGATTGAATACATTAGCAGAT 0 TACTCCCACTTCACGTGCGCCACAGAC 0 - ILLUMINA NA 177 TRUE +[Targets] +TargetA TargetB Target Number Chromosome Start Position End Position Probe Strand Sequence Species Build ID +MPL1_2.chr1.43815008.43815009_tile_1 MPL1_2.chr1.43815008.43815009_tile_1 1 chr1 43814982 43815163 + GGTGGCAGTTTCCTGCACACTACAGGTACCGCCCCCGCCAGGCAGGAGACTGGCGGTGGACCAGGTGGAGCCGAAGGCCTGTAAACAGGCATTCTTGGTTCGCTCTGTGACCCCAGATCTCCGTCCACCGCC Homo sapiens hg19 +NRAS1_7.chr1.115256528.115256531_tile_1 NRAS1_7.chr1.115256528.115256531_tile_1 1 chr1 115256500 115256680 + TCTTGTCCAGCTGTATCCAGTATGTCCAACAAACAGGTTTCACCATCTATAACCACTTGTTTTCTGTAAGAATCCTGGGGGTGTGGAGGGTAAGGGGGCAGGGAGGGAGGGAAGTTCAATTTTTATTA Homo sapiens hg19 +NRAS8_13.chr1.115258730.115258748_tile_1 NRAS8_13.chr1.115258730.115258748_tile_1 1 chr1 115258702 115258884 + TGCGCTTTTCCCAACACCACCTGCTCCAACCACCACCAGTTTGTACTCAGTCATTTCACACCAGCAAGAACCTGTTGGAAACCAGTAATCAGGGTTAATTGGCGAGCCACATCTACAGTACTTTAAAG Homo sapiens hg19 +ALK1.chr2.29432664.29432664_tile_1 ALK1.chr2.29432664.29432664_tile_1 1 chr2 29432636 29432822 + TCGGGCCATCCCGAAGTCTCCAATCTTGGCCACTCTTCCAGGGCCTGGACAGGTCAAGAGGCAGTTTCTGGCAGCAATGTCTCTGGGAAGAAAGGAAATGCATTTCCTAATTTTATCCCTAGGAAGATGAGTG Homo sapiens hg19 +ALK2.chr2.29443695.29443695_tile_1 ALK2.chr2.29443695.29443695_tile_1 1 chr2 29443667 29443836 + GTTGAATTTGCTGCAGAGCAGAGAGGGATGTAACCAAAATTAACTGAGCTGAGTCTGGGCAAATCTTAAACTGGGAGGAACAGGATACAAAGTTACATTTTCAGCAGCTACAATGTATA Homo sapiens hg19 +IDH1_1_2.chr2.209113112.209113113_tile_1 IDH1_1_2.chr2.209113112.209113113_tile_1 1 chr2 209113084 209113264 + ACGACCTATGATGATAGGTTTTACCCATCCACTCACAAGCCGGGGGATATTTTTGCAGATAATGGCTTCTCTGAAGACCGTGCCACCCAGAATATTTCGTATGGTGCCATTTGGTGATTTCCACATT Homo sapiens hg19 +ERBB4_1_2.chr2.212288942.212288955_tile_1 ERBB4_1_2.chr2.212288942.212288955_tile_1 1 chr2 212288912 212289100 + CCTTTCTCTAATAAATCAGGGATTTCTCGCGTTGGAATTCCATCATAGGGTTTTCCTCCAAAGGTCATCAGTTCCCATATAGTAACTCCTATATTGGAGAAAAAATTCTTACTTAAGCATATTAACAACATATGT Homo sapiens hg19 +ERBB4_3_4.chr2.212530066.212530135_tile_1 ERBB4_3_4.chr2.212530066.212530135_tile_1 1 chr2 212530036 212530210 + TGGATGGCATGGGTGGCACTCCCGATCTGGATCAGCATACTTGAAAATGAAACTGTTTGCCCCCTGTAAGCCATCTGGACATTTTTCCACACAGTTTGGGCCATCTTTAAAATGAGAGCACT Homo sapiens hg19 +ERBB4_5.chr2.212576857.212576857_tile_1 ERBB4_5.chr2.212576857.212576857_tile_1 1 chr2 212576821 212576990 + AATCCACAGTCTGAGCTGACATCAATGATCCTGTGCCAATGCCATCACAAGCTGTAGAAACAAGACTCAGAGTTAGGGGATTGAGAAACTTATTTTTGGCCAATAAATCA Homo sapiens hg19 +ERBB4_6_7.chr2.212578341.212578349_tile_1 ERBB4_6_7.chr2.212578341.212578349_tile_1 1 chr2 212578315 212578499 + CGCACACAAGAACTGGAATCTACCACAAAGTTATCTGATTAAAAAAAAAAAAAAGGTAAAATAAGCATTAATGTTAACATTCAGCAAACAAGCTCAAAACAAGATATTTTAGGGTTTAAAAATGATTAGCA Homo sapiens hg19 +ERBB4_8.chr2.212587147.212587147_tile_1 ERBB4_8.chr2.212587147.212587147_tile_1 1 chr2 212587115 212587285 + CTCCATATGTGTACTTTGCATTGAAATTGTGCTCCAGTTGAAAGGTGGTTGGATTGTAGACAAAGGTTTGGGGACACTGAGTAACACATGCTCCACTGTCATTGAAATTCATGCAGG Homo sapiens hg19 +ERBB4_9.chr2.212589811.212589811_tile_1 ERBB4_9.chr2.212589811.212589811_tile_1 1 chr2 212589783 212589957 + TGTGTCCTTAGGTCCTGAGCAGCCTCCAGCACATTCTCGATGGCAGCAGTCACTGACGTAAGGTCCGTAGCATCTGCCGTCACATTGTTCTGCACACACCGTCCTTGTCACTGCAGAAGAC Homo sapiens hg19 +ERBB4_10.chr2.212652764.212652764_tile_1 ERBB4_10.chr2.212652764.212652764_tile_1 1 chr2 212652706 212652876 + ATAATTCTACTTACATCCTGAACTACCATTTGTTGACACAAGAGTCAAGTTGGAAGGCCATGGGTTCCGAACAATATCTTGCCAATGAATGGTGTCTGCATAACAAAGGAATTT Homo sapiens hg19 +ERBB4_11.chr2.212812157.212812157_tile_1 ERBB4_11.chr2.212812157.212812157_tile_1 1 chr2 212812127 212812311 + TGTCAAGTTCTTTAATCCAAGTTCTTGAAGTCCAAAGTTTCCATCTTTTCTGTAGTTTAAAAATATTGCCAAGGCATATCGATCCTCATAAAGTTTTGTCCCACGAATAATGCGTAAATTCTCCAGAGG Homo sapiens hg19 +VHL1_2.chr3.10183797.10183817_tile_1 VHL1_2.chr3.10183797.10183817_tile_1 1 chr3 10183769 10183952 + GGCTCAACTTCGACGGCGAGCCGCAGCCCTACCCAACGCTGCCGCCTGGCACGGGCCGCCGCATCCACAGCTACCGAGGTACGGGCCCGGCGCTTAGGCCCGACCCAGCAGGGACGATAGCACGGTCTGAAGC Homo sapiens hg19 +VHL3_5.chr3.10188245.10188301_tile_1 VHL3_5.chr3.10188245.10188301_tile_1 1 chr3 10188217 10188401 + GGTTAACCAAACTGAATTATTTGTGCCATCTCTCAATGTTGACGGACAGCCTATTTTTGCCAATATCACACTGCCAGGTACTGACGTTTTACTTTTTAAAAAGATAAGGTTGTTGTGGTAAGTACAGGATA Homo sapiens hg19 +VHL6_8.chr3.10191480.10191506_tile_1 VHL6_8.chr3.10191480.10191506_tile_1 1 chr3 10191450 10191634 + TCTGAAAGAGCGATGCCTCCAGGTTGTCCGGAGCCTAGTCAAGCCTGAGAATTACAGGAGACTGGACATCGTCAGGTCGCTCTACGAAGATCTGGAAGACCACCCAAATGTGCAGAAAGACCTGGAGCGG Homo sapiens hg19 +MLH1.chr3.37067240.37067240_tile_1 MLH1.chr3.37067240.37067240_tile_1 1 chr3 37067212 37067394 + GGTTCGTACAGATTCCCGGGAACAGAAGCTTGATGCATTTCTGCAGCCTCTGAGCAAACCCCTGTCCAGTCAGCCCCAGGCCATTGTCACAGAGGATAAGACAGATATTTCTAGTGGCAGGGCTAGGCAG Homo sapiens hg19 +CTNNB1_1_16.chr3.41266040.41266137_tile_1 CTNNB1_1_16.chr3.41266040.41266137_tile_1 1 chr3 41266010 41266180 + ATGGCCATGGAACCAGACAGAAAAGCGGCTGTTAGTCACTGGCAGCAACAGTCTTACCTGGACTCTGGAATCCATTCTGGTGCCACTACCACAGCTCCTTCTCTGAGTGGTAAAGGC Homo sapiens hg19 +PIK3CA1.chr3.178916876.178916876_tile_1 PIK3CA1.chr3.178916876.178916876_tile_1 1 chr3 178916836 178917024 + TGATGAAACAAGACGACTTTGTGACCTTCGGCTTTTTCAACCCTTTTTAAAAGTAATTGAACCAGTAGGCAACCGTGAAGAAAAGATCCTCAATCGAGAAATTGGTATGATACAATATCCTATTCTAAAATGCAAA Homo sapiens hg19 +PIK3CA2.chr3.178921553.178921553_tile_1 PIK3CA2.chr3.178921553.178921553_tile_1 1 chr3 178921525 178921709 + ATGTAAATATTCGAGACATTGATAAGGTAAAGTCAAATGCTGATGCTTATTATTTTATAGAAATTATTTTAGATAACCTTTTTCTTGCACTATACAGTAATCTGTTGACCTGTAGTATGTTTTCAGATGGT Homo sapiens hg19 +PIK3CA3.chr3.178927980.178927980_tile_1 PIK3CA3.chr3.178927980.178927980_tile_1 1 chr3 178927906 178928082 + TTATAATTTAGACTAGTGAATATTTTTCTTTGTTTTTTAAGGAACACTGTCCATTGGCATGGGGAAATATAAACTTGTTTGATTACACAGACACTCTAGTATCTGGAAAAATGGCTTTGAATC Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 1 chr3 178936044 178936214 + ATCCTCTCTCTGAAATCACTGAGCAGGAGAAAGATTTTCTATGGAGTCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGAATTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 1 chr3 178938832 178939004 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTCTCAAACAGGAGAAGAAGGATGAAACACAAAAGGTGTGTGACTCTAGTTTGTGTTTGAGACTCTT Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_1 PIK3CA13_20.chr3.178952007.178952150_tile_1 1 chr3 178951881 178952054 + TATCTAGCTATTCGACAGCATGCCAATCTCTTCATAAATCTTTTCTCAATGATGCTTGGCTCTGGAATGCCAGAACTACAATCTTTTGATGACATTGCATACATTCGAAAGACCCTAGCC Homo sapiens hg19 +PIK3CA13_20.chr3.178952007.178952150_tile_2 PIK3CA13_20.chr3.178952007.178952150_tile_2 1 chr3 178951999 178952184 - TTTCAGTTCAATGCATGCTGTTTAATTGTGTGGAAGATCCAATCCATTTTTGTTGTCCAGCCACCATGATGTGCATCATTCATTTGTTTCATGAAATACTCCAAAGCCTCTTGCTCAGTTTTATCTAAG Homo sapiens hg19 +FGFR3_1_2.chr4.1803564.1803568_tile_1 FGFR3_1_2.chr4.1803564.1803568_tile_1 1 chr4 1803538 1803712 + GCGCTCCCCGCACCGGCCCATCCTGCAGGCGGGGCTGCCGGCCAACCAGACGGCGGTGCTGGGCAGCGACGTGGAGTTCCACTGCAAGGTGTACAGTGACGCACAGCCCCACATCCAGTGGCT Homo sapiens hg19 +FGFR3_3_4.chr4.1806119.1806153_tile_1 FGFR3_3_4.chr4.1806119.1806153_tile_1 1 chr4 1806091 1806277 + CGGGGTGGGCTTCTTCCTGTTCATCCTGGTGGTGGCGGCTGTGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAAGGCCTGGGCTCCCCCACCGTGCACAAGATCTCCCGCTTCCCGCTCAAGCGACAGGTA Homo sapiens hg19 +FGFR3_5_7.chr4.1807862.1807890_tile_1 FGFR3_5_7.chr4.1807862.1807890_tile_1 1 chr4 1807836 1808025 + CCGGGACGTGCACAACCTCGACTACTACAAGAAGACGACCAACGTGAGCCCGGCCCTGGGGTGCGGGGGTGGGGGTCATGCCAGTAGGACGCCTGGCGCCAACACCGCCTTCCCACACCCTCCCAGGGCCGGCTGCCCGTGA Homo sapiens hg19 +FGFR3_8.chr4.1808331.1808331_tile_1 FGFR3_8.chr4.1808331.1808331_tile_1 1 chr4 1808295 1808464 + GCTCCCCGTACCCCGGCATCCCTGTGGAGGAGCTCTTCAAGCTGCTGAAGGAGGGCCACCGCATGGACAAGCCCGCCAACTGCACACACGACCTGTGAGTGGCATCCCTGGCCCTCCACTGGGTCC Homo sapiens hg19 +FGFR3_9.chr4.1808949.1808949_tile_1 FGFR3_9.chr4.1808949.1808949_tile_1 1 chr4 1808921 1809105 + CCTGCTGCCCCCGGCCCCACCCAGCAGTGGGGGCTCGCGGACGTGAAGGGCCACTGGTCCCCAACAATGTGAGGGGTCCCTAGCAGCCCACCCTGCTGCTGGTGCACAGCCACTCCCCGGCATGAGACTCAGTGC Homo sapiens hg19 +PDGFRA1_4.chr4.55141013.55141049_tile_1 PDGFRA1_4.chr4.55141013.55141049_tile_1 1 chr4 55140981 55141157 + AAACCGAGGTATGAAATTCGCTGGAGGGTCATTGAATCAATCAGCCCAGATGGACATGAATATATTTATGTGGACCCGATGCAGCTGCCTTATGACTCAAGATGGGAGTTTCCAAGAGATGGA Homo sapiens hg19 +PDGFRA5.chr4.55144146.55144146_tile_1 PDGFRA5.chr4.55144146.55144146_tile_1 1 chr4 55144120 55144306 + AACTTGCTGGGAGCCTGCACCAAGTCAGGTGGGCTCACTGACCTGGAGTGAGGATTTTCACTGGACACATGTGGTTGTGAAAACTGTTCAATCAGGCTTAAATCCTCCACTCTCCATCCCCACACATGGCAGGG Homo sapiens hg19 +PDGFRA6.chr4.55144547.55144547_tile_1 PDGFRA6.chr4.55144547.55144547_tile_1 1 chr4 55144519 55144703 + CACAGAGTATTGCTTCTATGGAGATTTGGTCAACTATTTGCATAAGAATAGGGATAGCTTCCTGAGCCACCACCCAGAGAAGCCAAAGAAAGAGCTGGATATCTTTGGATTGAACCCTGCTGATGAAAGCAC Homo sapiens hg19 +PDGFRA7_23.chr4.55152040.55152109_tile_1 PDGFRA7_23.chr4.55152040.55152109_tile_1 1 chr4 55152012 55152184 + CGTCCTCCTGGCACAAGGAAAAATTGTGAAGATCTGTGACTTTGGCCTGGCCAGAGACATCATGCATGATTCGAACTATGTGTCGAAAGGCAGTGTACGTCCTCACTTCCCTCACTGGTCA Homo sapiens hg19 +KIT1.chr4.55561764.55561764_tile_1 KIT1.chr4.55561764.55561764_tile_1 1 chr4 55561736 55561913 + CGACGAGATTAGGCTGTTATGCACTGATCCGGGCTTTGTCAAATGGACTTTTGAGATCCTGGATGAAACGAATGAGAATAAGCAGAATGAATGGATCACGGAAAAGGCAGAAGCCACCAACACCG Homo sapiens hg19 +KIT2.chr4.55592185.55592186_tile_1 KIT2.chr4.55592185.55592186_tile_1 1 chr4 55592155 55592341 + CCTATTTTAACTTTGCATTTAAAGGTAACAACAAAGGTATATTTCTTTTTAATCCAATTTAAGGGGATGTTTAGGCTCTGTCTACCATATCAGTCATGATTTTAAGTTCATTCCAACATTGACCATGTCATTTC Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_1 KIT3_19.chr4.55593464.55593689_tile_1 1 chr4 55593342 55593512 + ATTTCTCTTCCATTGTAGAGCAAATCCATCCCCACACCCTGTTCACTCCTTTGCTGATTGGTTTCGTAATCGTAGCTGGCATGATGTGCATTATTGTGATGATTCTGACCTACAAATA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_2 KIT3_19.chr4.55593464.55593689_tile_2 1 chr4 55593436 55593609 - TTCTGTGGGGAGAAAGGGAAAAATAGATCACCTTTTAATAATTATTGTCTCAGTCATTAGAGCACTCTGGAGAGAGAACAAATAAATGGTTACCTGTAAATATTTGTAGGTCAGAATCATCA Homo sapiens hg19 +KIT3_19.chr4.55593464.55593689_tile_3 KIT3_19.chr4.55593464.55593689_tile_3 1 chr4 55593556 55593739 + AACCCATGTATGAAGTACAGTGGAAGGTTGTTGAGGAGATAAATGGAAACAATTATGTTTACATAGACCCAACACAACTTCCTTATGATCACAAATGGGAGTTTCCCAGAAACAGGCTGAGTTTTGGTCAG Homo sapiens hg19 +KIT20_21.chr4.55594221.55594258_tile_1 KIT20_21.chr4.55594221.55594258_tile_1 1 chr4 55594193 55594380 + CAAAGTCCTGAGTTACCTTGGTAATCACATGAATATTGTGAATCTACTTGGAGCCTGCACCATTGGAGGTAAAGCCGTGTCCAAGCTGCCTTTTATTGTCTGTCAGGTTATCAAAACATGACATTTTAATATG Homo sapiens hg19 +KIT22.chr4.55595519.55595519_tile_1 KIT22.chr4.55595519.55595519_tile_1 1 chr4 55595493 55595675 + CAGAATATTGTTGCTATGGTGATCTTTTGAATTTTTTGAGAAGAAAACGTGATTCATTTATTTGTTCAAAGCAGGAAGATCATGCAGAAGCTGCACTTTATAAGAATCTTCTGCATTCAAAGGAGTCT Homo sapiens hg19 +KIT23.chr4.55597495.55597497_tile_1 KIT23.chr4.55597495.55597497_tile_1 1 chr4 55597467 55597652 + CAGCGATAGTACTAATGAGTACATGGACATGAAACCTGGAGTTTCTTATGTTGTCCCAACCAAGGCCGACAAAAGGAGATCTGTGAGAATAGGTGAGTACCTACCTATCAAGCAACCAAGAGTAACTTTAC Homo sapiens hg19 +KIT24_28.chr4.55599320.55599348_tile_1 KIT24_28.chr4.55599320.55599348_tile_1 1 chr4 55599290 55599472 + AGAGACATCAAGAATGATTCTAATTATGTGGTTAAAGGAAACGTGAGTACCCATTCTCTGCTTGACAGTCCTGCAAAGGATTTTTAGTTTCAACTTTCGATAAAAATTGTTTCCTGTGATTTTCATAAT Homo sapiens hg19 +KIT29.chr4.55602694.55602694_tile_1 KIT29.chr4.55602694.55602694_tile_1 1 chr4 55602666 55602850 + CCTGAAAGCATTTTCAACTGTGTATACACGTTTGAAAGTGACGTCTGGTCCTATGGGATTTTTCTTTGGGAGCTGTTCTCTTTAGGTAAAATGATCCTTGCCAAAGACAACTTCATTAGACTCAGAGCATCTT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_1 KDR1.chr4.55946114.55946257_tile_1 1 chr4 55945984 55946155 + CGGCTACTTCCTGCTGGTGGAAAGAACAACACTTGAAAATCTGAGCAGCACCTCTCATGTGATGTCCAGGAGTTGGGGGTGTGGATGCTTCCTTTTAAACAGGAGGAGAGCT Homo sapiens hg19 +KDR1.chr4.55946114.55946257_tile_2 KDR1.chr4.55946114.55946257_tile_2 1 chr4 55946098 55946284 - GGATATCACTCCGATGACACAGACACCACCGTGTACTCCAGTGAGGAAGCAGAACTTTTAAAGCTGATAGAGATTGGAGTGCAAACCGGTAGCACAGCCCAGATTCTCCAGCCTGACTCGGGGACCACACTGA Homo sapiens hg19 +KDR3.chr4.55953807.55953807_tile_1 KDR3.chr4.55953807.55953807_tile_1 1 chr4 55953777 55953965 + TTGGGGTCACATACTTCCTCCTCCTCCATACAGGAAACAGGTGAGGTAGGCAGAGAGAGTCCAGAATCCTCTTCCATGCTCAAAGTCTCTGATATCGGAAGAACAATGTAGTCTTTGCCATCCTGAAACAATAAA Homo sapiens hg19 +KDR4.chr4.55955111.55955127_tile_1 KDR4.chr4.55955111.55955127_tile_1 1 chr4 55955085 55955257 + CCCCGTGCCAGCAGTCCAGCATGGTCTGGTACCTAGAGAAGCAAAACACTGATTTCATTAAATGCCTCTTTCTTCCTGAATGCTGAAAATAAGCACTTAAATGAGTACACATTTGTAAAGAG Homo sapiens hg19 +KDR6.chr4.55960989.55961023_tile_1 KDR6.chr4.55960989.55961023_tile_1 1 chr4 55960959 55961129 + TCACTGAGGGACTTCTCCTCCACAAATCCAGAGCTGGCTGAGCTCTGGCTACTGGTGATGCTGTCCAAGCGCCGTTTCAGATCCACAGGGATTGCTCCAACGTAGTCTTTCCCTTGA Homo sapiens hg19 +KDR8.chr4.55962507.55962507_tile_1 KDR8.chr4.55962507.55962507_tile_1 1 chr4 55962477 55962653 + GCTCCTTCTACAAATACAGTACAAAGAGGGAAATCATAGGTATGGACATTTCCTTCAATAATTGGGGTCCCTCCCTCCCTGCATGCCACTATACAACTTACCCTCCGGGGTAACACAGCTGTGA Homo sapiens hg19 +KDR9.chr4.55972964.55972964_tile_1 KDR9.chr4.55972964.55972964_tile_1 1 chr4 55972936 55973106 + ACTGAGACAGCTTGGCTATAAGAAAGAGATAACAGCGCATATTATGATTTAATTTTTCTTTAATTAGAGTCAAGAGTAAGGAAAAGATTCAGACTTTGGTTATTCTGTTCTTAGAAA Homo sapiens hg19 +KDR10.chr4.55979623.55979623_tile_1 KDR10.chr4.55979623.55979623_tile_1 1 chr4 55979595 55979775 + CTCGGTTTACAAGTTTCTTATGCTGATGCTGAAAAAAAGAGTTGACTGAACTTCCAAAGCACAGCATATAACATTACCCAATAACTTCTAGTAACACACAGAATTAAATCTGGGCTTTGGTAAACATT Homo sapiens hg19 +KDR11.chr4.55980348.55980348_tile_1 KDR11.chr4.55980348.55980348_tile_1 1 chr4 55980320 55980496 + TGCTGTACAATTTAAGACAAGCTTTTCTCCAACAGATAGTTCAATTCCATGAGACGGACTCAGAACCACATCATAAATCCTATACCCTAGAGCAAGTAAATTGAAAAAACAGAACATGAGAGA Homo sapiens hg19 +FBXW7_1.chr4.153245446.153245446_tile_1 FBXW7_1.chr4.153245446.153245446_tile_1 1 chr4 153245416 153245604 + AACGACTGGTGCCCTGTTAACGTGTGAATGCAATTCCCTGTCTCCACATCCCAAACACGGATTGATGTATCAAGAGATCCACTCACCACATGGATACCATCAAACTACAAAAGACACAGTTTATTAGAATAGA Homo sapiens hg19 +FBXW7_2.chr4.153247288.153247366_tile_1 FBXW7_2.chr4.153247288.153247366_tile_1 1 chr4 153247248 153247417 + TTGAACACAGCGGACTGCTGCAACATGACCCATCAAAACATGTAAACACTGGCCTGTCTCAATATCCCAAACCCTAAGAGTGGCATCTCGAGAACCGCTAACAACTCTGCAG Homo sapiens hg19 +FBXW7_5.chr4.153249384.153249384_tile_1 FBXW7_5.chr4.153249384.153249384_tile_1 1 chr4 153249338 153249520 + TTCATGAAGATGCATACAACGCACAGTGGAAGTATGCCCATATAAGGTGTGTATACATTCTCCAGTCTCTGCATTCCACACTTTGAGTGTCCGATCTGTAGATCCACTAATGATGATGTTGTCTCTCAT Homo sapiens hg19 +FBXW7_7.chr4.153250883.153250883_tile_1 FBXW7_7.chr4.153250883.153250883_tile_1 1 chr4 153250853 153251031 + ATTCGGTTACCACAAAACTGTAAGCATGTGATCACATGATCATCATGTCCTTTCAGCACCTATAAGAAAGATGTGCAGATTAGAAATATGTTAATTAAATTATGTTCTTTAAAATACTGGTGAAGA Homo sapiens hg19 +FBXW7_8.chr4.153258983.153258983_tile_1 FBXW7_8.chr4.153258983.153258983_tile_1 1 chr4 153258953 153259142 + TCGTTGAAACTGGGGTTCTATCACTTGCATCATATGTTTTACTTGTGTTGGTTCACAACTATCAATGAGTTCATCTAAAGCAAGCAATTTCTCTGGTCCACTCCAGCTCTATCAAAGAGAATTAGAAATTTT Homo sapiens hg19 +APC1.chr5.112173917.112173917_tile_1 APC1.chr5.112173917.112173917_tile_1 1 chr5 112173887 112174071 + AAGCGAGGTTTGCAGATCTCCACCACTGCAGCCCAGATTGCCAAAGTCATGGAAGAAGTGTCAGCCATTCATACCTCTCAGGAAGACAGAAGTTCTGGGTCTACCACTGAATTACATTGTGTGACAGATGA Homo sapiens hg19 +APC2.chr5.112174631.112174631_tile_1 APC2.chr5.112174631.112174631_tile_1 1 chr5 112174603 112174775 + TCGAGTGGGTTCTAATCATGGAATTAATCAAAATGTAAGCCAGTCTTTGTGTCAAGAAGATGACTATGAAGATGATAAGCCTACCAATTATAGTGAACGTTACTCTGAAGAAGAACAGC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_1 APC3_42.chr5.112175162.112175958_tile_1 1 chr5 112175034 112175208 - TCTGCTTCCTGTGTCGTCTGATTACATCCTATTTCATCTTCAGCTGATGACAAAGATGATAATGAACTACATCTTGAAAAACATATTGGAGTATCTTCTACACAATAAGTCTGTATTGTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_2 APC3_42.chr5.112175162.112175958_tile_2 1 chr5 112175128 112175297 + ATGTAATCAGACGACACAGGAAGCAGATTCTGCTAATACCCTGCAAATAGCAGAAATAAAAGAAAAGATTGGAACTAGGTCAGCTGAAGATCCTGTGAGCGAAGTTCCAGCAGTGTCAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_3 APC3_42.chr5.112175162.112175958_tile_3 1 chr5 112175216 112175386 - CCTGAAGAAAATTCAACAGCTTTGTGCCTGGCTGATTCTGAAGATAAACTAGAACCCTGCAGTCTGCTGGATTTGGTTCTAGGGTGCTGTGACACTGCTGGAACTTCGCTCACAGGAT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_4 APC3_42.chr5.112175162.112175958_tile_4 1 chr5 112175306 112175475 + CACAAAGCTGTTGAATTTTCTTCAGGAGCGAAATCTCCCTCCAAAAGTGGTGCTCAGACACCCAAAAGTCCACCTGAACACTATGTTCAGGAGACCCCACTCATGTTTAGCA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_5 APC3_42.chr5.112175162.112175958_tile_5 1 chr5 112175394 112175566 - GCCACTTACCATTCCACTGCATGGTTCACTCTGAACGGAGCTGGCAATCGAACGACTCTCAAAACTATCAAGTGAACTGACAGAAGTACATCTGCTAAACATGAGTGGGGTCTCCTGAAC Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_6 APC3_42.chr5.112175162.112175958_tile_6 1 chr5 112175512 112175683 + GCATTATAAGCCCCAGTGATCTTCCAGATAGCCCTGGACAAACCATGCCACCAAGCAGAAGTAAAACACCTCCACCACCTCCTCAAACAGCTCAAACCAAGCGAGAAGTACCTAAAAATA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_7 APC3_42.chr5.112175162.112175958_tile_7 1 chr5 112175630 112175799 - CCGTGGCAAAATGTAATAAAGTATCAGCATCTGGAAGAACCTGGACCCTCTGAACTGCAGCATTTACTGCAGCTTGCTTAGGTCCACTCTCTCTCTTTTCAGCAGTAGGTGCTTT Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_8 APC3_42.chr5.112175162.112175958_tile_8 1 chr5 112175740 112175911 + GGAAAGTACTCCAGATGGATTTTCTTGTTCATCCAGCCTGAGTGCTCTGAGCCTCGATGAGCCATTTATACAGAAAGATGTGGAATTAAGAATAATGCCTCCAGTTCAGGAA Homo sapiens hg19 +APC3_42.chr5.112175162.112175958_tile_9 APC3_42.chr5.112175162.112175958_tile_9 1 chr5 112175854 112176042 - AGTATTTCAATATCATCATCATCTGAATCATCTAATAGGTCCTTTTCAGAATCAATAGTTTTTTCTGCCTCTTTCTCTTGGTTTTCATTTGATTCTTTAGGCTGCTCTGATTCTGTTTCATTCCCATTGTCATTT Homo sapiens hg19 +CSF1R1_3.chr5.149433644.149433646_tile_1 CSF1R1_3.chr5.149433644.149433646_tile_1 1 chr5 149433616 149433799 + GATAGTTGTTGGGCTGCAGCAAGGGCTGGGCGATATCCCCTTGCTCGCAGCAGGTCAGGTGCTCACTAGAGCTCTCCTCCTCCAGCTCACTGCTGCTGCTGCCGCTGCCACCGCTTCTGCTGCTGCTCGGC Homo sapiens hg19 +CSF1R4.chr5.149453044.149453044_tile_1 CSF1R4.chr5.149453044.149453044_tile_1 1 chr5 149453016 149453189 + CAAGTAGGCACTCTCTGGAAAGCAGAACACACAAGCATCTGGCATTAGTGGGAAGATGTCCTTGTTTATTTGTCCATTTTGTCATCCACCCATTGATCCAGTCCCTGAGCAGCTATGTCAC Homo sapiens hg19 +NPM1.chr5.170837547.170837548_tile_1 NPM1.chr5.170837547.170837548_tile_1 1 chr5 170837493 170837677 + TTTTTTTTCCAGGCTATTCAAGATCTCTGGCAGTGGAGGAAGTCTCTTTAAGAAAATAGTTTAAACAATTTGTTAAAAAATTTTCCGTCTTATTTCATTTCTGTAACAGTTGATATCTGGCTGTCCTTTTTA Homo sapiens hg19 +EGFR1.chr7.55211080.55211080_tile_1 EGFR1.chr7.55211080.55211080_tile_1 1 chr7 55211052 55211238 + AGAGGAAATATGTACTACGAAAATTCCTATGCCTTAGCAGTCTTATCTAACTATGATGCAAATAAAACCGGACTGAAGGAGCTGCCCATGAGAAATTTACAGGGTGAGAGGCTGGGATGCCAAGGCTGGGGGT Homo sapiens hg19 +EGFR2.chr7.55221822.55221822_tile_1 EGFR2.chr7.55221822.55221822_tile_1 1 chr7 55221792 55221964 + GGTGCCACCTGCGTGAAGAAGTGTCCCCGTGAGTCCTCCTCTGTGGGCCCTCTAACTGGTCAGGCATCCTTGTCCCGCTCTGTCTCCTGCTGAGCCCTGGAGTATCCCATCTTGGAGAGT Homo sapiens hg19 +EGFR3.chr7.55233043.55233043_tile_1 EGFR3.chr7.55233043.55233043_tile_1 1 chr7 55233019 55233203 + GGAGTCATGGGAGAAAACAACACCCTGGTCTGGAAGTACGCAGACGCCGGCCATGTGTGCCACCTGTGCCATCCAAACTGCACCTACGGGTGAGTGGAAAGTGAAGGAGAACAGAACATTTCCTCTCTTGCAAAT Homo sapiens hg19 +EGFR4.chr7.55241677.55241708_tile_1 EGFR4.chr7.55241677.55241708_tile_1 1 chr7 55241649 55241827 + AGGAAACTGAATTCAAAAAGATCAAAGTGCTGGGCTCCGGTGCGTTCGGCACGGTGTATAAGGTAAGGTCCCTGGCACAGGCCTCTGGGCTGGGCCGCAGGGCCTCTCATGGTCTGGTGGGGAGCC Homo sapiens hg19 +EGFR9.chr7.55242418.55242511_tile_1 EGFR9.chr7.55242418.55242511_tile_1 1 chr7 55242388 55242576 + GACTCTGGATCCCAGAAGGTGAGAAAGTTAAAATTCCCGTCGCTATCAAGGAATTAAGAGAAGCAACATCTCCGAAAGCCAACAAGGAAATCCTCGATGTGAGTTTCTGCTTTGCTGTGTGGGGGTCCATGGCT Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_1 EGFR44.chr7.55249005.55249131_tile_1 1 chr7 55248879 55249052 + TCTTCACCTGGAAGGGGTCCATGTGCCCCTCCTTCTGGCCACCATGCGAAGCCACACTGACGTGCCTCTCCCTCCCTCCAGGAAGCCTACGTGATGGCCAGCGTGGACAACCCCCACGTGTG Homo sapiens hg19 +EGFR44.chr7.55249005.55249131_tile_2 EGFR44.chr7.55249005.55249131_tile_2 1 chr7 55249003 55249178 - CAGTTGAGCAGGTACTGGGAGCCAATATTGTCTTTGTGTTCCCGGACATAGTCCAGGAGGCAGCCGAAGGGCATGAGCTGCGTGATGAGCTGCACGGTGGAGGTGAGGCAGATGCCCAGCAGGCGGC Homo sapiens hg19 +EGFR54.chr7.55259514.55259524_tile_1 EGFR54.chr7.55259514.55259524_tile_1 1 chr7 55259486 55259662 + GCTGGCCAAACTGCTGGGTGCGGAAGAGAAAGAATACCATGCAGAAGGAGGCAAAGTAAGGAGGTGGCTTTAGGTCAGCCAGCATTTTCCTGACACCAGGGACCAGGCTGCCTTCCCACTAGC Homo sapiens hg19 +MET1.chr7.116339642.116339642_tile_1 MET1.chr7.116339642.116339642_tile_1 1 chr7 116339614 116339792 + AGCCCAGCCAGTGTCCTGACTGTGTGGTGAGCGCCCTGGGAGCCAAAGTCCTTTCATCTGTAAAGGACCGGTTCATCAACTTCTTTGTAGGCAATACCATAAATTCTTCTTATTTCCCAGATCAT Homo sapiens hg19 +MET2.chr7.116340262.116340262_tile_1 MET2.chr7.116340262.116340262_tile_1 1 chr7 116340234 116340420 + AACAAGATCGTCAACAAAAACAATGTGAGATGTCTCCAGCATTTTTACGGACCCAATCATGAGCACTGCTTTAATAGGGTAAGTCACATCAGTTCCCCACTTATAAACTGTGAGGTATAAATTAGAAATAAGT Homo sapiens hg19 +MET3.chr7.116411990.116411990_tile_1 MET3.chr7.116411990.116411990_tile_1 1 chr7 116411958 116412127 + GCCCAACTACAGAAATGGTTTCAAATGAATCTGTAGACTACCGAGCTACTTTTCCAGAAGGTATATTTCAGTTTATTGTTCTGAGAAATACCTATACATATACCTCAGTGGGTTGT Homo sapiens hg19 +MET4.chr7.116417463.116417464_tile_1 MET4.chr7.116417463.116417464_tile_1 1 chr7 116417431 116417620 + TATATCATGGGACTTTGTTGGACAATGATGGCAAGAAAATTCACTGTGCTGTGAAATCCTTGAACAGTAAGTGGCATTTTATTTAACCATGGAGTATACTTTTGTGGTTTGCAACCTAATAAATAGCTTATAATA Homo sapiens hg19 +MET6.chr7.116423413.116423474_tile_1 MET6.chr7.116423413.116423474_tile_1 1 chr7 116423385 116423555 + TGTATGATAAAGAATACTATAGTGTACACAACAAAACAGGTGCAAAGCTGCCAGTGAAGTGGATGGCTTTGGAAAGTCTGCAAACTCAAAAGTTTACCACCAAGTCAGATGTGGTAAT Homo sapiens hg19 +SMO1.chr7.128845101.128845101_tile_1 SMO1.chr7.128845101.128845101_tile_1 1 chr7 128845073 128845257 + GGTTCGGACAGACAACCCCAAGAGCTGGTACGAGGACGTGGAGGGCTGCGGCATCCAGTGCCAGAACCCGCTCTTCACAGAGGCTGAGCACCAGGACATGCACAGCTACATCGCGGCCTTCGGGGCCGTCACGGGC Homo sapiens hg19 +SMO2.chr7.128846040.128846040_tile_1 SMO2.chr7.128846040.128846040_tile_1 1 chr7 128846010 128846194 + TACGCCCTGATGGCTGGTGTGGTTTGGTTTGTGGTCCTCACCTATGCCTGGCACACTTCCTTCAAAGCCCTGGGCACCACCTACCAGCCTCTCTCGGGCAAGACCTCCTACTTCCACCTGCTCACCTGGTC Homo sapiens hg19 +SMO3.chr7.128846374.128846374_tile_1 SMO3.chr7.128846374.128846374_tile_1 1 chr7 128846348 128846536 + CGTGCTGGCCCCAATCGGCCTGGTGCTCATCGTGGGAGGCTACTTCCTCATCCGAGGTGAGTGAAGACCAGGCCAGGACCAGTTGGGCAACAAAATATACTGGGCACTTGCTGCCAGTACTGGGAGCTGCCAGCACG Homo sapiens hg19 +SMO4.chr7.128850341.128850341_tile_1 SMO4.chr7.128850341.128850341_tile_1 1 chr7 128850311 128850499 + GCACCTGGGTCTGGACCAAGGCCACGCTGCTCATCTGGAGGCGTACCTGGTGCAGGTGGGCATGGCAGCCAGCCCCTCCTGCCCTGCCCGCCTCACCCTCAGCCTTGGGACCCCATCTTTAGGTTTTGTCGGGTCCTG Homo sapiens hg19 +SMO5.chr7.128851593.128851593_tile_1 SMO5.chr7.128851593.128851593_tile_1 1 chr7 128851563 128851734 + GTCACCCCTGTGGCAACTCCAGGTATGAGAGTTCAAGCTTCTGGAGGAAGGTGGGGGGAGCACAGAGGCTGGGGGCTTCTGGGACTGGAGTACAGGGGCTGTCGGAGGAGGAGGAAGAG Homo sapiens hg19 +BRAF1.chr7.140453121.140453193_tile_1 BRAF1.chr7.140453121.140453193_tile_1 1 chr7 140453093 140453267 + CACTCCATCGAGATTTCACTGTAGCTAGACCAAAATCACCTATTTTTACTGTGAGGTCTTCATGAAGAAATATATCTGAGGTGTAGTAAGTAAAGGAAAACAGTAGATCTCATTTTCCTATC Homo sapiens hg19 +BRAF28.chr7.140481397.140481478_tile_1 BRAF28.chr7.140481397.140481478_tile_1 1 chr7 140481369 140481545 + ACTGTTCCAAATGATCCAGATCCAATTCTTTGTCCCACTGTAATCTGCCCATCAGGAATCTCCCAATCATCACTCGAGTCCCGTCTACCAAGTGTTTTCTTGATAAAAACAGTAAAAAAGTCA Homo sapiens hg19 +FGFR1_1.chr8.38282209.38282209_tile_1 FGFR1_1.chr8.38282209.38282209_tile_1 1 chr8 38282183 38282360 + GGGGACCGCTCTGTGGAAGATGGGAGAGGAGGCACTTGTCATGGGGACCTTGCCATGGCTAAAGAGGGGTGGGCTCACCTGCGCCCCACTTGGCTTTCCCAGTGATGGGTTGTAAACCTCCCAGCAC Homo sapiens hg19 +FGFR1_2.chr8.38285938.38285938_tile_1 FGFR1_2.chr8.38285938.38285938_tile_1 1 chr8 38285908 38286090 + TCCGAGGAGGGGAGAGCATCTATGGGAAGAAGAAGGGGCACTGAGGTTCCTCCTAGGGACCCCTAGATTTCACCAAGGCTAGTGCAGTTCCAGATGAACACGGACACCCTCCCCATGGGGATCCCAGTC Homo sapiens hg19 +JAK2_1.chr9.5073769.5073770_tile_1 JAK2_1.chr9.5073769.5073770_tile_1 1 chr9 5073737 5073923 + TATGTGTCTGTGGAGACGAGAGTAAGTAAAACTACAGGCTTTCTAATGCCTTTCTCAGAGCATCTGTTTTTGTTTATATAGAAAATTCAGTTTCAGGATCACAGCTAGGTGTCAGTGTAAACTATAATTT Homo sapiens hg19 +CDKN2A1.chr9.21971153.21971187_tile_1 CDKN2A1.chr9.21971153.21971187_tile_1 1 chr9 21971123 21971308 + GGGCTCCGCGCCGTGGAGCAGCAGCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGCCAGGGTGGGGGCCGGCATGACGGAAAGGAAGCTTGTGTAGAGCCCCC Homo sapiens hg19 +ABL1_1.chr9.133738330.133738364_tile_1 ABL1_1.chr9.133738330.133738364_tile_1 1 chr9 133738302 133738491 + CCATGAAGCACAAGCTGGGCGGGGGCCAGTACGGGGAGGTGTACGAGGGCGTGTGGAAGAAATACAGCCTGACGGTGGCCGTGAAGACCTTGAAGGTAGGCTGGGACTGCCGGGGGTGCCCAGGGTACGTGGGGCAAG Homo sapiens hg19 +ABL1_9.chr9.133747520.133747520_tile_1 ABL1_9.chr9.133747520.133747520_tile_1 1 chr9 133747476 133747664 + TTTCCTTCTGCAGGAGGACACCATGGAGGTGGAAGAGTTCTTGAAAGAAGCTGCAGTCATGAAAGAGATCAAACACCCTAACCTGGTGCAGCTCCTTGGTGAGTAAGCCCGGGGCTCTGAAGAGAGGGTCTCGCGCCGC Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_1 ABL1_10.chr9.133748283.133748414_tile_1 1 chr9 133748157 133748327 - CCCGTAGGTCATGAACTCAGTGATGATATAGAACGGGGGCTCCCGGGTGCAGACCCCTGCCAACAAGACAACGAGGACTTCAACACGTGGCTCCGCTCCCAACTGAACAAACAACT Homo sapiens hg19 +ABL1_10.chr9.133748283.133748414_tile_2 ABL1_10.chr9.133748283.133748414_tile_2 1 chr9 133748277 133748457 + GAACCTCCTGGACTACCTGAGGGAGTGCAACCGGCAGGAGGTGAACGCCGTGGTGCTGCTGTACATGGCCACTCAGATCTCGTCAGCCATGGAGTACCTGGAGAAGAAAAACTTCATCCACAGGTAGGGGCCT Homo sapiens hg19 +ABL1_16.chr9.133750356.133750356_tile_1 ABL1_16.chr9.133750356.133750356_tile_1 1 chr9 133750328 133750516 + GCCCATGCTGGAGCCAAGTTCCCCATCAAATGGACTGCACCCGAGAGCCTGGCCTACAACAAGTTCTCCATCAAGTCCGACGTCTGGGGTAAGGGCTGCTGCTGCACTGAAGTGGTCCTTCCTGACTACAGGAGGGTT Homo sapiens hg19 +NOTCH1_1.chr9.139397768.139397768_tile_1 NOTCH1_1.chr9.139397768.139397768_tile_1 1 chr9 139397740 139397928 + CCAGGTAGACGATGGAGCTGGGCGGACAATCAGAGAGGGGCTGGGACCCGAGGCTTCCTCCTCCCCCGCCCACCGGCCAGGGATGCTGCCGCAGGACACTGAGGCCCATGACGCCACAGTCAGGACATGGTGAGGC Homo sapiens hg19 +NOTCH1_2.chr9.139399344.139399422_tile_1 NOTCH1_2.chr9.139399344.139399422_tile_1 1 chr9 139399316 139399485 + GCAGCACGCGGCTGAGCTCCCGCAGGAAGTGGAAGGAGCTGTTGCGCAGCTGCTCCGGCGGCATCAGCACCACCACCACCAGCGTGCCGGCCGCCAGCCTCTCGGGTACATGCTCCGC Homo sapiens hg19 +RET1.chr10.43609078.43609104_tile_1 RET1.chr10.43609078.43609104_tile_1 1 chr10 43609048 43609226 + CTGCTTCCCTGAGGAGGAGAAGTGCTTCTGCGAGCCCGAAGACATCCAGGGTGAGTGGGTGGCGGCCGGGACCACCACCACCTCCCAGCCCCACAGAGGTCTCAACAGCACATCTGAGGTCCCAACAA Homo sapiens hg19 +RET2_9.chr10.43609940.43609950_tile_1 RET2_9.chr10.43609940.43609950_tile_1 1 chr10 43609902 43610075 - TGGCTTGTGGGCAAACTTGTGGTAGCAGTGGATGCAGAAGGCAGACAGCAGCACCGAGACGATGAAGGAGAAGAGGACAGCGGCTGCGATCACCGTGCGGCACAGCTCGTCGCACAGTGG Homo sapiens hg19 +RET10.chr10.43613840.43613840_tile_1 RET10.chr10.43613840.43613840_tile_1 1 chr10 43613810 43613998 + CGAGTGAGCTGCGAGACCTGCTGTCAGAGTTCAACGTCCTGAAGCAGGTCAACCACCCACATGTCATCAAATTGTATGGGGCCTGCAGCCAGGATGGTAAGGCCAGCTGCAGGGTGAGGTGGGCAGCCACTGCACCCAG Homo sapiens hg19 +RET11_12.chr10.43615567.43615569_tile_1 RET11_12.chr10.43615567.43615569_tile_1 1 chr10 43615533 43615703 + CCTGGTAGCTGAGGGGCGGAAGATGAAGATTTCGGATTTCGGCTTGTCCCGAGATGTTTATGAAGAGGATTCCTACGTGAAGAGGAGCCAGGTGCCCAGTCCCGGGGATGAGGCGGGG Homo sapiens hg19 +RET13.chr10.43617416.43617416_tile_1 RET13.chr10.43617416.43617416_tile_1 1 chr10 43617388 43617564 + ATGGCAATTGAATCCCTTTTTGATCATATCTACACCACGCAAAGTGATGTGTAAGTGTGGGTGTTGCTCTCTTGGGGTGGAGGTTACAGAAACACCCTTATACATGTAGTGGGGCCACGACGC Homo sapiens hg19 +PTEN1.chr10.89624242.89624244_tile_1 PTEN1.chr10.89624242.89624244_tile_1 1 chr10 89624214 89624388 + CAAAGAGATCGTTAGCAGAAACAAAAGGAGATATCAAGAGGATGGATTCGACTTAGACTTGACCTGTATCCATTTCTGCGGCTGCTCCTCTTTACCTTTCTGTCACTCTCTTAGAACGTGG Homo sapiens hg19 +PTEN3.chr10.89685307.89685307_tile_1 PTEN3.chr10.89685307.89685307_tile_1 1 chr10 89685275 89685459 + ATATACAATCTGTAAGTATGTTTTCTTATTTGTATGCTTGCAAATATCTTCTAAAACAACTATTAAGTGAAAGTTATCTGCTTGTTAGAGTGAGGTAGAGTTAAAGATACATTTTAACAGAATTGTATT Homo sapiens hg19 +PTEN4.chr10.89711893.89711900_tile_1 PTEN4.chr10.89711893.89711900_tile_1 1 chr10 89711865 89712039 + GTCAGAGGCGCTATGTGTATTATTATAGCTACCTGTTAAAGAATCATCTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN7.chr10.89717615.89717772_tile_1 1 chr10 89717489 89717668 + ATATTGCTGATATTAATCATTAAAATCGTTTTTGACAGTTTGACAGTTAAAGGCATTTCCTGTGAAATAATACTGGTATGTATTTAACCATGCAGATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_2 PTEN7.chr10.89717615.89717772_tile_2 1 chr10 89717615 89717801 - TTTAGCATCTTGTTCTGTTTGTGGAAGAACTCTACTTTGATATCACCACACACAGGTAACGGCTGAGGGAACTCAAAGTACATGAACTTGTCTTCCCGTCGTGTGGGTCCTGAATTGGAGGAATATATCTTCACC Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 1 chr10 89720684 89720870 + CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATCGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAATATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_2 PTEN13.chr10.89720716.89720852_tile_2 1 chr10 89720814 89720991 - TTCTTCATCAGCTGTACTCCTAGAATTAAACACACATCACATACATACAAGTCAACAACCCCCACAAAATGTTTAATTTAACTGACCTTAAAATTTGGAGAAAAGTATCGGTTGGCTTT Homo sapiens hg19 +FGFR2_1.chr10.123258034.123258034_tile_1 FGFR2_1.chr10.123258034.123258034_tile_1 1 chr10 123258006 123258184 + GATTTATGATATTCTTGTGTTTCCCAATCATCTTCATCATCTCCATCTCTGACACCAGATCAGAAAGGTCTTTCTCTGTGGCATCATCTATGAACAGTAGGCATATTCACAAATCAGTTCATTTC Homo sapiens hg19 +FGFR2_2.chr10.123274774.123274803_tile_1 FGFR2_2.chr10.123274774.123274803_tile_1 1 chr10 123274746 123274930 + CAGTAAATGGCTATCTCCAGGTAGTCTGGGGAAGCTGTAATCTCCTTTTCTCTTCCAGGCGCTAGATTGCAGATCACAGGAGGAGGAACAGATAAGCAGGCCATAGAGTTAGCACACCAGACTGACGCATC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_1 FGFR2_5.chr10.123279503.123279677_tile_1 1 chr10 123279385 123279555 + AACAGGAAATCAAAGAACCTGTGGCCAAACCCATGAAGGAGACCCCAGTTGTGGGTACCTTTAGATTCAGAAAGTCCTCACCTTGAGAACCTTGAGGTAGGGCAGCCCGTCGGGCCC Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_2 FGFR2_5.chr10.123279503.123279677_tile_2 1 chr10 123279471 123279640 - ACGTAGAGTTTGTCTGCAAGGTTTACAGTGATGCCCAGCCCCACATCCAGTGGATCAAGCACGTGGAAAAGAACGGCAGTAAATACGGGCCCGACGGGCTGCCCTACCTCAAGGTT Homo sapiens hg19 +FGFR2_5.chr10.123279503.123279677_tile_3 FGFR2_5.chr10.123279503.123279677_tile_3 1 chr10 123279587 123279769 + TCTCCTCCGACCACTGTGGAGGCATTTGCCGGCAGTCCGGCTTGGAGGATGGGCCGGTGAGGCGATCGCTCTGGTGGAGAGAGGGAAGAAAGGAGGAGTGGGGATGGGAGAATGAGAGACCAATAAATA Homo sapiens hg19 +HRAS1.chr11.533873.533875_tile_1 HRAS1.chr11.533873.533875_tile_1 1 chr11 533843 534021 + CCTCCTGGCCGGCGGTATCCAGGATGTCCAACAGGCACGTCTCCCCATCAATGACCACCTGCTTCCGGTAGGAATCCTGCAGGAGGACAGGGCTCAGGGACCCCCTCAGGACCTTCCGTGGGGGGA Homo sapiens hg19 +HRAS6.chr11.534285.534289_tile_1 HRAS6.chr11.534285.534289_tile_1 1 chr11 534251 534434 + GCCCACACCGCCGGCGCCCACCACCACCAGCTTATATTCCGTCATCGCTCCTCAGGGGCCTGCGGCCCGGGGTCCTCCTACAGGGTCTCCTGCCCCACCTGCCAAGGAGGGCCCTGCTCAGCCAGGCCCAGGC Homo sapiens hg19 +ATM1.chr11.108117847.108117848_tile_1 ATM1.chr11.108117847.108117848_tile_1 1 chr11 108117817 108117989 + TGTCACCAGGTACAGTAAGTAGGTCATGTCACATTTAGAAATTTCCTGTTAATTTTTTTTTTAAACTGGGCATTTTGGGCTTTTAAAACCTGTGTTCTCACAAAAAGCCTATAAAAT Homo sapiens hg19 +ATM2.chr11.108119823.108119823_tile_1 ATM2.chr11.108119823.108119823_tile_1 1 chr11 108119793 108119963 + TTGTGCCTTGGTAAAGTGTTACCATTTTCTCATTCAGTGTCATTTTAATCTCTTGTATGTTATTTTTCAGAAAACTTTCAGTGGAATCCTTTCATCTCAACCAGAACTAAGTCATTT Homo sapiens hg19 +ATM3.chr11.108123551.108123551_tile_1 ATM3.chr11.108123551.108123551_tile_1 1 chr11 108123513 108123683 + AGTAATTTTCCTCATCTTGTACTGGAGAAAATTCTTGTGAGTCTCACTATGAAAAACTGTAAAGCTGCAATGAATTTTTTCCAAAGCGTGCCAGAATGGTATGTTATCTAATA Homo sapiens hg19 +ATM4.chr11.108137973.108138003_tile_1 ATM4.chr11.108137973.108138003_tile_1 1 chr11 108137939 108138126 + TAATGGAGGTGGAGGATCAGTCATCCATGAATCTATTTAACGATTACCCTGATAGTAGTGTTAGTGATGCAAACGAACCTGGAGAGAGCCAAAGTACCATAGGTAAATACATATTTACTACTTGGGATT Homo sapiens hg19 +ATM6.chr11.108155132.108155132_tile_1 ATM6.chr11.108155132.108155132_tile_1 1 chr11 108155104 108155281 + GGCACAGCAAAGAGAGACTGCTACCAAGGTCTATGATATGCTTAAAAGTGAAAACTTATTGGGAAAACAGGTATGGCTTCAATTTTTATGTACTTTTCATTCCCTGAATGATATGAGATAT Homo sapiens hg19 +ATM7.chr11.108170476.108170479_tile_1 ATM7.chr11.108170476.108170479_tile_1 1 chr11 108170442 108170618 + GGGTCCTATAGATTTCTCTACCATAGCTATACAACATAGTAAAGATGCATCTTATACCAAGGCCCTTAAGTTATTTGAAGATAAAGAACTTCAGTGGACCTTCATAATGCTGACCTACCTGAA Homo sapiens hg19 +ATM9.chr11.108172421.108172421_tile_1 ATM9.chr11.108172421.108172421_tile_1 1 chr11 108172391 108172571 + TTAGCCACAAAGACTGGACATAGTTTCTGGGAGATTTATAAGATGACAACAGATCCAATGCTGGCCTATCTACAGCCTTTTAGAACATCAAGAAAAAAGGTCTCTTAAGTAATAAATGTTTATTGAA Homo sapiens hg19 +ATM10.chr11.108173640.108173640_tile_1 ATM10.chr11.108173640.108173640_tile_1 1 chr11 108173612 108173801 + AAATCTGTGGATTCCTCTAAGTGAAAATCATGACATTTGGATAAAGACACTGACTTGTGCTTTTTTGGACAGTGGAGGCACAAAATGTGAAATTCTTCAATTATTAAAGCCAATGTGTGAAGTAAGAAGATTAATT Homo sapiens hg19 +ATM11.chr11.108180945.108180945_tile_1 ATM11.chr11.108180945.108180945_tile_1 1 chr11 108180915 108181101 + AAGTTGCCAAGGTAGCTCAGTCTTGTGCTGCTCACTTTACAGCTTTACTCTATGCAGAAATCTATGCAGATAAGAAAAGTATGGATGATCAAGAGAAAAGGTAATGGAATTTAGAATTTTTGGTTTTTAAAA Homo sapiens hg19 +ATM12.chr11.108200958.108200961_tile_1 ATM12.chr11.108200958.108200961_tile_1 1 chr11 108200926 108201096 + TTCAGCGAGAGCTGGAGTTGGATGAATTAGCCCTGCGTGCACTGAAAGAGGATCGTAAACGCTTCTTATGTAAAGCAGTTGAAAATTATATCAACTGCTTATTAAGTGGAGAAGA Homo sapiens hg19 +ATM14.chr11.108204681.108204681_tile_1 ATM14.chr11.108204681.108204681_tile_1 1 chr11 108204651 108204823 + TACTATGGAAATTAAGGTAATTTGCAATTAACTCTTGATTTTTTTTAAACTAAATTTTTTTTATTAGATTGAACCATTTGAAATAGTATTTTTATGTAGGTCAAAATTGGTTAAATA Homo sapiens hg19 +ATM15.chr11.108205769.108205769_tile_1 ATM15.chr11.108205769.108205769_tile_1 1 chr11 108205739 108205928 + AGGTGTAAATTTACCAAAAATAATAGATTGTGTAGGTTCCGATGGCAAGGAGAGGAGACAGCTTGTTAAGGTGAGCCTTCCCTTCTCTGGCTTAGCCCTTAGAGTTTTAGTGATGAAAATTTTTAGTTCATATT Homo sapiens hg19 +ATM16.chr11.108206594.108206594_tile_1 ATM16.chr11.108206594.108206594_tile_1 1 chr11 108206566 108206750 + GATGCTGTCATGCAACAGGTCTTCCAGATGTGTAATACATTACTGCAGAGAAACACGGAAACTAGGAAGAGGAAATTAACTATCTGTACTTATAAGGTAACTATTTGTACTTCTGTTAGTTCACCAAAAAC Homo sapiens hg19 +ATM17.chr11.108218089.108218089_tile_1 ATM17.chr11.108218089.108218089_tile_1 1 chr11 108218061 108218247 + TCTAGGTAAGTAATAAAATCTATGTATCTATTCTTTTTAGTAAATATTTGGTCATCATGGAATGTTGTTTGCCTACCAAGATATTACAAATATAAGAGACAGATAAATTGAAGCAGTAAATATTGGGTTTTTT Homo sapiens hg19 +ATM18.chr11.108225590.108225590_tile_1 ATM18.chr11.108225590.108225590_tile_1 1 chr11 108225562 108225751 + AACCATTGTAGAGGTAAAGTATTTTATAAGGAAGACTTTATTTTTTTTCTTACCAGGTAGACTGTGTATCTCATCAGGAAGTCACTGATGTGAAGAGCACTGCTTCATTTTAACATAGGGGGATGTGGCTGGGCAGC Homo sapiens hg19 +ATM19.chr11.108236086.108236203_tile_1 ATM19.chr11.108236086.108236203_tile_1 1 chr11 108236058 108236241 + ACGTGTCTTAATGAGACTACAAGAGAAACTGAAAGGAGTGGAAGAAGGCACTGTGCTCAGTGTTGGTGGACAAGTGAATTTGCTCATACAGCAGGCCATAGACCCCAAAAATCTCAGCCGACTTTTCCCAG Homo sapiens hg19 +KRAS1.chr12.25378562.25378562_tile_1 KRAS1.chr12.25378562.25378562_tile_1 1 chr12 25378532 25378717 + TTGCTGATGTTTCAATAAAAGGAATTCCATAACTTCTTGCTAAGTCCTGAGCCTGTTTTGTGTCTACTGTTCTAGAAGGCAAATCACATTTATTTCCTACTAGGACCATAGGTACATCTTCAGAGTCCTTA Homo sapiens hg19 +KRAS2.chr12.25380275.25380283_tile_1 KRAS2.chr12.25380275.25380283_tile_1 1 chr12 25380245 25380427 + CCTCTTGACCTGCTGTGTCGAGAATATCCAAGAGACAGGTTTCTCCATCAATTACTACTTGCTTCCTGTAGGAATCCTGAGAAGGGAGAAACACAGTCTGGATTATTACAGTGCACCTTTTACTTCAA Homo sapiens hg19 +KRAS7.chr12.25398255.25398285_tile_1 KRAS7.chr12.25398255.25398285_tile_1 1 chr12 25398225 25398414 + TGTATCGTCAAGGCACTCTTGCCTACGCCACCAGCTCCAACTACCACAAGTTTATATTCAGTCATTTTCAGCAGGCCTTATAATAAAAATAATGAAAATGTGACTATATTAGAACATGTCACACATAAGGTTA Homo sapiens hg19 +PTPN11_1.chr12.112888163.112888211_tile_1 PTPN11_1.chr12.112888163.112888211_tile_1 1 chr12 112888135 112888323 + TGGTGATTACTATGACCTGTATGGAGGGGAGAAATTTGCCACTTTGGCTGAGTTGGTCCAGTATTACATGGAACATCACGGGCAATTAAAAGAGAAGAATGGAGATGTCATTGAGCTTAAATATCCTCTGAACTGT Homo sapiens hg19 +PTPN11_10.chr12.112926884.112926888_tile_1 PTPN11_10.chr12.112926884.112926888_tile_1 1 chr12 112926856 112927032 + GGTCAGGGATGGTCCAGACAGAAGCACAGTACCGATTTATCTATATGGCGGTCCAGCATTATATTGAAACACTACAGCGCAGGATTGAAGAAGAGCAGGTACCAGCCTGAGGGCTGGCATGCGG Homo sapiens hg19 +HNF1A_1.chr12.121431413.121431414_tile_1 HNF1A_1.chr12.121431413.121431414_tile_1 1 chr12 121431385 121431558 + GTGGGGCCCAGCATCCCAGCAGATCCTGTTCCAGGCCTATGAGAGGCAGAAGAACCCTAGCAAGGAGGAGCGAGAGACGCTAGTGGAGGAGTGCAATAGGTACAACGGCGGGCGGGAAACAG Homo sapiens hg19 +HNF1A_3.chr12.121432070.121432070_tile_1 HNF1A_3.chr12.121432070.121432070_tile_1 1 chr12 121432042 121432221 + GCGCAAAGAAGAAGCCTTCCGGCACAAGCTGGCCATGGACACGTACAGCGGGCCCCCCCCAGGGCCAGGCCCGGGACCTGCGCTGCCCGCTCACAGCTCCCCTGGCCTGCCTCCACCTGCCCTCTCCCCC Homo sapiens hg19 +FLT3_1.chr13.28592620.28592653_tile_1 FLT3_1.chr13.28592620.28592653_tile_1 1 chr13 28592590 28592766 + CATAGTTGGAATCACTCATGATATCTCGAGCCAATCCAAAGTCACATATCTTCACCACTTTCCCGTGGGTGACAAGCACGTTCCTGGCGGCCAGGTCTCTGTGAACACACTGTCAAGAATGA Homo sapiens hg19 +FLT3_13.chr13.28602329.28602329_tile_1 FLT3_13.chr13.28602329.28602329_tile_1 1 chr13 28602295 28602464 + GTGTGCACGCCCCCAGCAGGTTCACAATATTCTCGTGGCTTCCCAGCTGGGTCATCATCTTGAGTTCTGACATGAGTGCCTCTCTTTCAGAGCTGTCTGCTTTTTCTGTCAAAGAA Homo sapiens hg19 +FLT3_14.chr13.28608244.28608341_tile_1 FLT3_14.chr13.28608244.28608341_tile_1 1 chr13 28608214 28608402 + ACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCATACCTAAATTGCTTCAGAGATGAAATGATGAGTCA Homo sapiens hg19 +FLT3_22.chr13.28610138.28610138_tile_1 FLT3_22.chr13.28610138.28610138_tile_1 1 chr13 28610098 28610267 - TATAGGAGTGAACCACTATGCCCAGCCAGTGAGCTTATTTCACACGTTCTTTTCTATAGGGAAACCTCAAGTGCTCGCAGAAGCATCGGCAAGTCAGGCGTCCTGTTTCTCGGATGG Homo sapiens hg19 +RB1_1.chr13.48919244.48919244_tile_1 RB1_1.chr13.48919244.48919244_tile_1 1 chr13 48919156 48919336 + ATTTACTTTTTTCTATTCTTTCCTTTGTAGTGTCCATAAATTCTTTAACTTACTAAAAGAAATTGATACCAGTACCAAAGTTGATAATGCTATGTCAAGACTGTTGAAGAAGTATGATGTATTG Homo sapiens hg19 +RB1_2.chr13.48923148.48923148_tile_1 RB1_2.chr13.48923148.48923148_tile_1 1 chr13 48923120 48923296 + TTATTAGCTAAAGGTAAGTTCATTATATTTATTAAATGCTAATATTTCAAATGTAATAATTAAATTGGCATTCCTTTGGACTAAATTCCCCAATTTTTATTGAGTAATGTACTCCTCCCTCAT Homo sapiens hg19 +RB1_3.chr13.48942685.48942685_tile_1 RB1_3.chr13.48942685.48942685_tile_1 1 chr13 48942655 48942826 + ACGAAAAAGTAACCTTGATGAAGAGGTGAATGTAATTCCTCCACACACTCCAGTTAGGTATGAATTTTCCTACTTTTAATTATATTATAATTTTGTTATTCATGGCTTTATAGTG Homo sapiens hg19 +RB1_4.chr13.48955538.48955550_tile_1 RB1_4.chr13.48955538.48955550_tile_1 1 chr13 48955504 48955684 + TAGAACGATGTGAACATCGAATCATGGAATCCCTTGCATGGCTCTCAGTAAGTAGCTAAATAATTGAAGAAATTCATTCATGTGCATATGGCTAACAAATTATTGTTAGTGAGAGGTGTTTCTTA Homo sapiens hg19 +RB1_6.chr13.49027168.49027168_tile_1 RB1_6.chr13.49027168.49027168_tile_1 1 chr13 49027112 49027288 + TTTGATCTTATTAAACAATCAAAGGACCGAGAAGGACCAACTGATCACCTTGAATCTGCTTGTCCTCTTAATCTTCCTCTCCAGAATAATCACACTGCAGCAGATATGTAAGCAAAATATA Homo sapiens hg19 +RB1_7.chr13.49033843.49033846_tile_1 RB1_7.chr13.49033843.49033846_tile_1 1 chr13 49033813 49033989 + TCTCCGGCTAAATACACTTTGTGAACGCCTTCTGTCTGAGCACCCAGAATTAGAACATATCATCTGGACCCTTTTCCAGCACACCCTGCAGAATGAGTATGAACTCATGAGAGACAGGCATTT Homo sapiens hg19 +RB1_8.chr13.49037877.49037877_tile_1 RB1_8.chr13.49037877.49037877_tile_1 1 chr13 49037815 49037985 + TTTACATCAATTTATTTACTAGATTATGATGTGTTCCATGTATGGCATATGCAAAGTGAAGAATATAGACCTTAAATTCAAAATCATTGTAACAGCATACAAGGATCTTCCTCA Homo sapiens hg19 +RB1_9.chr13.49039164.49039164_tile_1 RB1_9.chr13.49039164.49039164_tile_1 1 chr13 49039132 49039304 + AAGAGGAGTATGATTCTATTATAGTATTCTATAACTCGGTCTTCATGCAGAGACTGAAAACAAATATTTTGCAGTATGCTTCCACCAGGGTAGGTCAAAAGTATCCTTTGATTGGAAAA Homo sapiens hg19 +AKT1.chr14.105246455.105246455_tile_1 AKT1.chr14.105246455.105246455_tile_1 1 chr14 105246429 105246600 + CTCACGTTGGTCCACATCCTGCGGCCGCTCCTTGTAGCCAATGAAGGTGCCATCATTCTTGAGGAGGAAGTAGCGTGGCCGCCAGGTCTTGATGTACTCCCCTACAGACGTGCGGGTGGTGA Homo sapiens hg19 +CDH1_1.chr16.68835649.68835650_tile_1 CDH1_1.chr16.68835649.68835650_tile_1 1 chr16 68835613 68835782 + TGGGCACAGATGGTGTGATTACAGTCAAAAGGCCTCTACGGTTTCATAACCCACAGATCCATTTCTTGGTCTACGCCTGGGACTCCACCTACAGAAAGTTTTCCACCAAAGTCACGCTGAAT Homo sapiens hg19 +CDH1_2.chr16.68846137.68846137_tile_1 CDH1_2.chr16.68846137.68846137_tile_1 1 chr16 68846109 68846283 + CGATAATCCTCCGATCTTCAATCCCACCACGGTAATTCTATAACTCCTTAGAGGGTTTCCAAAGAAAGGTCTTTTGTTGTTCATGAACTAAGTGTCACCACTGCTCATGGGCGAAGTCTTT Homo sapiens hg19 +CDH1_3.chr16.68847274.68847277_tile_1 CDH1_3.chr16.68847274.68847277_tile_1 1 chr16 68847246 68847422 + ACTGATGCTGATGCCCCCAATACCCCAGCGTGGGAGGCTGTATACACCATATTGAATGATGATGGTGGACAATTTGTCGTCACCACAAATCCAGTGAACAACGATGGCATTTTGAAAACAGCA Homo sapiens hg19 +TP53_1.chr17.7574003.7574021_tile_1 TP53_1.chr17.7574003.7574021_tile_1 1 chr17 7573977 7574147 + CGGAACATCTCGAAGCGCTCACGCCCACGGATCTGCAGCAACAGAGGAGGGGGAGAAGTAAGTATATACACAGTACCTGAGTTAAAAGATGGTTCAAGTTACAATTGTTTGACTTTATG Homo sapiens hg19 +TP53_3.chr17.7577022.7577129_tile_1 TP53_3.chr17.7577022.7577129_tile_1 1 chr17 7576996 7577166 + CGCTTAGTGCTCCCTGGGGGCAGCTCGTGGTGAGGCTCCCCTTTCTTGCGGAGATTCTCTTCCTCTGTGCGCCGGTCTCTCCCAGGACAGGCACAAACACGCACCTCAAAGCTGTTCCG Homo sapiens hg19 +TP53_17.chr17.7577523.7577574_tile_1 TP53_17.chr17.7577523.7577574_tile_1 1 chr17 7577495 7577683 + GGTGAGGATGGGCCTCCGGTTCATGCCGCCCATGCAGGAACTGTTACACATGTAGTTGTAGTGGATGGTGGTACAGTCAGAGCCAACCTAGGAGATAACACAGGCCCAAGATGAGGCCAGTGCGCCTTGGGGAGA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_1 TP53_31_59.chr17.7578190.7578536_tile_1 1 chr17 7578064 7578234 + AGAAAGCCCCCCTACTGCTCACCTGGAGGGCCACTGACAACCACCCTTAACCCCTCCTCCCAGAGACCCCAGTTGCAAACCAGACCTCAGGCGGCTCATAGGGCACCACCACACTA Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_2 TP53_31_59.chr17.7578190.7578536_tile_2 1 chr17 7578156 7578325 - CTGATTGCTCTTAGGTCTGGCCCCTCCTCAGCATCTTATCCGAGTGGAAGGAAATTTGCGTGTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCC Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_3 TP53_31_59.chr17.7578190.7578536_tile_3 1 chr17 7578246 7578415 + TGAGGAGGGGCCAGACCTAAGAGCAATCAGTGAGGAATCAGAGGCCTGGGGACCCTGGGCAACCAGCCCTGTCGTCTCTCCAGCCCCAGCTGCTCACCATCGCTATCTGAGCAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_4 TP53_31_59.chr17.7578190.7578536_tile_4 1 chr17 7578346 7578515 - GTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAGTCACAGCACATGACGGAGGTTGTGAGGCGCTGCCCCCACCATGAGCGCTGCTCAGATAGCG Homo sapiens hg19 +TP53_31_59.chr17.7578190.7578536_tile_5 TP53_31_59.chr17.7578190.7578536_tile_5 1 chr17 7578468 7578645 + CCCACAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTAGGAAGAGGAAGGAGACAGAGTTGAAAGTCAGGGCACAAGTGAACAGATAAAGCAACTGGA Homo sapiens hg19 +TP53_60.chr17.7579358.7579403_tile_1 TP53_60.chr17.7579358.7579403_tile_1 1 chr17 7579324 7579507 + GCCCAGACGGAAACCGTAGCTGCCCTGGTAGGTTTTCTGGGAAGGGACAGAAGATGACAGGGGCCAGGAGGGGGCTGGTGCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGCAGGGGCCACGGGGGGAGCAG Homo sapiens hg19 +TP53_64.chr17.7579882.7579882_tile_1 TP53_64.chr17.7579882.7579882_tile_1 1 chr17 7579852 7580032 + GCTCGACGCTAGGATCTGACTGCGGCTCCTCCATGGCAGTGACCCGGAAGGCAGTCTGGCTGCTGCAAGAGGAAAAGTGGGGATCCAGCATGAGACACTTCCAACCCTGGGTCACCTGGGCCTGCAG Homo sapiens hg19 +ERBB2_1.chr17.37880219.37880261_tile_1 ERBB2_1.chr17.37880219.37880261_tile_1 1 chr17 37880191 37880361 + TGTTGAGGGAAAACACATCCCCCAAAGCCAACAAAGAAATCTTAGACGTAAGCCCCTCCACCCTCTCCTGCTAGGAGGACAGGAAGGACCCCATGGCTGCAGGTCTGGGCTCTGGTCT Homo sapiens hg19 +ERBB2_4.chr17.37880993.37881012_tile_1 ERBB2_4.chr17.37880993.37881012_tile_1 1 chr17 37880963 37881151 + CGTGATGGCTGGTGTGGGCTCCCCATATGTCTCCCGCCTTCTGGGCATCTGCCTGACATCCACGGTGCAGCTGGTGACACAGCTTATGCCCTATGGCTGCCTCTTAGACCATGTCCGGGAAAACCGCGGACGCCTGGG Homo sapiens hg19 +ERBB2_13.chr17.37881332.37881440_tile_1 ERBB2_13.chr17.37881332.37881440_tile_1 1 chr17 37881298 37881482 + GCGGCTCGTACACAGGGACTTGGCCGCTCGGAACGTGCTGGTCAAGAGTCCCAACCATGTCAAAATTACAGACTTCGGGCTGGCTCGGCTGCTGGACATTGACGAGACAGAGTACCATGCAGATGGGGGCA Homo sapiens hg19 +SMAD4_1.chr18.48575169.48575170_tile_1 SMAD4_1.chr18.48575169.48575170_tile_1 1 chr18 48575131 48575301 + TTTGACTTAAAATGTGATAGTGTCTGTGTGAATCCATATCACTACGAACGAGTTGTATCACCTGGAATTGGTAAGTAGACTTTGCTTTCATCCTAAGAAACATAAAGGGAAA Homo sapiens hg19 +SMAD4_2.chr18.48581198.48581198_tile_1 SMAD4_2.chr18.48581198.48581198_tile_1 1 chr18 48581168 48581346 + AGGGACAGCCATCGTTGTCCACTGAAGGACATTCAATTCAAACCATCCAGCATCCACCAAGTAATCGTGCATCGACAGAGACATACAGCACCCCAGCTCTGTTAGCCCCATCTGAGTCTAATGC Homo sapiens hg19 +SMAD4_3.chr18.48584560.48584560_tile_1 SMAD4_3.chr18.48584560.48584560_tile_1 1 chr18 48584528 48584714 + GGGCCTCAGCCAGGACAGCAGCAGAATGGATTTACTGGTCAGCCAGCTACTTACCATCATAGTATGTACATACTTTAAAAAATCTTTTAAATAGTTGAGAAAAAAGTAGGCAGCCTTTATAAAAGCAAATTAAC Homo sapiens hg19 +SMAD4_4.chr18.48586262.48586262_tile_1 SMAD4_4.chr18.48586262.48586262_tile_1 1 chr18 48586234 48586416 + CCAGCCTCCCATTTCCAATCATCCTGGTAAGTGTATTTCAAAATTGATTTCCTGTATTTAGATTGATTTAGTGGTGATTGAAACGCACAAACACAGGCTTTAATGGAATTATGGGGTCACTTCTCAGAT Homo sapiens hg19 +SMAD4_5.chr18.48591826.48591919_tile_1 SMAD4_5.chr18.48591826.48591919_tile_1 1 chr18 48591796 48591982 + TTGAAATGGATGTTCAGGTAGGAGAGACATTTAAGGTTCCTTCAAGCTGCCCTATTGTTACTGTTGATGGATACGTGGACCCTTCTGGAGGAGATCGCTTTTGTTTGGGTCAACTCTCCAATGTCCACAGGAC Homo sapiens hg19 +SMAD4_11.chr18.48593405.48593405_tile_1 SMAD4_11.chr18.48593405.48593405_tile_1 1 chr18 48593377 48593547 + AAGGTGTGCAGTTGGAATGTAAAGGTGAAGGTGATGTTTGGGTCAGGTGCCTTAGTGACCACGCGGTCTTTGTACAGAGTTACTACTTAGACAGAGAAGCTGGGCGTGCACCTGGAGA Homo sapiens hg19 +SMAD4_12.chr18.48603032.48603094_tile_1 SMAD4_12.chr18.48603032.48603094_tile_1 1 chr18 48602998 48603168 + TGTCATCGACAGATGCAGCAGCAGGCGGCTACTGCACAAGCTGCAGCAGCTGCCCAGGCAGCAGCCGTGGCAGGAAACATCCCTGGCCCAGGATCAGTAGGTGGAATAGCTCCA Homo sapiens hg19 +SMAD4_15.chr18.48604668.48604754_tile_1 SMAD4_15.chr18.48604668.48604754_tile_1 1 chr18 48604638 48604808 + CGTCGCTTATGCATACTCAGGATGAGTTTTGTGAAAGGCTGGGGACCGGATTACCCAAGACAGAGCATCAAAGAAACACCTTGCTGGATTGAAATTCACTTACACCGGGCCCTCCAGC Homo sapiens hg19 +STK11_1.chr19.1207021.1207092_tile_1 STK11_1.chr19.1207021.1207092_tile_1 1 chr19 1206993 1207169 + CCAGCCGCGCCGCAAGCGGGCCAAGCTCATCGGCAAGTACCTGATGGGGGACCTGCTGGGGGAAGGCTCTTACGGCAAGGTGAAGGAGGTGCTGGACTCGGAGACGCTGTGCAGGAGGGCCGT Homo sapiens hg19 +STK11_4.chr19.1220487.1220502_tile_1 STK11_4.chr19.1220487.1220502_tile_1 1 chr19 1220459 1220638 + CCGACCTGGGCGTGGCCGAGGTAGGCACGTGCTAGGGGGGGCCCTGGGGCGCCCCCTCCCGGGCACTCCCTGAGGGCTGCACGGCACCGCCACAGGCACTGCACCCGTTCGCGGCGGACGACACCTGCCG Homo sapiens hg19 +STK11_8.chr19.1221264.1221319_tile_1 STK11_8.chr19.1221264.1221319_tile_1 1 chr19 1221232 1221407 - CCCGCCTCCCTGGGGCTGCGGGCAGAGGGATGAGGCTCCCACCTTTCAGCAGGTCAGAGAGCGGGGGGCCACAGTCGCCCGGGATGGCGTAGCTCCCCTTCCCGATGTTCTCAAACAACTTG Homo sapiens hg19 +STK11_12.chr19.1223059.1223125_tile_1 STK11_12.chr19.1223059.1223125_tile_1 1 chr19 1223035 1223221 + GGCGCAGCATGACTGTGGTGCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACATCATCTACACTCAGGACTTCACGGTGCCCGGTGAGTCTGGCGGGGGCCCCTGCCC Homo sapiens hg19 +JAK3_1.chr19.17945696.17945696_tile_1 JAK3_1.chr19.17945696.17945696_tile_1 1 chr19 17945666 17945840 + GGTGACGCCACTAAACACTTCCCAGACCGTGGCGCCGAAGCCCCACTTGTCAGCTTCCAAGCTAAGTGTCTGCGCCTCCCGGAGACACTCGGGGGCCACCCAGGGGATCCTGTCGGTGAGCAC Homo sapiens hg19 +JAK3_2.chr19.17948009.17948009_tile_1 JAK3_2.chr19.17948009.17948009_tile_1 1 chr19 17947981 17948169 + CGCTGCTTCCAGGAATGACTGGGGAAGGTGGGAAGGGAGAGAAGATGCGTGGGTTTCTTCCACTCCAATAATCCCAAATTTTGTGCTCACAGACCTGCCTTAGGGGAACACCTGGCCACAGGTCACCTTTGGCCCTGG Homo sapiens hg19 +SRC.chr20.36031762.36031762_tile_1 SRC.chr20.36031762.36031762_tile_1 1 chr20 36031734 36031923 + CCAGCCCGGGGAGAACCTCTAGGCACAGGCGGGCCCAGACCGGCTTCTCGGCTTGGATCCTGGGCTGGGTGGCCCCTGTCTCGGGGCTTGCCCCACTCTGCCTGCCTGCTGTTGGTCCTCTCTCTGTGGGGCTGA Homo sapiens hg19 +GNAS1.chr20.57484420.57484421_tile_1 GNAS1.chr20.57484420.57484421_tile_1 1 chr20 57484390 57484560 + TGCCGTGTCCTGACTTCTGGAATCTTTGAGACCAAGTTCCAGGTGGACAAAGTCAACTTCCAGTAAGCCAACTGTTACCTTTTTATATAACAGAGATCATGGTTTCTTGACATTCAC Homo sapiens hg19 +SMARCB1_1.chr22.24133967.24133990_tile_1 SMARCB1_1.chr22.24133967.24133990_tile_1 1 chr22 24133939 24134126 + TCCGAGGTTCTCTGTACAAGAGATACCCCTCACTCTGGAGGCGACTAGCCACTGTGGAAGAGAGGAAGAAAATAGTTGCATCGTCACATGGTAAAAAAACAAAACCTAACACTAAGGGTGCGTCTTCACGAGGGTT Homo sapiens hg19 +SMARCB1_3.chr22.24143240.24143240_tile_1 SMARCB1_3.chr22.24143240.24143240_tile_1 1 chr22 24143210 24143383 + GGGCCGAGACAAGAAGAGAACCTTCCCCCTTTGGTGTGGATGCATCGCTGCACTCACCCTCCGTGCTGATTCCGCCTTAGTTCTCCAGCACGTTTCAGTTCCTTCCTCCCCAGAAAAACACT Homo sapiens hg19 +SMARCB1_4.chr22.24145582.24145582_tile_1 SMARCB1_4.chr22.24145582.24145582_tile_1 1 chr22 24145552 24145726 + GCTGCGAGACGCCTTCACCTGGAACATGAATGGTACAAGGCAGTCGGGCTTGGCTGGGCCTGGCCCCAACCCCTGTGTGTTACGTGGGAACAGTCCCGTTTCCTGCCAGCTGCCTGTCAGGC Homo sapiens hg19 +SMARCB1_5_6.chr22.24176352.24176357_tile_1 SMARCB1_5_6.chr22.24176352.24176357_tile_1 1 chr22 24176324 24176495 + CGGCCCCGGCCTGGTAACCAGCCCATCAGCACACGGCTCCCACGGAGCATCTCAGAAGATTGGGCCGCCTCTCCTCCATCTTCTGGCAAGGACAGAGGCGAGGGGACAGCCCAGCGCCA Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_1 GNA11_4.chr19.3114942.3115070_tile_1 1 chr19 3114824 3115004 - GTAGCCCAAGGTGGCGATGCGGTCAACGTCGGTCAGGTAGCTGCAACACAGCGGTGGGTGCTCAGGCCGGCTGCCGGGGGTGGGGGGGCAGGACAGGGACACAGCACCCAAACCAGCGGGAGGACGGAAAGCCACC Homo sapiens hg19 +GNA11_4.chr19.3114942.3115070_tile_2 GNA11_4.chr19.3114942.3115070_tile_2 1 chr19 3114958 3115133 + CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCATCATCGAGTACCCTTTCGACCTGGAGAACATCATCTTCCGGTACCGCCCGGGCCACAGCAGGCGGGGAGGGGGCACTGAGA Homo sapiens hg19 +GNA11_5.chr19.3118922.3119051_tile_1 GNA11_5.chr19.3118922.3119051_tile_1 1 chr19 3118802 3118989 - CACTTCCTCCGCTCCGACCGCTGGCCCCCCACATCCACCATCCTGAAAGGACACAGCGCCAGGACTCAGCCACCTGGCGCCCCAAGGCCCAATCTGCAATCCCAGGACGGCTCCCACCCAAGCCCCTCCTGCCACACC Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_6.chr19.3119204.3119357_tile_2 1 chr19 3119208 3119395 - CCGCAGCCCGGCGCACCATCGAACTCGGGGAAGTAGTCCACCAGGTGCGAGTACAGGATCTTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGAGGATGACGGAGGAGTTCTGGAACCAGGGGTAGGTGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_7.chr19.3120987.3121177_tile_1 1 chr19 3120865 3121035 + GGGCCTTACTCGCTCATCCCCTGGGAGTGACAAAGGGGCCCACGAGTCCCTTGCCCTGGGCCGGGCTGGGGCACAGCCTCACCCTCTGCCCTCCCCCAGGTCCCCAGCGGGACGCCCAGGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 1 chr19 3120985 3121170 - CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTCCGTGTCGGTGGCACACGTGAAGTGTGAGTAGATGATCTTGTCGCTGTCGGGGTTCAGGTCCACGAACATCTTCAGGATGAACTCCCGCGCCGC Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_3 GNA11_7.chr19.3120987.3121177_tile_3 1 chr19 3121121 3121304 + GCAGCTCAACCTCAAGGAGTACAACCTGGTCTGAGCGCCCAGGCCCAGGGAGACGGGATGGAGACACGGGGCAGGACCTTCCTTCCACGGAGCCTGCGGCTGCCGGGCGGGTGGCGCTGCCGAGTCCGGGCCGGGGC Homo sapiens hg19 +GNAQ_4.chr9.80412436.80412564_tile_1 GNAQ_4.chr9.80412436.80412564_tile_1 1 chr9 80412406 80412592 + TACCTGAAAATGACACTTTGTAAGTCAAAGGGGTATTCGATGATCCCTGTGGTGGGGACTCGAACTCTAAGCACATCTTGTTGCGTAGGCAGGTAGGCAGGGTCAGCTACGCGGTCCAAGTCATTAAGATAGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_5.chr9.80409379.80409508_tile_1 1 chr9 80409249 80409421 + AAAGAAGTAAGTTCACTCCATTCCCCACACCCTACTTTCTATCATTTACTTGTATCAGATAATAAAATGATAATCCATTGCCTGTCTAAAGAACACTTACCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 1 chr9 80409335 80409510 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCAAGTTCTCGTGGAGTCAGACAATGAGGTAAGTGTTCTTTA Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_3 GNAQ_5.chr9.80409379.80409508_tile_3 1 chr9 80409459 80409639 + TTTGGCCCCCTACATCGACCATTCTGCAAGGTTAACAATACTCATATTAATAACATATAAAGTAAAACTAAAAAGTCAACATAAATATAGCACTACTTACAAACTTAGGGAAAATATTCTCTTGAAT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_6.chr9.80343430.80343583_tile_1 1 chr9 80343306 80343476 + GGGCAGCAATGGTGCACTGTAGTGCGTTAACTCCCACACTGGGGTTTGGAGACAAAACCTATTCACAGCTACTGAGCTGTGGTATGAGTGCTGACTTACCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_2 GNAQ_6.chr9.80343430.80343583_tile_2 1 chr9 80343392 80343561 - GGTTCCAGAACTCCTCGGTTATTCTGTTCTTAAACAAGAAAGATCTTCTAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGTAAGTCAGCAC Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_3 GNAQ_6.chr9.80343430.80343583_tile_3 1 chr9 80343504 80343689 + CAGGGGTATGTGATAATTGTTCTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTGGAAAAAAAAAAAAAATCAGAAAAAACAAGGAGTGAATTACATGATTACTTAATTTGTGAATTGTGTTTATTTT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 1 chr9 80336110 80336280 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCAGGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAATTAGACCAGATTGTACT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_7.chr9.80336240.80336429_tile_2 1 chr9 80336204 80336374 - CTACTCCCACTTCACGTGCGCCACAGACACCGAGAATATCCGCTTTGTCTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGAGTACAATCTGGTCTAATTGTGCCTCC Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_3 GNAQ_7.chr9.80336240.80336429_tile_3 1 chr9 80336320 80336495 + GATAATTTTGTCACTGTCTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCTTTCGGCCAAGAGACAAGAGGGACACTTTGTTACCTA Homo sapiens hg19 +PIK3CA4_11.chr3.178936074.178936095_tile_1 PIK3CA4_11.chr3.178936074.178936095_tile_1 2 chr22 17052964 17053133 + ATCCTCTCTCTGAAATCACTGCGCAGGAGAAAGATTTTCTATGGACCACAGGTAAGTGCTAAAATGGAGATTCTCTGTTTCTTTTTCTTTATTACAGAAAAAATAACTGACTTTGG Homo sapiens hg19 +PIK3CA12.chr3.178938860.178938860_tile_1 PIK3CA12.chr3.178938860.178938860_tile_1 2 chr22 17055413 17055585 + CACCTGAATAGGCAAGTCGAGGCAATGGAAAAGCTCATTAACTTAACTGACATTGTCAAACAGGAGAAGAAGGATGAAACACAAAAGTTGTGTGACTCTAGTCTGTGTTTGAGACTCTT Homo sapiens hg19 +PTEN7.chr10.89717615.89717772_tile_1 PTEN3.chr10.89685307.89685307_tile_1 2 chr9 33675957 33676480 - ATACACAATCTTTGTGCTGAAAGACATTATGACACCGCCAAATCTAATTACAGAGTTGCGCAATATCCTTTTGAAGACCATAACCCACCACAGCTAGAACTTATCAAACCCTTTTGTGAAGATCTTGACCAATGGCTAAGTGAAGATGACAATCATGTTGCAGCAATTCACTGTAAAGCTGGAAAGGGACGAACTGGTATAATGATTTATGCATATTTATTACATCGGGGCAAATTTTTAAAGGCACAAGAGGCCCTAGATTTCTATGGGGAAGTAAGGACCAGAGACAAAAAGGGAGTAACTATTCCCAGTCAGAGGCGCTATGTGTATTACTATAGCTACCTGGTAAAGAATCATGTGGATTATAGACCAGTGGCACTGTTGTTTCACAAGATGATGTTTGAAACTATTCCAATGTTCAGTGGCGGAACTTGCAATCCTCAGTTTGTGGTCTGCCAGCTAAAG Homo sapiens hg19 +PTEN13.chr10.89720716.89720852_tile_1 PTEN13.chr10.89720716.89720852_tile_1 2 chr9 33675629 33675815 - CAGAAAAAGTAGAAAATGGAAGTCTATGTGATCAAGAAATTGATAGCATTTGCAGTATAGAGCGTGCAGATAATGACAAGGAGTATCTAGTACTTACTTTAACAAAAAATGATCTTGACAAAGCAAATAAAGACA Homo sapiens hg19 +GNA11_6.chr19.3119204.3119357_tile_2 GNA11_7.chr19.3120987.3121177_tile_2 2 chr7 65970150 65970483 + CAGGATGGTGTCCTTCACGGCCGCGAACACGAAGCGGATGTTCTTCGTGTCGGTGGCGTACGTGAAGTGGGAGTCGATGATCTTGTCGCTGTCGGGGTTCATGTCCACTAACATCTTCAGGATGAACTCCCGCGCCGCCTGGGCGTCCTGCTGGGGCCCTTCGAACTCGGGGAAGTAGTCCACCATGTGTGAGTACAGGATATTGTCCTCCAGCAGGTCCTTCTTGTTGAGGAAGGTGATGACGGGGGAGTTCTGGAACCAGGGGTAGTCGATGATGGTCCGG Homo sapiens hg19 +GNA11_7.chr19.3120987.3121177_tile_1 GNA11_4.chr19.3114942.3115070_tile_2 2 chr7 65970285 65970719 - CCTGCCCACCCAGCAGGACGTGCTGCGGGTCCGCGTGCCCACCACCGGCGTCTTTCGACCTGGAGAACATCATCTTCAGGATGGCGGATGTTGGGGGACAGCGGTCGGCGCAGAGGAAGTGGATCCACTGCTTTGAGAACCTGACGTCCATCCCGTTTCTCGTCGCCCTCAGTGAATACGACCAAGTCCTGGTGGAGTCGGACAACGAGAACCGGATGGAGGAGAGCAAAGCCCTGTTCCGGACCATCATCGACTACCCCTGGTTCCAGAACTCCCCCGTCATCACCTTCCTCAACAAGAAGGACCTGCTGGAGGACAATATCCTGTACTCACACATGGTGGACTACTTCCCCGAGTTCGAAGGGCCCCAGCAGGACGCCCAGGC Homo sapiens hg19 +GNAQ_5.chr9.80409379.80409508_tile_1 GNAQ_7.chr9.80336240.80336429_tile_1 2 chr2 132181238 132181750 + TTAGTATTATGCAAATTGTTTTCCACAGAAATACAGTCCCTCTTGTGTATCTTCAATAGCCCACCATGGAAGGGCAGGGCGGGTGTCTAGGAGGCACAACTAGACCAGATTGTAATCCTTCAGGTTCAACTGGAGGATGGTGTCCTTGACGGCAGCAAACACAAAGCGGATATTCTCGGTGTCTGTGGCGCATGTGAAGTGGGAGTAGATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGTAGTCGACTAGATGGGAATACATGATTTTCTCCTCTGGAAGATCTTTCTTGTTTAACAACAGAATAACCGAGGAGTTCTGGAACCAGGGATACGTGATAATTGTACTAAAGAGAGCCTTGCTTTCCTCCATTCGGTTCTCATTGTCTGACT Homo sapiens hg19 +GNAQ_6.chr9.80343430.80343583_tile_1 GNAQ_7.chr9.80336240.80336429_tile_3 2 chr2 132181448 132181600 + GATAATTTGGTCACTGGGTTCAGGTCCACGAACATCTTCAGAATGAATTCTCGGGCTGCCTGGGCATCTCTCTGGGGTCCATCATATTCTGGGAAGT Homo sapiens hg19 +GNAQ_7.chr9.80336240.80336429_tile_2 GNAQ_5.chr9.80409379.80409508_tile_2 2 chr2 132181332 132181839 - AGGTCAGAGAGAAGAAAATGGATACACTGCTTTGAAAATGTCACCTCTATCATGTTTCTAGTAGCGCTTAGTGAATATGATCGAGTTCTCGTGGAGTCAGACAATGAGAACCGAATGGAGGAAAGCAAGGCTCTCTTTAGTACAATTATCACGTATCCCTGGTTCCAGAACTCCTCGGTTATTCTGTTGTTAAACAAGAAAGATCTTCCAGAGGAGAAAATCATGTATTCCCATCTAGTCGACTACTTCCCAGAATATGATGGACCCCAGAGAGATGCCCAGGCAGCCCGAGAATTCATTCTGAAGATGTTCGTGGACCTGAACCCAGTGACCAAATTATCTACTCCCACTTCACATGCGCCACAGACACCGAGAATATCCGCTTTGTGTTTGCTGCCGTCAAGGACACCATCCTCCAGTTGAACCTGAAGGATTACAATCTGGTCTAGTTGTGCCTCC Homo sapiens hg19
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool-data/all_fasta.loc.sample Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,26 @@ +#This is a sample file distributed with Galaxy that enables tools +#to use a directory with indexed fasta files. The all_fasta.loc file has +#this format (longer white space characters are TAB characters): +# +#<unique_build_id> <dbkey> <display_name> <file_path> +# +#So, for example, if you had phiX indexed stored in +#/example/path/ +#then the all_fasta.loc entry would look like this: +# +#phiX174 phiX phiX Pretty /example/path/phiX.fa +# +#and your /example/path/ directory +#would contain phiX.fa.* files: +# +# phiX.fa.fai +# phiX.fa.dict +# +#Your all_fasta.loc file should include an entry per line for each +#index set you have stored. For example: +# +#phiX174 phiX phiX174 /path/to/phiX.fa +#hg18 hg18 hg18 Full /path/to/hg18full.fa +#hg19 hg19 hg19 /path/to/hg19.fa +#...etc... +#
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool_data_table_conf.xml.sample Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,6 @@ +<tables> + <table name="all_fasta" comment_char="#"> + <columns>value, dbkey, name, path</columns> + <file path="tool-data/all_fasta.loc" /> + </table> +</tables>
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool_dependencies.xml Fri Mar 20 08:58:17 2015 -0400 @@ -0,0 +1,12 @@ +<?xml version="1.0"?> +<tool_dependency> + + <package name="R" version="3.0.1"> + <repository changeset_revision="349e070fdac8" name="package_r_3_0_1" owner="iuc" prior_installation_required="TRUE" toolshed="https://testtoolshed.g2.bx.psu.edu" /> + </package> + + <package name="samtools" version="0.1.19"> + <repository changeset_revision="786e3000ca58" name="package_samtools_0_1_19" owner="devteam" prior_installation_required="TRUE" toolshed="https://testtoolshed.g2.bx.psu.edu" /> + </package> + +</tool_dependency>