##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
