diff test-data/ERR2510682.results.json @ 0:5b218b5eedb6 draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/main/tools/tb-profiler commit 7dba70c70c9fe33353a0fd21803b11cfddc42c32
author iuc
date Tue, 21 Oct 2025 10:24:27 +0000
parents
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--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/ERR2510682.results.json	Tue Oct 21 10:24:27 2025 +0000
@@ -0,0 +1,10292 @@
+{
+    "schema_version": "1.0.0",
+    "id": "ERR2510682",
+    "timestamp": "2025-08-14T09:13:09.391314",
+    "pipeline": {
+        "software_version": "6.6.4",
+        "db_version": {
+            "name": "tbdb",
+            "repo": "git@github.com:jodyphelan/tbdb.git",
+            "branch": "tbdb",
+            "commit": "3ed1cb99",
+            "status": "clean",
+            "author": "Jody Phelan",
+            "date": "Sun Feb 16 11:08:45 2025 +0100",
+            "db-schema-version": "2.0.0",
+            "tb-profiler-version": ">=6.6.0,<7.0.0"
+        },
+        "software": [
+            {
+                "process": "variant_calling",
+                "software": "freebayes",
+                "version": "1.3.6"
+            },
+            {
+                "process": "long_variant_calling",
+                "software": "delly",
+                "version": "1.3.3"
+            },
+            {
+                "process": "depth_calculation",
+                "software": "samtools",
+                "version": "1.22"
+            }
+        ]
+    },
+    "notes": [],
+    "lineage": [
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+    ],
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+    "drtype": "Pre-XDR-TB",
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+        {
+            "chrom": "Chromosome",
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+                {
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+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Ser91Pro",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0006",
+                    "gene_name": "gyrA",
+                    "feature_id": "Rv0006",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.271T>C",
+                    "protein_change": "p.Ser91Pro",
+                    "sequence_hgvs": "Chromosome:g.7572T>C",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "levofloxacin",
+                            "original_mutation": "p.Ser91Pro",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "drug_resistance",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "p.Ser91Pro",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": "Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Ser91Pro",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Ser91Pro",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                }
+            ],
+            "locus_tag": "Rv0006",
+            "gene_associated_drugs": [
+                "levofloxacin",
+                "moxifloxacin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 7582,
+            "ref": "A",
+            "alt": "G",
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+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 7,
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+            "sv_len": null,
+            "gene_id": "Rv0006",
+            "gene_name": "gyrA",
+            "feature_id": "Rv0006",
+            "type": "missense_variant",
+            "change": "p.Asp94Gly",
+            "nucleotide_change": "c.281A>G",
+            "protein_change": "p.Asp94Gly",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Asp94Gly",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Asp94Gly",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "High-level resistance"
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0006",
+                    "gene_name": "gyrA",
+                    "feature_id": "Rv0006",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.281A>G",
+                    "protein_change": "p.Asp94Gly",
+                    "sequence_hgvs": "Chromosome:g.7582A>G",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "levofloxacin",
+                            "original_mutation": "p.Asp94Gly",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "drug_resistance",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "p.Asp94Gly",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": "High-level resistance"
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Asp94Gly",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Asp94Gly",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "High-level resistance"
+                }
+            ],
+            "locus_tag": "Rv0006",
+            "gene_associated_drugs": [
+                "levofloxacin",
+                "moxifloxacin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 761155,
+            "ref": "C",
+            "alt": "T",
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+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 15,
+            "reverse_reads": 14,
+            "sv_len": null,
+            "gene_id": "Rv0667",
+            "gene_name": "rpoB",
+            "feature_id": "Rv0667",
+            "type": "missense_variant",
+            "change": "p.Ser450Leu",
+            "nucleotide_change": "c.1349C>T",
+            "protein_change": "p.Ser450Leu",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Ser450Leu",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0667",
+                    "gene_name": "rpoB",
+                    "feature_id": "Rv0667",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1349C>T",
+                    "protein_change": "p.Ser450Leu",
+                    "sequence_hgvs": "Chromosome:g.761155C>T",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "rifampicin",
+                            "original_mutation": "RRDR non-silent",
+                            "confidence": "Assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": "Expert rule: Non-silent variants in RRDR of rpoB"
+                        },
+                        {
+                            "type": "drug_resistance",
+                            "drug": "rifampicin",
+                            "original_mutation": "p.Ser450Leu",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Ser450Leu",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "locus_tag": "Rv0667",
+            "gene_associated_drugs": [
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 781822,
+            "ref": "A",
+            "alt": "G",
+            "depth": 52,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 24,
+            "reverse_reads": 28,
+            "sv_len": null,
+            "gene_id": "Rv0682",
+            "gene_name": "rpsL",
+            "feature_id": "Rv0682",
+            "type": "missense_variant",
+            "change": "p.Lys88Arg",
+            "nucleotide_change": "c.263A>G",
+            "protein_change": "p.Lys88Arg",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "streptomycin",
+                    "original_mutation": "p.Lys88Arg",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0682",
+                    "gene_name": "rpsL",
+                    "feature_id": "Rv0682",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.263A>G",
+                    "protein_change": "p.Lys88Arg",
+                    "sequence_hgvs": "Chromosome:g.781822A>G",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "streptomycin",
+                            "original_mutation": "p.Lys88Arg",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "streptomycin",
+                    "original_mutation": "p.Lys88Arg",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "locus_tag": "Rv0682",
+            "gene_associated_drugs": [
+                "streptomycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 1673425,
+            "ref": "C",
+            "alt": "T",
+            "depth": 49,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 20,
+            "reverse_reads": 29,
+            "sv_len": null,
+            "gene_id": "Rv1484",
+            "gene_name": "inhA",
+            "feature_id": "Rv1484",
+            "type": "upstream_gene_variant",
+            "change": "c.-777C>T",
+            "nucleotide_change": "c.-777C>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethionamide",
+                    "original_mutation": "c.-777C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Alias fabG1_c.-15C>T"
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "isoniazid",
+                    "original_mutation": "c.-777C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Alias fabG1_c.-15C>T. Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1484",
+                    "gene_name": "inhA",
+                    "feature_id": "Rv1484",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-777C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1673425C>T",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "ethionamide",
+                            "original_mutation": "c.-777C>T",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": "Alias fabG1_c.-15C>T"
+                        },
+                        {
+                            "type": "drug_resistance",
+                            "drug": "isoniazid",
+                            "original_mutation": "c.-777C>T",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": "Alias fabG1_c.-15C>T. Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethionamide",
+                    "original_mutation": "c.-777C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Alias fabG1_c.-15C>T"
+                },
+                {
+                    "type": "drug_resistance",
+                    "drug": "isoniazid",
+                    "original_mutation": "c.-777C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "Alias fabG1_c.-15C>T. Low-level resistance (multiple, genetically linked low-level resistance mutations are additive and confer high-level resistance)"
+                }
+            ],
+            "locus_tag": "Rv1484",
+            "gene_associated_drugs": [
+                "ethionamide",
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 2155168,
+            "ref": "C",
+            "alt": "G",
+            "depth": 23,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 12,
+            "reverse_reads": 11,
+            "sv_len": null,
+            "gene_id": "Rv1908c",
+            "gene_name": "katG",
+            "feature_id": "Rv1908c",
+            "type": "missense_variant",
+            "change": "p.Ser315Thr",
+            "nucleotide_change": "c.944G>C",
+            "protein_change": "p.Ser315Thr",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "isoniazid",
+                    "original_mutation": "p.Ser315Thr",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "High-level resistance"
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1908c",
+                    "gene_name": "katG",
+                    "feature_id": "Rv1908c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.944G>C",
+                    "protein_change": "p.Ser315Thr",
+                    "sequence_hgvs": "Chromosome:g.2155168C>G",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "isoniazid",
+                            "original_mutation": "p.Ser315Thr",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": "High-level resistance"
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "isoniazid",
+                    "original_mutation": "p.Ser315Thr",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": "High-level resistance"
+                }
+            ],
+            "locus_tag": "Rv1908c",
+            "gene_associated_drugs": [
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 2289252,
+            "ref": "T",
+            "alt": "C",
+            "depth": 33,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 17,
+            "reverse_reads": 16,
+            "sv_len": null,
+            "gene_id": "Rv2043c",
+            "gene_name": "pncA",
+            "feature_id": "Rv2043c",
+            "type": "upstream_gene_variant",
+            "change": "c.-11A>G",
+            "nucleotide_change": "c.-11A>G",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "c.-11A>G",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv2043c",
+                    "gene_name": "pncA",
+                    "feature_id": "Rv2043c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-11A>G",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.2289252T>C",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.-11A>G",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "c.-11A>G",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "locus_tag": "Rv2043c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 2715344,
+            "ref": "G",
+            "alt": "A",
+            "depth": 49,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 26,
+            "reverse_reads": 23,
+            "sv_len": null,
+            "gene_id": "Rv2416c",
+            "gene_name": "eis",
+            "feature_id": "Rv2416c",
+            "type": "upstream_gene_variant",
+            "change": "c.-12C>T",
+            "nucleotide_change": "c.-12C>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "kanamycin",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv2416c",
+                    "gene_name": "eis",
+                    "feature_id": "Rv2416c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-12C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.2715344G>A",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "kanamycin",
+                            "original_mutation": "c.-12C>T",
+                            "confidence": "Assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "c.-12C>T",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "kanamycin",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "locus_tag": "Rv2416c",
+            "gene_associated_drugs": [
+                "amikacin",
+                "kanamycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4243221,
+            "ref": "C",
+            "alt": "T",
+            "depth": 45,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 20,
+            "reverse_reads": 25,
+            "sv_len": null,
+            "gene_id": "Rv3794",
+            "gene_name": "embA",
+            "feature_id": "Rv3794",
+            "type": "upstream_gene_variant",
+            "change": "c.-12C>T",
+            "nucleotide_change": "c.-12C>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethambutol",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "tbdb",
+                    "comment": "Mutation from literature: doi: 10.1128/AAC.03285-14"
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "ethambutol",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3794",
+                    "gene_name": "embA",
+                    "feature_id": "Rv3794",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-12C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.4243221C>T",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "ethambutol",
+                            "original_mutation": "c.-12C>T",
+                            "confidence": "Uncertain significance",
+                            "source": "tbdb",
+                            "comment": "Mutation from literature: doi: 10.1128/AAC.03285-14"
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethambutol",
+                            "original_mutation": "c.-12C>T",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethambutol",
+                    "original_mutation": "c.-12C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "tbdb",
+                    "comment": "Mutation from literature: doi: 10.1128/AAC.03285-14"
+                }
+            ],
+            "locus_tag": "Rv3794",
+            "gene_associated_drugs": [
+                "ethambutol"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4247513,
+            "ref": "T",
+            "alt": "C",
+            "depth": 45,
+            "freq": 0.9111111111111111,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 18,
+            "reverse_reads": 23,
+            "sv_len": null,
+            "gene_id": "Rv3795",
+            "gene_name": "embB",
+            "feature_id": "Rv3795",
+            "type": "missense_variant",
+            "change": "p.Tyr334His",
+            "nucleotide_change": "c.1000T>C",
+            "protein_change": "p.Tyr334His",
+            "annotation": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethambutol",
+                    "original_mutation": "p.Tyr334His",
+                    "confidence": "Uncertain significance",
+                    "source": "tbdb",
+                    "comment": "Mutation from literature"
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "ethambutol",
+                    "original_mutation": "p.Tyr334His",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3795",
+                    "gene_name": "embB",
+                    "feature_id": "Rv3795",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1000T>C",
+                    "protein_change": "p.Tyr334His",
+                    "sequence_hgvs": "Chromosome:g.4247513T>C",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "ethambutol",
+                            "original_mutation": "p.Tyr334His",
+                            "confidence": "Uncertain significance",
+                            "source": "tbdb",
+                            "comment": "Mutation from literature"
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethambutol",
+                            "original_mutation": "p.Tyr334His",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "drugs": [
+                {
+                    "type": "drug_resistance",
+                    "drug": "ethambutol",
+                    "original_mutation": "p.Tyr334His",
+                    "confidence": "Uncertain significance",
+                    "source": "tbdb",
+                    "comment": "Mutation from literature"
+                }
+            ],
+            "locus_tag": "Rv3795",
+            "gene_associated_drugs": [
+                "ethambutol"
+            ]
+        }
+    ],
+    "other_variants": [
+        {
+            "chrom": "Chromosome",
+            "pos": 7362,
+            "ref": "G",
+            "alt": "C",
+            "depth": 63,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 29,
+            "reverse_reads": 34,
+            "sv_len": null,
+            "gene_id": "Rv0006",
+            "gene_name": "gyrA",
+            "feature_id": "Rv0006",
+            "type": "missense_variant",
+            "change": "p.Glu21Gln",
+            "nucleotide_change": "c.61G>C",
+            "protein_change": "p.Glu21Gln",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Glu21Gln",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Glu21Gln",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0006",
+                    "gene_name": "gyrA",
+                    "feature_id": "Rv0006",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.61G>C",
+                    "protein_change": "p.Glu21Gln",
+                    "sequence_hgvs": "Chromosome:g.7362G>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "levofloxacin",
+                            "original_mutation": "p.Glu21Gln",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "p.Glu21Gln",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0006",
+            "gene_associated_drugs": [
+                "levofloxacin",
+                "moxifloxacin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 7585,
+            "ref": "G",
+            "alt": "C",
+            "depth": 27,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 12,
+            "reverse_reads": 15,
+            "sv_len": null,
+            "gene_id": "Rv0006",
+            "gene_name": "gyrA",
+            "feature_id": "Rv0006",
+            "type": "missense_variant",
+            "change": "p.Ser95Thr",
+            "nucleotide_change": "c.284G>C",
+            "protein_change": "p.Ser95Thr",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Ser95Thr",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Ser95Thr",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0006",
+                    "gene_name": "gyrA",
+                    "feature_id": "Rv0006",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.284G>C",
+                    "protein_change": "p.Ser95Thr",
+                    "sequence_hgvs": "Chromosome:g.7585G>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "levofloxacin",
+                            "original_mutation": "p.Ser95Thr",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "p.Ser95Thr",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0006",
+            "gene_associated_drugs": [
+                "levofloxacin",
+                "moxifloxacin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 9304,
+            "ref": "G",
+            "alt": "A",
+            "depth": 38,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 18,
+            "reverse_reads": 20,
+            "sv_len": null,
+            "gene_id": "Rv0006",
+            "gene_name": "gyrA",
+            "feature_id": "Rv0006",
+            "type": "missense_variant",
+            "change": "p.Gly668Asp",
+            "nucleotide_change": "c.2003G>A",
+            "protein_change": "p.Gly668Asp",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "levofloxacin",
+                    "original_mutation": "p.Gly668Asp",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "p.Gly668Asp",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0006",
+                    "gene_name": "gyrA",
+                    "feature_id": "Rv0006",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.2003G>A",
+                    "protein_change": "p.Gly668Asp",
+                    "sequence_hgvs": "Chromosome:g.9304G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "levofloxacin",
+                            "original_mutation": "p.Gly668Asp",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "p.Gly668Asp",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0006",
+            "gene_associated_drugs": [
+                "levofloxacin",
+                "moxifloxacin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 491742,
+            "ref": "T",
+            "alt": "C",
+            "depth": 48,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 30,
+            "reverse_reads": 18,
+            "sv_len": null,
+            "gene_id": "Rv0407",
+            "gene_name": "fgd1",
+            "feature_id": "Rv0407",
+            "type": "synonymous_variant",
+            "change": "c.960T>C",
+            "nucleotide_change": "c.960T>C",
+            "protein_change": "p.Phe320Phe",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "original_mutation": "c.960T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "delamanid",
+                    "original_mutation": "c.960T>C",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "pretomanid",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0407",
+                    "gene_name": "fgd1",
+                    "feature_id": "Rv0407",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.960T>C",
+                    "protein_change": "p.Phe320Phe",
+                    "sequence_hgvs": "Chromosome:g.491742T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "c.960T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "delamanid",
+                            "original_mutation": "c.960T>C",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0407",
+            "gene_associated_drugs": [
+                "clofazimine",
+                "delamanid",
+                "pretomanid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 575907,
+            "ref": "C",
+            "alt": "T",
+            "depth": 42,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
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+            "reverse_reads": 20,
+            "sv_len": null,
+            "gene_id": "Rv0486",
+            "gene_name": "mshA",
+            "feature_id": "Rv0486",
+            "type": "missense_variant",
+            "change": "p.Ala187Val",
+            "nucleotide_change": "c.560C>T",
+            "protein_change": "p.Ala187Val",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethionamide",
+                    "original_mutation": "p.Ala187Val",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "original_mutation": "p.Ala187Val",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0486",
+                    "gene_name": "mshA",
+                    "feature_id": "Rv0486",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.560C>T",
+                    "protein_change": "p.Ala187Val",
+                    "sequence_hgvs": "Chromosome:g.575907C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethionamide",
+                            "original_mutation": "p.Ala187Val",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "p.Ala187Val",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0486",
+            "gene_associated_drugs": [
+                "ethionamide",
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 620625,
+            "ref": "A",
+            "alt": "G",
+            "depth": 44,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 26,
+            "reverse_reads": 18,
+            "sv_len": null,
+            "gene_id": "Rv0529",
+            "gene_name": "ccsA",
+            "feature_id": "Rv0529",
+            "type": "missense_variant",
+            "change": "p.Ile245Met",
+            "nucleotide_change": "c.735A>G",
+            "protein_change": "p.Ile245Met",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "p.Ile245Met",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "p.Ile245Met",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "p.Ile245Met",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0529",
+                    "gene_name": "ccsA",
+                    "feature_id": "Rv0529",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.735A>G",
+                    "protein_change": "p.Ile245Met",
+                    "sequence_hgvs": "Chromosome:g.620625A>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "p.Ile245Met",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "p.Ile245Met",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "p.Ile245Met",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0529",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 657081,
+            "ref": "C",
+            "alt": "T",
+            "depth": 50,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 28,
+            "reverse_reads": 22,
+            "sv_len": null,
+            "gene_id": "Rv0565c",
+            "gene_name": "Rv0565c",
+            "feature_id": "Rv0565c",
+            "type": "synonymous_variant",
+            "change": "c.390G>A",
+            "nucleotide_change": "c.390G>A",
+            "protein_change": "p.Val130Val",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethionamide",
+                    "original_mutation": "c.390G>A",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0565c",
+                    "gene_name": "Rv0565c",
+                    "feature_id": "Rv0565c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.390G>A",
+                    "protein_change": "p.Val130Val",
+                    "sequence_hgvs": "Chromosome:g.657081C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethionamide",
+                            "original_mutation": "c.390G>A",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0565c",
+            "gene_associated_drugs": [
+                "ethionamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 657142,
+            "ref": "C",
+            "alt": "T",
+            "depth": 72,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 36,
+            "reverse_reads": 36,
+            "sv_len": null,
+            "gene_id": "Rv0565c",
+            "gene_name": "Rv0565c",
+            "feature_id": "Rv0565c",
+            "type": "missense_variant",
+            "change": "p.Arg110His",
+            "nucleotide_change": "c.329G>A",
+            "protein_change": "p.Arg110His",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethionamide",
+                    "original_mutation": "p.Arg110His",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0565c",
+                    "gene_name": "Rv0565c",
+                    "feature_id": "Rv0565c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.329G>A",
+                    "protein_change": "p.Arg110His",
+                    "sequence_hgvs": "Chromosome:g.657142C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethionamide",
+                            "original_mutation": "p.Arg110His",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0565c",
+            "gene_associated_drugs": [
+                "ethionamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 737293,
+            "ref": "CA",
+            "alt": "AC",
+            "depth": 96,
+            "freq": 0.11458333333333333,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 7,
+            "reverse_reads": 4,
+            "sv_len": null,
+            "gene_id": "Rv0643c",
+            "gene_name": "mmaA3",
+            "feature_id": "Rv0643c",
+            "type": "missense_variant",
+            "change": "p.Cys286Val",
+            "nucleotide_change": "c.856_857delTGinsGT",
+            "protein_change": "p.Cys286Val",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0643c",
+                    "gene_name": "mmaA3",
+                    "feature_id": "Rv0643c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.856_857delTGinsGT",
+                    "protein_change": "p.Cys286Val",
+                    "sequence_hgvs": "Chromosome:g.737293CA>AC",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0643c",
+            "gene_associated_drugs": [
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 738040,
+            "ref": "C",
+            "alt": "T",
+            "depth": 100,
+            "freq": 0.21,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 8,
+            "reverse_reads": 13,
+            "sv_len": null,
+            "gene_id": "Rv0643c",
+            "gene_name": "mmaA3",
+            "feature_id": "Rv0643c",
+            "type": "missense_variant",
+            "change": "p.Arg37Gln",
+            "nucleotide_change": "c.110G>A",
+            "protein_change": "p.Arg37Gln",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0643c",
+                    "gene_name": "mmaA3",
+                    "feature_id": "Rv0643c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.110G>A",
+                    "protein_change": "p.Arg37Gln",
+                    "sequence_hgvs": "Chromosome:g.738040C>T",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0643c",
+            "gene_associated_drugs": [
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 763031,
+            "ref": "T",
+            "alt": "C",
+            "depth": 28,
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+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 14,
+            "reverse_reads": 13,
+            "sv_len": null,
+            "gene_id": "Rv0667",
+            "gene_name": "rpoB",
+            "feature_id": "Rv0667",
+            "type": "synonymous_variant",
+            "change": "c.3225T>C",
+            "nucleotide_change": "c.3225T>C",
+            "protein_change": "p.Ala1075Ala",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "c.3225T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0667",
+                    "gene_name": "rpoB",
+                    "feature_id": "Rv0667",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.3225T>C",
+                    "protein_change": "p.Ala1075Ala",
+                    "sequence_hgvs": "Chromosome:g.763031T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "c.3225T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                },
+                {
+                    "gene_id": "Rv0668",
+                    "gene_name": "rpoC",
+                    "feature_id": "Rv0668",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-339T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.763031T>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0667",
+            "gene_associated_drugs": [
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 764817,
+            "ref": "T",
+            "alt": "G",
+            "depth": 54,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 26,
+            "reverse_reads": 28,
+            "sv_len": null,
+            "gene_id": "Rv0668",
+            "gene_name": "rpoC",
+            "feature_id": "Rv0668",
+            "type": "missense_variant",
+            "change": "p.Val483Gly",
+            "nucleotide_change": "c.1448T>G",
+            "protein_change": "p.Val483Gly",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Val483Gly",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0668",
+                    "gene_name": "rpoC",
+                    "feature_id": "Rv0668",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1448T>G",
+                    "protein_change": "p.Val483Gly",
+                    "sequence_hgvs": "Chromosome:g.764817T>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "p.Val483Gly",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0668",
+            "gene_associated_drugs": [
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 766645,
+            "ref": "A",
+            "alt": "C",
+            "depth": 40,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 20,
+            "reverse_reads": 20,
+            "sv_len": null,
+            "gene_id": "Rv0668",
+            "gene_name": "rpoC",
+            "feature_id": "Rv0668",
+            "type": "missense_variant",
+            "change": "p.Glu1092Asp",
+            "nucleotide_change": "c.3276A>C",
+            "protein_change": "p.Glu1092Asp",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Glu1092Asp",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0668",
+                    "gene_name": "rpoC",
+                    "feature_id": "Rv0668",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.3276A>C",
+                    "protein_change": "p.Glu1092Asp",
+                    "sequence_hgvs": "Chromosome:g.766645A>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "p.Glu1092Asp",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0668",
+            "gene_associated_drugs": [
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 775639,
+            "ref": "T",
+            "alt": "C",
+            "depth": 12,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 7,
+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "missense_variant",
+            "change": "p.Ile948Val",
+            "nucleotide_change": "c.2842A>G",
+            "protein_change": "p.Ile948Val",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.Ile948Val",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "original_mutation": "p.Ile948Val",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.2842A>G",
+                    "protein_change": "p.Ile948Val",
+                    "sequence_hgvs": "Chromosome:g.775639T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.Ile948Val",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "p.Ile948Val",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 776100,
+            "ref": "G",
+            "alt": "A",
+            "depth": 37,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 15,
+            "reverse_reads": 22,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "missense_variant",
+            "change": "p.Thr794Ile",
+            "nucleotide_change": "c.2381C>T",
+            "protein_change": "p.Thr794Ile",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.Thr794Ile",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "original_mutation": "p.Thr794Ile",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.2381C>T",
+                    "protein_change": "p.Thr794Ile",
+                    "sequence_hgvs": "Chromosome:g.776100G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.Thr794Ile",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "p.Thr794Ile",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 776182,
+            "ref": "C",
+            "alt": "T",
+            "depth": 44,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 20,
+            "reverse_reads": 24,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "missense_variant",
+            "change": "p.Asp767Asn",
+            "nucleotide_change": "c.2299G>A",
+            "protein_change": "p.Asp767Asn",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.Asp767Asn",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "original_mutation": "p.Asp767Asn",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.2299G>A",
+                    "protein_change": "p.Asp767Asn",
+                    "sequence_hgvs": "Chromosome:g.776182C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.Asp767Asn",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "p.Asp767Asn",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 777128,
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+            "alt": "C",
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+            "freq": 0.1323529411764706,
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+            "filter": "pass",
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+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "synonymous_variant",
+            "change": "c.1353A>G",
+            "nucleotide_change": "c.1353A>G",
+            "protein_change": "p.Glu451Glu",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.1353A>G",
+                    "protein_change": "p.Glu451Glu",
+                    "sequence_hgvs": "Chromosome:g.777128T>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 779615,
+            "ref": "G",
+            "alt": "C",
+            "depth": 53,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
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+            "reverse_reads": 29,
+            "sv_len": null,
+            "gene_id": "Rv0677c",
+            "gene_name": "mmpS5",
+            "feature_id": "Rv0677c",
+            "type": "upstream_gene_variant",
+            "change": "c.-710C>G",
+            "nucleotide_change": "c.-710C>G",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0677c",
+                    "gene_name": "mmpS5",
+                    "feature_id": "Rv0677c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-710C>G",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.779615G>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0677c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 781395,
+            "ref": "T",
+            "alt": "C",
+            "depth": 39,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 17,
+            "reverse_reads": 22,
+            "sv_len": null,
+            "gene_id": "Rv0682",
+            "gene_name": "rpsL",
+            "feature_id": "Rv0682",
+            "type": "upstream_gene_variant",
+            "change": "c.-165T>C",
+            "nucleotide_change": "c.-165T>C",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "c.-165T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0682",
+                    "gene_name": "rpsL",
+                    "feature_id": "Rv0682",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-165T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.781395T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "c.-165T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0682",
+            "gene_associated_drugs": [
+                "streptomycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 1254562,
+            "ref": "A",
+            "alt": "G",
+            "depth": 94,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 39,
+            "reverse_reads": 55,
+            "sv_len": null,
+            "gene_id": "Rv1129c",
+            "gene_name": "Rv1129c",
+            "feature_id": "Rv1129c",
+            "type": "upstream_gene_variant",
+            "change": "c.-28T>C",
+            "nucleotide_change": "c.-28T>C",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "original_mutation": "c.-28T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "levofloxacin",
+                    "original_mutation": "c.-28T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "moxifloxacin",
+                    "original_mutation": "c.-28T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "c.-28T>C",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1129c",
+                    "gene_name": "Rv1129c",
+                    "feature_id": "Rv1129c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-28T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1254562A>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "c.-28T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "levofloxacin",
+                            "original_mutation": "c.-28T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "moxifloxacin",
+                            "original_mutation": "c.-28T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "c.-28T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv1129c",
+            "gene_associated_drugs": [
+                "isoniazid",
+                "levofloxacin",
+                "moxifloxacin",
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 1364706,
+            "ref": "G",
+            "alt": "A",
+            "depth": 38,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 17,
+            "reverse_reads": 21,
+            "sv_len": null,
+            "gene_id": "Rv1221",
+            "gene_name": "sigE",
+            "feature_id": "Rv1221",
+            "type": "synonymous_variant",
+            "change": "c.294G>A",
+            "nucleotide_change": "c.294G>A",
+            "protein_change": "p.Leu98Leu",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "c.294G>A",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1221",
+                    "gene_name": "sigE",
+                    "feature_id": "Rv1221",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.294G>A",
+                    "protein_change": "p.Leu98Leu",
+                    "sequence_hgvs": "Chromosome:g.1364706G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.294G>A",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv1221",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 1406760,
+            "ref": "T",
+            "alt": "TG",
+            "depth": 29,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 15,
+            "reverse_reads": 14,
+            "sv_len": null,
+            "gene_id": "Rv1258c",
+            "gene_name": "Rv1258c",
+            "feature_id": "Rv1258c",
+            "type": "frameshift_variant",
+            "change": "c.580_581insC",
+            "nucleotide_change": "c.580_581insC",
+            "protein_change": "p.Glu194fs",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "original_mutation": "LoF",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "LoF",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "LoF",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1258c",
+                    "gene_name": "Rv1258c",
+                    "feature_id": "Rv1258c",
+                    "type": "frameshift_variant",
+                    "nucleotide_change": "c.580_581insC",
+                    "protein_change": "p.Glu194fs",
+                    "sequence_hgvs": "Chromosome:g.1406760T>TG",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "LoF",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "p.Glu194fs",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "LoF",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "p.Glu194fs",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "LoF",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "p.Glu194fs",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv1258c",
+            "gene_associated_drugs": [
+                "isoniazid",
+                "pyrazinamide",
+                "streptomycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "depth": 76,
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+            "gene_id": "EBG00000313325",
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+            "feature_id": "EBG00000313325",
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+            "change": "n.-187C>T",
+            "nucleotide_change": "n.-187C>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "EBG00000313325",
+                    "gene_name": "rrs",
+                    "feature_id": "EBG00000313325",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "n.-187C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1471659C>T",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "EBG00000313325",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin",
+                "streptomycin"
+            ]
+        },
+        {
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+            "alt": "A",
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+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "EBG00000313325",
+            "gene_name": "rrs",
+            "feature_id": "EBG00000313325",
+            "type": "non_coding_transcript_exon_variant",
+            "change": "n.699C>A",
+            "nucleotide_change": "n.699C>A",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "n.699C>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "n.699C>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "n.699C>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "EBG00000313325",
+                    "gene_name": "rrs",
+                    "feature_id": "EBG00000313325",
+                    "type": "non_coding_transcript_exon_variant",
+                    "nucleotide_change": "n.699C>A",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1472544C>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "n.699C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.699C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "n.699C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "n.699C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "EBG00000313325",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin",
+                "streptomycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "depth": 49,
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+            "gene_id": "EBG00000313325",
+            "gene_name": "rrs",
+            "feature_id": "EBG00000313325",
+            "type": "non_coding_transcript_exon_variant",
+            "change": "n.700A>T",
+            "nucleotide_change": "n.700A>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "n.700A>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "n.700A>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "n.700A>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "n.700A>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "EBG00000313325",
+                    "gene_name": "rrs",
+                    "feature_id": "EBG00000313325",
+                    "type": "non_coding_transcript_exon_variant",
+                    "nucleotide_change": "n.700A>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1472545A>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "n.700A>T",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
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+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "n.1507C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "n.1507C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "n.1507C>T",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
+                    "feature_id": "EBG00000313339",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "n.-306C>T",
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+                    "sequence_hgvs": "Chromosome:g.1473352C>T",
+                    "annotation": []
+                },
+                {
+                    "gene_id": "EBG00000313325",
+                    "gene_name": "rrs",
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+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1473352C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "n.1507C>T",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.1507C>T",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "n.1507C>T",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "n.1507C>T",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "EBG00000313325",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin",
+                "streptomycin"
+            ]
+        },
+        {
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+            "change": "n.1497C>A",
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+                    "type": "who_confidence",
+                    "drug": "capreomycin",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "linezolid",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
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+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1475154C>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.1497C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "linezolid",
+                            "original_mutation": "n.1497C>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "EBG00000313339",
+            "gene_associated_drugs": [
+                "capreomycin",
+                "linezolid"
+            ]
+        },
+        {
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+                    "type": "who_confidence",
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+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "linezolid",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
+                    "feature_id": "EBG00000313339",
+                    "type": "non_coding_transcript_exon_variant",
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+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1476481T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.2824T>C",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "linezolid",
+                            "original_mutation": "n.2824T>C",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "EBG00000313339",
+            "gene_associated_drugs": [
+                "capreomycin",
+                "linezolid"
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+            "feature_id": "Rv1484",
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+                {
+                    "type": "who_confidence",
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+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                {
+                    "gene_id": "Rv1484",
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+                    "feature_id": "Rv1484",
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+                    "sequence_hgvs": "Chromosome:g.1673349G>C",
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+                "ethionamide",
+                "isoniazid"
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+                    "type": "who_confidence",
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+                },
+                {
+                    "type": "who_confidence",
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+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                    "gene_id": "Rv1484",
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+                "ethionamide",
+                "isoniazid"
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+                    "confidence": "Not assoc w R - Interim",
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+            ],
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+                {
+                    "gene_id": "Rv1630",
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+                    "sequence_hgvs": "Chromosome:g.1834177A>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.636A>C",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+                    ]
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+                "pyrazinamide"
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+                    "sequence_hgvs": "Chromosome:g.1854300T>C",
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+                        {
+                            "type": "who_confidence",
+                            "drug": "linezolid",
+                            "original_mutation": "p.Leu232Pro",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+                "linezolid"
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+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "c.33A>G",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+                "capreomycin"
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+                        {
+                            "type": "who_confidence",
+                            "drug": "ethionamide",
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+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
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+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
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+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
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+                "delamanid",
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+            "protein_change": "p.Arg463Leu",
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+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "p.Arg463Leu",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
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+                    "type": "who_confidence",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
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+                    "gene_id": "Rv1908c",
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+                    "sequence_hgvs": "Chromosome:g.2156618G>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "isoniazid",
+                            "original_mutation": "c.-507C>G",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
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+                }
+            ],
+            "locus_tag": "Rv1908c",
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+                "isoniazid"
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+                    "type": "who_confidence",
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+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
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+                {
+                    "gene_id": "Rv1918c",
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+                    "feature_id": "Rv1918c",
+                    "type": "synonymous_variant",
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+                    "protein_change": "p.Leu916Leu",
+                    "sequence_hgvs": "Chromosome:g.2167865C>G",
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+                }
+            ],
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+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "change": "c.2745A>C",
+            "nucleotide_change": "c.2745A>C",
+            "protein_change": "p.Gly915Gly",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
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+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
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+                    "sequence_hgvs": "Chromosome:g.2167868T>G",
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+            ],
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+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "feature_id": "Rv1918c",
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+            "change": "p.Leu896Ser",
+            "nucleotide_change": "c.2687T>C",
+            "protein_change": "p.Leu896Ser",
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+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "p.Leu896Ser",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
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+                }
+            ],
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+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
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+                    "sequence_hgvs": "Chromosome:g.2167926A>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "p.Leu896Ser",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv1918c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "change": "p.Ala883Gly",
+            "nucleotide_change": "c.2648C>G",
+            "protein_change": "p.Ala883Gly",
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+                {
+                    "type": "who_confidence",
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+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.2648C>G",
+                    "protein_change": "p.Ala883Gly",
+                    "sequence_hgvs": "Chromosome:g.2167965G>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv1918c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
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+            "ref": "T",
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+            "type": "synonymous_variant",
+            "change": "c.2646A>C",
+            "nucleotide_change": "c.2646A>C",
+            "protein_change": "p.Pro882Pro",
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+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
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+                }
+            ],
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+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
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+                    "protein_change": "p.Pro882Pro",
+                    "sequence_hgvs": "Chromosome:g.2167967T>G",
+                    "annotation": []
+                }
+            ],
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+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
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+            "feature_id": "Rv1918c",
+            "type": "synonymous_variant",
+            "change": "c.1344A>G",
+            "nucleotide_change": "c.1344A>G",
+            "protein_change": "p.Gln448Gln",
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+                {
+                    "type": "who_confidence",
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+                {
+                    "gene_id": "Rv1918c",
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+                    "protein_change": "p.Gln448Gln",
+                    "sequence_hgvs": "Chromosome:g.2169269T>C",
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+                }
+            ],
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+                "pyrazinamide"
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+        {
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+            "type": "synonymous_variant",
+            "change": "c.1341C>G",
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+            "protein_change": "p.Gly447Gly",
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+                {
+                    "type": "who_confidence",
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+            ],
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+                    "sequence_hgvs": "Chromosome:g.2169272G>C",
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+                }
+            ],
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+                "pyrazinamide"
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+        },
+        {
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+            "type": "synonymous_variant",
+            "change": "c.1320T>C",
+            "nucleotide_change": "c.1320T>C",
+            "protein_change": "p.Gly440Gly",
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+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
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+            ],
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+                "pyrazinamide"
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+        },
+        {
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+            "type": "missense_variant",
+            "change": "p.Leu237Phe",
+            "nucleotide_change": "c.709_711delCTGinsTTC",
+            "protein_change": "p.Leu237Phe",
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+                {
+                    "type": "who_confidence",
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+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
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+                    "protein_change": "p.Leu237Phe",
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+            ],
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+                "pyrazinamide"
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+        {
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+            "type": "missense_variant",
+            "change": "p.Asn235Tyr",
+            "nucleotide_change": "c.703A>T",
+            "protein_change": "p.Asn235Tyr",
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+                {
+                    "type": "who_confidence",
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+                    "comment": "Not found in WHO catalogue",
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+                {
+                    "gene_id": "Rv1918c",
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+                    "protein_change": "p.Asn235Tyr",
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+                "pyrazinamide"
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+        {
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+            "type": "missense_variant",
+            "change": "p.Leu189Val",
+            "nucleotide_change": "c.565C>G",
+            "protein_change": "p.Leu189Val",
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+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
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+                {
+                    "gene_id": "Rv1918c",
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+            ],
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+                "pyrazinamide"
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+        {
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+            "type": "missense_variant",
+            "change": "p.Thr187Ser",
+            "nucleotide_change": "c.560C>G",
+            "protein_change": "p.Thr187Ser",
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+                {
+                    "type": "who_confidence",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
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+                    "nucleotide_change": "c.560C>G",
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+                    "sequence_hgvs": "Chromosome:g.2170053G>C",
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+            ],
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+                "pyrazinamide"
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+            "type": "missense_variant",
+            "change": "p.Ser156Ala",
+            "nucleotide_change": "c.466T>G",
+            "protein_change": "p.Ser156Ala",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.466T>G",
+                    "protein_change": "p.Ser156Ala",
+                    "sequence_hgvs": "Chromosome:g.2170147A>C",
+                    "annotation": []
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+            ],
+            "locus_tag": "Rv1918c",
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+                "pyrazinamide"
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+            "change": "c.-129A>G",
+            "nucleotide_change": "c.-129A>G",
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+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
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+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
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+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
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+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
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+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv1979c",
+                    "gene_name": "Rv1979c",
+                    "feature_id": "Rv1979c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-129A>G",
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+                    "sequence_hgvs": "Chromosome:g.2223293T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "c.-129A>G",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "c.-129A>G",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+                    ]
+                }
+            ],
+            "locus_tag": "Rv1979c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
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+            "gene_id": "Rv2245",
+            "gene_name": "kasA",
+            "feature_id": "Rv2245",
+            "type": "missense_variant",
+            "change": "p.Lys232Arg",
+            "nucleotide_change": "c.695A>G",
+            "protein_change": "p.Lys232Arg",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "isoniazid",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
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+                {
+                    "gene_id": "Rv2245",
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+                    "feature_id": "Rv2245",
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+                    "nucleotide_change": "c.695A>G",
+                    "protein_change": "p.Lys232Arg",
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+            ],
+            "locus_tag": "Rv2245",
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+                "isoniazid"
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+        {
+            "chrom": "Chromosome",
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+            "reverse_reads": 57,
+            "sv_len": null,
+            "gene_id": "Rv2780",
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+            "feature_id": "Rv2780",
+            "type": "upstream_gene_variant",
+            "change": "c.-32T>C",
+            "nucleotide_change": "c.-32T>C",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "cycloserine",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv2780",
+                    "gene_name": "ald",
+                    "feature_id": "Rv2780",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-32T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.3086788T>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv2780",
+            "gene_associated_drugs": [
+                "cycloserine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3087532,
+            "ref": "C",
+            "alt": "A",
+            "depth": 52,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 24,
+            "reverse_reads": 28,
+            "sv_len": null,
+            "gene_id": "Rv2780",
+            "gene_name": "ald",
+            "feature_id": "Rv2780",
+            "type": "missense_variant",
+            "change": "p.Ala238Asp",
+            "nucleotide_change": "c.713C>A",
+            "protein_change": "p.Ala238Asp",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "cycloserine",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv2780",
+                    "gene_name": "ald",
+                    "feature_id": "Rv2780",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.713C>A",
+                    "protein_change": "p.Ala238Asp",
+                    "sequence_hgvs": "Chromosome:g.3087532C>A",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv2780",
+            "gene_associated_drugs": [
+                "cycloserine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3612229,
+            "ref": "G",
+            "alt": "A",
+            "depth": 36,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 21,
+            "reverse_reads": 15,
+            "sv_len": null,
+            "gene_id": "Rv3236c",
+            "gene_name": "Rv3236c",
+            "feature_id": "Rv3236c",
+            "type": "synonymous_variant",
+            "change": "c.888C>T",
+            "nucleotide_change": "c.888C>T",
+            "protein_change": "p.Ala296Ala",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "c.888C>T",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3236c",
+                    "gene_name": "Rv3236c",
+                    "feature_id": "Rv3236c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.888C>T",
+                    "protein_change": "p.Ala296Ala",
+                    "sequence_hgvs": "Chromosome:g.3612229G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.888C>T",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3236c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3612813,
+            "ref": "T",
+            "alt": "C",
+            "depth": 19,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 9,
+            "reverse_reads": 10,
+            "sv_len": null,
+            "gene_id": "Rv3236c",
+            "gene_name": "Rv3236c",
+            "feature_id": "Rv3236c",
+            "type": "missense_variant",
+            "change": "p.Thr102Ala",
+            "nucleotide_change": "c.304A>G",
+            "protein_change": "p.Thr102Ala",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "original_mutation": "p.Thr102Ala",
+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3236c",
+                    "gene_name": "Rv3236c",
+                    "feature_id": "Rv3236c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.304A>G",
+                    "protein_change": "p.Thr102Ala",
+                    "sequence_hgvs": "Chromosome:g.3612813T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "p.Thr102Ala",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3236c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3625065,
+            "ref": "T",
+            "alt": "G",
+            "depth": 17,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 10,
+            "reverse_reads": 7,
+            "sv_len": null,
+            "gene_id": "Rv3245c",
+            "gene_name": "mtrB",
+            "feature_id": "Rv3245c",
+            "type": "missense_variant",
+            "change": "p.Met517Leu",
+            "nucleotide_change": "c.1549A>C",
+            "protein_change": "p.Met517Leu",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.Met517Leu",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Met517Leu",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3245c",
+                    "gene_name": "mtrB",
+                    "feature_id": "Rv3245c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1549A>C",
+                    "protein_change": "p.Met517Leu",
+                    "sequence_hgvs": "Chromosome:g.3625065T>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.Met517Leu",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "p.Met517Leu",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                },
+                {
+                    "gene_id": "Rv3244c",
+                    "gene_name": "lpqB",
+                    "feature_id": "Rv3244c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-155A>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.3625065T>G",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3245c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3626562,
+            "ref": "G",
+            "alt": "A",
+            "depth": 21,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 12,
+            "reverse_reads": 9,
+            "sv_len": null,
+            "gene_id": "Rv3245c",
+            "gene_name": "mtrB",
+            "feature_id": "Rv3245c",
+            "type": "missense_variant",
+            "change": "p.Pro18Ser",
+            "nucleotide_change": "c.52C>T",
+            "protein_change": "p.Pro18Ser",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.Pro18Ser",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "rifampicin",
+                    "original_mutation": "p.Pro18Ser",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3245c",
+                    "gene_name": "mtrB",
+                    "feature_id": "Rv3245c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.52C>T",
+                    "protein_change": "p.Pro18Ser",
+                    "sequence_hgvs": "Chromosome:g.3626562G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.Pro18Ser",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "rifampicin",
+                            "original_mutation": "p.Pro18Ser",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3245c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "rifampicin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 3841546,
+            "ref": "G",
+            "alt": "T",
+            "depth": 68,
+            "freq": 0.19117647058823528,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 8,
+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "Rv3423c",
+            "gene_name": "alr",
+            "feature_id": "Rv3423c",
+            "type": "upstream_gene_variant",
+            "change": "c.-198C>A",
+            "nucleotide_change": "c.-198C>A",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "cycloserine",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3423c",
+                    "gene_name": "alr",
+                    "feature_id": "Rv3423c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-198C>A",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.3841546G>T",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3423c",
+            "gene_associated_drugs": [
+                "cycloserine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4038776,
+            "ref": "C",
+            "alt": "G",
+            "depth": 81,
+            "freq": 0.1111111111111111,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 5,
+            "reverse_reads": 4,
+            "sv_len": null,
+            "gene_id": "Rv3596c",
+            "gene_name": "clpC1",
+            "feature_id": "Rv3596c",
+            "type": "missense_variant",
+            "change": "p.Glu643Asp",
+            "nucleotide_change": "c.1929G>C",
+            "protein_change": "p.Glu643Asp",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3596c",
+                    "gene_name": "clpC1",
+                    "feature_id": "Rv3596c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1929G>C",
+                    "protein_change": "p.Glu643Asp",
+                    "sequence_hgvs": "Chromosome:g.4038776C>G",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3596c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4039714,
+            "ref": "A",
+            "alt": "G",
+            "depth": 58,
+            "freq": 0.15517241379310345,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 4,
+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "Rv3596c",
+            "gene_name": "clpC1",
+            "feature_id": "Rv3596c",
+            "type": "missense_variant",
+            "change": "p.Tyr331His",
+            "nucleotide_change": "c.991T>C",
+            "protein_change": "p.Tyr331His",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3596c",
+                    "gene_name": "clpC1",
+                    "feature_id": "Rv3596c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.991T>C",
+                    "protein_change": "p.Tyr331His",
+                    "sequence_hgvs": "Chromosome:g.4039714A>G",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3596c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4039730,
+            "ref": "G",
+            "alt": "C",
+            "depth": 54,
+            "freq": 0.18518518518518517,
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+            "filter": "pass",
+            "forward_reads": 4,
+            "reverse_reads": 6,
+            "sv_len": null,
+            "gene_id": "Rv3596c",
+            "gene_name": "clpC1",
+            "feature_id": "Rv3596c",
+            "type": "synonymous_variant",
+            "change": "c.975C>G",
+            "nucleotide_change": "c.975C>G",
+            "protein_change": "p.Leu325Leu",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3596c",
+                    "gene_name": "clpC1",
+                    "feature_id": "Rv3596c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.975C>G",
+                    "protein_change": "p.Leu325Leu",
+                    "sequence_hgvs": "Chromosome:g.4039730G>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3596c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4040057,
+            "ref": "G",
+            "alt": "A",
+            "depth": 38,
+            "freq": 0.23684210526315788,
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+            "filter": "pass",
+            "forward_reads": 4,
+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "Rv3596c",
+            "gene_name": "clpC1",
+            "feature_id": "Rv3596c",
+            "type": "synonymous_variant",
+            "change": "c.648C>T",
+            "nucleotide_change": "c.648C>T",
+            "protein_change": "p.Gly216Gly",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "pyrazinamide",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3596c",
+                    "gene_name": "clpC1",
+                    "feature_id": "Rv3596c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.648C>T",
+                    "protein_change": "p.Gly216Gly",
+                    "sequence_hgvs": "Chromosome:g.4040057G>A",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3596c",
+            "gene_associated_drugs": [
+                "pyrazinamide"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4242643,
+            "ref": "C",
+            "alt": "T",
+            "depth": 15,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 7,
+            "reverse_reads": 8,
+            "sv_len": null,
+            "gene_id": "Rv3793",
+            "gene_name": "embC",
+            "feature_id": "Rv3793",
+            "type": "synonymous_variant",
+            "change": "c.2781C>T",
+            "nucleotide_change": "c.2781C>T",
+            "protein_change": "p.Arg927Arg",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethambutol",
+                    "original_mutation": "c.2781C>T",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3793",
+                    "gene_name": "embC",
+                    "feature_id": "Rv3793",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.2781C>T",
+                    "protein_change": "p.Arg927Arg",
+                    "sequence_hgvs": "Chromosome:g.4242643C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethambutol",
+                            "original_mutation": "c.2781C>T",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                },
+                {
+                    "gene_id": "Rv3794",
+                    "gene_name": "embA",
+                    "feature_id": "Rv3794",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-590C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.4242643C>T",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3793",
+            "gene_associated_drugs": [
+                "ethambutol"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4243460,
+            "ref": "C",
+            "alt": "T",
+            "depth": 28,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 15,
+            "reverse_reads": 13,
+            "sv_len": null,
+            "gene_id": "Rv3794",
+            "gene_name": "embA",
+            "feature_id": "Rv3794",
+            "type": "synonymous_variant",
+            "change": "c.228C>T",
+            "nucleotide_change": "c.228C>T",
+            "protein_change": "p.Cys76Cys",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethambutol",
+                    "original_mutation": "c.228C>T",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3794",
+                    "gene_name": "embA",
+                    "feature_id": "Rv3794",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.228C>T",
+                    "protein_change": "p.Cys76Cys",
+                    "sequence_hgvs": "Chromosome:g.4243460C>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethambutol",
+                            "original_mutation": "c.228C>T",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3794",
+            "gene_associated_drugs": [
+                "ethambutol"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4267647,
+            "ref": "T",
+            "alt": "C",
+            "depth": 15,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 8,
+            "reverse_reads": 7,
+            "sv_len": null,
+            "gene_id": "Rv3805c",
+            "gene_name": "aftB",
+            "feature_id": "Rv3805c",
+            "type": "missense_variant",
+            "change": "p.Asp397Gly",
+            "nucleotide_change": "c.1190A>G",
+            "protein_change": "p.Asp397Gly",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "ethambutol",
+                    "original_mutation": "p.Asp397Gly",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3805c",
+                    "gene_name": "aftB",
+                    "feature_id": "Rv3805c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1190A>G",
+                    "protein_change": "p.Asp397Gly",
+                    "sequence_hgvs": "Chromosome:g.4267647T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "ethambutol",
+                            "original_mutation": "p.Asp397Gly",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3805c",
+            "gene_associated_drugs": [
+                "ethambutol"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4338595,
+            "ref": "GC",
+            "alt": "G",
+            "depth": 62,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 34,
+            "reverse_reads": 28,
+            "sv_len": null,
+            "gene_id": "Rv3862c",
+            "gene_name": "whiB6",
+            "feature_id": "Rv3862c",
+            "type": "upstream_gene_variant",
+            "change": "c.-75delG",
+            "nucleotide_change": "c.-75delG",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "c.-75delG",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "c.-75delG",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "c.-75delG",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3862c",
+                    "gene_name": "whiB6",
+                    "feature_id": "Rv3862c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-75delG",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.4338595GC>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "c.-75delG",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "c.-75delG",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "c.-75delG",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3862c",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4338732,
+            "ref": "G",
+            "alt": "A",
+            "depth": 89,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 49,
+            "reverse_reads": 40,
+            "sv_len": null,
+            "gene_id": "Rv3862c",
+            "gene_name": "whiB6",
+            "feature_id": "Rv3862c",
+            "type": "upstream_gene_variant",
+            "change": "c.-211C>T",
+            "nucleotide_change": "c.-211C>T",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "confidence": "Uncertain significance",
+                    "comment": "Not found in WHO catalogue",
+                    "source": "",
+                    "original_mutation": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3862c",
+                    "gene_name": "whiB6",
+                    "feature_id": "Rv3862c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-211C>T",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.4338732G>A",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv3862c",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4407588,
+            "ref": "T",
+            "alt": "C",
+            "depth": 21,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 11,
+            "reverse_reads": 10,
+            "sv_len": null,
+            "gene_id": "Rv3919c",
+            "gene_name": "gid",
+            "feature_id": "Rv3919c",
+            "type": "synonymous_variant",
+            "change": "c.615A>G",
+            "nucleotide_change": "c.615A>G",
+            "protein_change": "p.Ala205Ala",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "c.615A>G",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3919c",
+                    "gene_name": "gid",
+                    "feature_id": "Rv3919c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.615A>G",
+                    "protein_change": "p.Ala205Ala",
+                    "sequence_hgvs": "Chromosome:g.4407588T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "c.615A>G",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3919c",
+            "gene_associated_drugs": [
+                "streptomycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 4407927,
+            "ref": "T",
+            "alt": "G",
+            "depth": 34,
+            "freq": 1.0,
+            "sv": false,
+            "filter": "pass",
+            "forward_reads": 18,
+            "reverse_reads": 16,
+            "sv_len": null,
+            "gene_id": "Rv3919c",
+            "gene_name": "gid",
+            "feature_id": "Rv3919c",
+            "type": "missense_variant",
+            "change": "p.Glu92Asp",
+            "nucleotide_change": "c.276A>C",
+            "protein_change": "p.Glu92Asp",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "p.Glu92Asp",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv3919c",
+                    "gene_name": "gid",
+                    "feature_id": "Rv3919c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.276A>C",
+                    "protein_change": "p.Glu92Asp",
+                    "sequence_hgvs": "Chromosome:g.4407927T>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "p.Glu92Asp",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv3919c",
+            "gene_associated_drugs": [
+                "streptomycin"
+            ]
+        }
+    ],
+    "qc_fail_variants": [
+        {
+            "chrom": "Chromosome",
+            "pos": 619784,
+            "ref": "G",
+            "alt": "A",
+            "depth": 16,
+            "freq": 0.125,
+            "sv": false,
+            "filter": "soft_fail",
+            "forward_reads": 1,
+            "reverse_reads": 1,
+            "sv_len": null,
+            "gene_id": "Rv0529",
+            "gene_name": "ccsA",
+            "feature_id": "Rv0529",
+            "type": "upstream_gene_variant",
+            "change": "c.-107G>A",
+            "nucleotide_change": "c.-107G>A",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "c.-107G>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
+                    "original_mutation": "c.-107G>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "c.-107G>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0529",
+                    "gene_name": "ccsA",
+                    "feature_id": "Rv0529",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-107G>A",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.619784G>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "c.-107G>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "c.-107G>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "c.-107G>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0529",
+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 737427,
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+            "alt": "G",
+            "depth": 113,
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+            "forward_reads": 6,
+            "reverse_reads": 5,
+            "sv_len": null,
+            "gene_id": "Rv0643c",
+            "gene_name": "mmaA3",
+            "feature_id": "Rv0643c",
+            "type": "synonymous_variant",
+            "change": "c.723T>C",
+            "nucleotide_change": "c.723T>C",
+            "protein_change": "p.Thr241Thr",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv0643c",
+                    "gene_name": "mmaA3",
+                    "feature_id": "Rv0643c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.723T>C",
+                    "protein_change": "p.Thr241Thr",
+                    "sequence_hgvs": "Chromosome:g.737427A>G",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0643c",
+            "gene_associated_drugs": [
+                "isoniazid"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 777119,
+            "ref": "G",
+            "alt": "T",
+            "depth": 68,
+            "freq": 0.10294117647058823,
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+            "filter": "soft_fail",
+            "forward_reads": 5,
+            "reverse_reads": 2,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "missense_variant",
+            "change": "p.His454Gln",
+            "nucleotide_change": "c.1362C>A",
+            "protein_change": "p.His454Gln",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "bedaquiline",
+                    "original_mutation": "p.His454Gln",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "clofazimine",
+                    "original_mutation": "p.His454Gln",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1362C>A",
+                    "protein_change": "p.His454Gln",
+                    "sequence_hgvs": "Chromosome:g.777119G>T",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "bedaquiline",
+                            "original_mutation": "p.His454Gln",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "clofazimine",
+                            "original_mutation": "p.His454Gln",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 777122,
+            "ref": "G",
+            "alt": "A",
+            "depth": 66,
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+            "filter": "soft_fail",
+            "forward_reads": 5,
+            "reverse_reads": 2,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "synonymous_variant",
+            "change": "c.1359C>T",
+            "nucleotide_change": "c.1359C>T",
+            "protein_change": "p.Asp453Asp",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.1359C>T",
+                    "protein_change": "p.Asp453Asp",
+                    "sequence_hgvs": "Chromosome:g.777122G>A",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 777262,
+            "ref": "T",
+            "alt": "C",
+            "depth": 16,
+            "freq": 0.125,
+            "sv": false,
+            "filter": "soft_fail",
+            "forward_reads": 1,
+            "reverse_reads": 1,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "missense_variant",
+            "change": "p.Thr407Ala",
+            "nucleotide_change": "c.1219A>G",
+            "protein_change": "p.Thr407Ala",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "missense_variant",
+                    "nucleotide_change": "c.1219A>G",
+                    "protein_change": "p.Thr407Ala",
+                    "sequence_hgvs": "Chromosome:g.777262T>C",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
+            ]
+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 777263,
+            "ref": "C",
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+            "sv": false,
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+            "reverse_reads": 1,
+            "sv_len": null,
+            "gene_id": "Rv0676c",
+            "gene_name": "mmpL5",
+            "feature_id": "Rv0676c",
+            "type": "synonymous_variant",
+            "change": "c.1218G>C",
+            "nucleotide_change": "c.1218G>C",
+            "protein_change": "p.Leu406Leu",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv0676c",
+                    "gene_name": "mmpL5",
+                    "feature_id": "Rv0676c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.1218G>C",
+                    "protein_change": "p.Leu406Leu",
+                    "sequence_hgvs": "Chromosome:g.777263C>G",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv0676c",
+            "gene_associated_drugs": [
+                "bedaquiline",
+                "clofazimine"
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+        {
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+            "gene_id": "Rv1173",
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+            "change": "c.1035G>A",
+            "nucleotide_change": "c.1035G>A",
+            "protein_change": "p.Ala345Ala",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv1173",
+                    "gene_name": "fbiC",
+                    "feature_id": "Rv1173",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.1035G>A",
+                    "protein_change": "p.Ala345Ala",
+                    "sequence_hgvs": "Chromosome:g.1303965G>A",
+                    "annotation": []
+                }
+            ],
+            "locus_tag": "Rv1173",
+            "gene_associated_drugs": [
+                "clofazimine",
+                "delamanid",
+                "pretomanid"
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+        },
+        {
+            "chrom": "Chromosome",
+            "pos": 1407545,
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+            "depth": 8,
+            "freq": 0.25,
+            "sv": false,
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+            "reverse_reads": 1,
+            "sv_len": null,
+            "gene_id": "Rv1258c",
+            "gene_name": "Rv1258c",
+            "feature_id": "Rv1258c",
+            "type": "upstream_gene_variant",
+            "change": "c.-205T>C",
+            "nucleotide_change": "c.-205T>C",
+            "protein_change": "",
+            "annotation": [],
+            "consequences": [
+                {
+                    "gene_id": "Rv1258c",
+                    "gene_name": "Rv1258c",
+                    "feature_id": "Rv1258c",
+                    "type": "upstream_gene_variant",
+                    "nucleotide_change": "c.-205T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1407545A>G",
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+            "locus_tag": "Rv1258c",
+            "gene_associated_drugs": [
+                "isoniazid",
+                "pyrazinamide",
+                "streptomycin"
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+        {
+            "chrom": "Chromosome",
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+            "depth": 29,
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+            "filter": "soft_fail",
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+            "sv_len": null,
+            "gene_id": "EBG00000313325",
+            "gene_name": "rrs",
+            "feature_id": "EBG00000313325",
+            "type": "non_coding_transcript_exon_variant",
+            "change": "n.292G>A",
+            "nucleotide_change": "n.292G>A",
+            "protein_change": "",
+            "annotation": [
+                {
+                    "type": "who_confidence",
+                    "drug": "amikacin",
+                    "original_mutation": "n.292G>A",
+                    "confidence": "Not assoc w R",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
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+                    "original_mutation": "n.1217T>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
+                    "original_mutation": "n.1217T>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "streptomycin",
+                    "original_mutation": "n.1217T>A",
+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                }
+            ],
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
+                    "feature_id": "EBG00000313339",
+                    "type": "upstream_gene_variant",
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+                    "sequence_hgvs": "Chromosome:g.1473062T>A",
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+                {
+                    "gene_id": "EBG00000313325",
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+                    "sequence_hgvs": "Chromosome:g.1473062T>A",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "n.1217T>A",
+                            "confidence": "Not assoc w R",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.1217T>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "n.1217T>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "n.1217T>A",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
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+                "amikacin",
+                "capreomycin",
+                "kanamycin",
+                "streptomycin"
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+        {
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+            "change": "n.1360T>C",
+            "nucleotide_change": "n.1360T>C",
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+            "annotation": [
+                {
+                    "type": "who_confidence",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
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+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "capreomycin",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
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+                },
+                {
+                    "type": "who_confidence",
+                    "drug": "kanamycin",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
+                    "comment": ""
+                },
+                {
+                    "type": "who_confidence",
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+                    "confidence": "Uncertain significance",
+                    "source": "WHO catalogue v2",
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+                }
+            ],
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
+                    "feature_id": "EBG00000313339",
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+                    "sequence_hgvs": "Chromosome:g.1473205T>C",
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+                },
+                {
+                    "gene_id": "EBG00000313325",
+                    "gene_name": "rrs",
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+                    "nucleotide_change": "n.1360T>C",
+                    "protein_change": "",
+                    "sequence_hgvs": "Chromosome:g.1473205T>C",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "amikacin",
+                            "original_mutation": "n.1360T>C",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "capreomycin",
+                            "original_mutation": "n.1360T>C",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "kanamycin",
+                            "original_mutation": "n.1360T>C",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        },
+                        {
+                            "type": "who_confidence",
+                            "drug": "streptomycin",
+                            "original_mutation": "n.1360T>C",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
+                        }
+                    ]
+                }
+            ],
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+            "gene_associated_drugs": [
+                "amikacin",
+                "capreomycin",
+                "kanamycin",
+                "streptomycin"
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+        {
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
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+                    "sequence_hgvs": "Chromosome:g.1474267G>A",
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+                "capreomycin",
+                "linezolid"
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+        {
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
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+                    "sequence_hgvs": "Chromosome:g.1474774A>G",
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+                "capreomycin",
+                "linezolid"
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+        {
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+            "change": "n.1172delC",
+            "nucleotide_change": "n.1172delC",
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+                {
+                    "gene_id": "EBG00000313339",
+                    "gene_name": "rrl",
+                    "feature_id": "EBG00000313339",
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+                    "sequence_hgvs": "Chromosome:g.1474828GC>G",
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+                "capreomycin",
+                "linezolid"
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+            "change": "n.1518G>T",
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+                {
+                    "gene_id": "EBG00000313339",
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+                    "sequence_hgvs": "Chromosome:g.1475175G>T",
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+                "capreomycin",
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+            "protein_change": "p.Leu11Met",
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+                {
+                    "gene_id": "Rv1694",
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+            "change": "p.Asp714Glu",
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+            "protein_change": "p.Asp714Glu",
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+                {
+                    "gene_id": "Rv1908c",
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+            "change": "p.Asp74Tyr",
+            "nucleotide_change": "c.220G>T",
+            "protein_change": "p.Asp74Tyr",
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+                {
+                    "gene_id": "Rv1908c",
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+                    "protein_change": "p.Asp74Tyr",
+                    "sequence_hgvs": "Chromosome:g.2155892C>A",
+                    "annotation": [
+                        {
+                            "type": "drug_resistance",
+                            "drug": "isoniazid",
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+                            "source": "tbdb",
+                            "comment": "Mutation from literature"
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+                "isoniazid"
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+                    "type": "who_confidence",
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+                    "confidence": "Not assoc w R - Interim",
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+                    "sequence_hgvs": "Chromosome:g.2169170G>C",
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+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.1443C>G",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+            "locus_tag": "Rv1918c",
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+                "pyrazinamide"
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+            "change": "p.Ala152Ser",
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+            "protein_change": "p.Ala152Ser",
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+                {
+                    "gene_id": "Rv1918c",
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+                    "protein_change": "p.Ala152Ser",
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+                "pyrazinamide"
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+            "gene_id": "Rv1918c",
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+            "type": "missense_variant",
+            "change": "p.Leu102Ala",
+            "nucleotide_change": "c.304_305delCTinsGC",
+            "protein_change": "p.Leu102Ala",
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+                {
+                    "type": "who_confidence",
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+                    "confidence": "Uncertain significance",
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+                {
+                    "gene_id": "Rv1918c",
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+                    "protein_change": "p.Leu102Ala",
+                    "sequence_hgvs": "Chromosome:g.2170308AG>GC",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "p.Leu102Ala",
+                            "confidence": "Uncertain significance",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+            "locus_tag": "Rv1918c",
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+                "pyrazinamide"
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+        {
+            "chrom": "Chromosome",
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+            "type": "synonymous_variant",
+            "change": "c.300G>C",
+            "nucleotide_change": "c.300G>C",
+            "protein_change": "p.Val100Val",
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+                {
+                    "type": "who_confidence",
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+                    "confidence": "Not assoc w R - Interim",
+                    "source": "WHO catalogue v2",
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+            ],
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+                {
+                    "gene_id": "Rv1918c",
+                    "gene_name": "PPE35",
+                    "feature_id": "Rv1918c",
+                    "type": "synonymous_variant",
+                    "nucleotide_change": "c.300G>C",
+                    "protein_change": "p.Val100Val",
+                    "sequence_hgvs": "Chromosome:g.2170313C>G",
+                    "annotation": [
+                        {
+                            "type": "who_confidence",
+                            "drug": "pyrazinamide",
+                            "original_mutation": "c.300G>C",
+                            "confidence": "Not assoc w R - Interim",
+                            "source": "WHO catalogue v2",
+                            "comment": ""
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+            ],
+            "locus_tag": "Rv1918c",
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+                "pyrazinamide"
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+                "median_depth": 43.0
+            },
+            {
+                "target": "Rv3236c",
+                "percent_depth_pass": 99.15,
+                "median_depth": 30.0
+            },
+            {
+                "target": "lpqB",
+                "percent_depth_pass": 98.41,
+                "median_depth": 28.0
+            },
+            {
+                "target": "mtrB",
+                "percent_depth_pass": 100.0,
+                "median_depth": 32.0
+            },
+            {
+                "target": "mtrA",
+                "percent_depth_pass": 100.0,
+                "median_depth": 39.0
+            },
+            {
+                "target": "fbiA",
+                "percent_depth_pass": 100.0,
+                "median_depth": 38.0
+            },
+            {
+                "target": "fbiB",
+                "percent_depth_pass": 100.0,
+                "median_depth": 29.0
+            },
+            {
+                "target": "alr",
+                "percent_depth_pass": 100.0,
+                "median_depth": 43.0
+            },
+            {
+                "target": "rpoA",
+                "percent_depth_pass": 95.95,
+                "median_depth": 46.0
+            },
+            {
+                "target": "ddn",
+                "percent_depth_pass": 100.0,
+                "median_depth": 46.0
+            },
+            {
+                "target": "clpC1",
+                "percent_depth_pass": 100.0,
+                "median_depth": 51.0
+            },
+            {
+                "target": "panD",
+                "percent_depth_pass": 99.49,
+                "median_depth": 30.0
+            },
+            {
+                "target": "glpK",
+                "percent_depth_pass": 100.0,
+                "median_depth": 42.0
+            },
+            {
+                "target": "embC",
+                "percent_depth_pass": 97.88,
+                "median_depth": 30.0
+            },
+            {
+                "target": "embA",
+                "percent_depth_pass": 97.54,
+                "median_depth": 28.0
+            },
+            {
+                "target": "embB",
+                "percent_depth_pass": 100.0,
+                "median_depth": 31.0
+            },
+            {
+                "target": "aftB",
+                "percent_depth_pass": 99.77,
+                "median_depth": 32.0
+            },
+            {
+                "target": "ubiA",
+                "percent_depth_pass": 100.0,
+                "median_depth": 34.0
+            },
+            {
+                "target": "ethA",
+                "percent_depth_pass": 100.0,
+                "median_depth": 45.0
+            },
+            {
+                "target": "ethR",
+                "percent_depth_pass": 100.0,
+                "median_depth": 45.0
+            },
+            {
+                "target": "whiB6",
+                "percent_depth_pass": 99.87,
+                "median_depth": 71.0
+            },
+            {
+                "target": "gid",
+                "percent_depth_pass": 100.0,
+                "median_depth": 39.0
+            }
+        ],
+        "missing_positions": [
+            {
+                "chrom": "Chromosome",
+                "pos": 1304845,
+                "depth": 3,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "delamanid",
+                        "original_mutation": "p.Ala639fs",
+                        "confidence": "Assoc w R - Interim",
+                        "source": "WHO catalogue v2",
+                        "comment": "",
+                        "gene": "Rv1173",
+                        "variant": "p.Ala639fs"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 1304846,
+                "depth": 3,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "delamanid",
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+                        "confidence": "Assoc w R - Interim",
+                        "source": "WHO catalogue v2",
+                        "comment": "",
+                        "gene": "Rv1173",
+                        "variant": "p.Ala639fs"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 1304847,
+                "depth": 3,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "delamanid",
+                        "original_mutation": "p.Ala639fs",
+                        "confidence": "Assoc w R - Interim",
+                        "source": "WHO catalogue v2",
+                        "comment": "",
+                        "gene": "Rv1173",
+                        "variant": "p.Ala639fs"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 1917979,
+                "depth": 9,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "capreomycin",
+                        "original_mutation": "p.Arg14Trp",
+                        "confidence": "Uncertain significance",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv1694",
+                        "variant": "p.Arg14Trp"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 1917980,
+                "depth": 9,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "capreomycin",
+                        "original_mutation": "p.Arg14Trp",
+                        "confidence": "Uncertain significance",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv1694",
+                        "variant": "p.Arg14Trp"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4240622,
+                "depth": 8,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala254Gly",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3793",
+                        "variant": "p.Ala254Gly"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4240623,
+                "depth": 8,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala254Gly",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3793",
+                        "variant": "p.Ala254Gly"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4240624,
+                "depth": 8,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala254Gly",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3793",
+                        "variant": "p.Ala254Gly"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4244616,
+                "depth": 9,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala462Val",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3794",
+                        "variant": "p.Ala462Val"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4244617,
+                "depth": 9,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala462Val",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3794",
+                        "variant": "p.Ala462Val"
+                    }
+                ]
+            },
+            {
+                "chrom": "Chromosome",
+                "pos": 4244618,
+                "depth": 9,
+                "annotation": [
+                    {
+                        "type": "drug_resistance",
+                        "drug": "ethambutol",
+                        "original_mutation": "p.Ala462Val",
+                        "confidence": "",
+                        "source": "tbdb",
+                        "comment": "Mutation from literature",
+                        "gene": "Rv3794",
+                        "variant": "p.Ala462Val"
+                    }
+                ]
+            }
+        ]
+    },
+    "linked_samples": []
+}
\ No newline at end of file