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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 19-6744816-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=6744816&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 6744816,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001288962.2",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "NM_001288962.2",
"protein_id": "NP_001275891.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 601,
"cds_start": 806,
"cds_end": null,
"cds_length": 1806,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000313244.14",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001288962.2"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "ENST00000313244.14",
"protein_id": "ENSP00000320117.7",
"transcript_support_level": 1,
"aa_start": 269,
"aa_end": null,
"aa_length": 601,
"cds_start": 806,
"cds_end": null,
"cds_length": 1806,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001288962.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000313244.14"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "ENST00000596758.5",
"protein_id": "ENSP00000469360.1",
"transcript_support_level": 1,
"aa_start": 269,
"aa_end": null,
"aa_length": 593,
"cds_start": 806,
"cds_end": null,
"cds_length": 1782,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000596758.5"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "ENST00000313285.12",
"protein_id": "ENSP00000320493.6",
"transcript_support_level": 1,
"aa_start": 269,
"aa_end": null,
"aa_length": 545,
"cds_start": 806,
"cds_end": null,
"cds_length": 1638,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000313285.12"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.803T>C",
"hgvs_p": "p.Ile268Thr",
"transcript": "ENST00000943820.1",
"protein_id": "ENSP00000613879.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 600,
"cds_start": 803,
"cds_end": null,
"cds_length": 1803,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943820.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "NM_001288963.3",
"protein_id": "NP_001275892.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 593,
"cds_start": 806,
"cds_end": null,
"cds_length": 1782,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001288963.3"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.776T>C",
"hgvs_p": "p.Ile259Thr",
"transcript": "ENST00000894345.1",
"protein_id": "ENSP00000564404.1",
"transcript_support_level": null,
"aa_start": 259,
"aa_end": null,
"aa_length": 591,
"cds_start": 776,
"cds_end": null,
"cds_length": 1776,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894345.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.749T>C",
"hgvs_p": "p.Ile250Thr",
"transcript": "ENST00000894347.1",
"protein_id": "ENSP00000564406.1",
"transcript_support_level": null,
"aa_start": 250,
"aa_end": null,
"aa_length": 582,
"cds_start": 749,
"cds_end": null,
"cds_length": 1749,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894347.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.743T>C",
"hgvs_p": "p.Ile248Thr",
"transcript": "ENST00000943818.1",
"protein_id": "ENSP00000613877.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 580,
"cds_start": 743,
"cds_end": null,
"cds_length": 1743,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943818.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "ENST00000921001.1",
"protein_id": "ENSP00000591060.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 557,
"cds_start": 806,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921001.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.842T>C",
"hgvs_p": "p.Ile281Thr",
"transcript": "ENST00000943819.1",
"protein_id": "ENSP00000613878.1",
"transcript_support_level": null,
"aa_start": 281,
"aa_end": null,
"aa_length": 557,
"cds_start": 842,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943819.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "ENST00000943817.1",
"protein_id": "ENSP00000613876.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 550,
"cds_start": 806,
"cds_end": null,
"cds_length": 1653,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943817.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "NM_004240.4",
"protein_id": "NP_004231.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 545,
"cds_start": 806,
"cds_end": null,
"cds_length": 1638,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004240.4"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.803T>C",
"hgvs_p": "p.Ile268Thr",
"transcript": "ENST00000921000.1",
"protein_id": "ENSP00000591059.1",
"transcript_support_level": null,
"aa_start": 268,
"aa_end": null,
"aa_length": 544,
"cds_start": 803,
"cds_end": null,
"cds_length": 1635,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921000.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.776T>C",
"hgvs_p": "p.Ile259Thr",
"transcript": "ENST00000894346.1",
"protein_id": "ENSP00000564405.1",
"transcript_support_level": null,
"aa_start": 259,
"aa_end": null,
"aa_length": 535,
"cds_start": 776,
"cds_end": null,
"cds_length": 1608,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894346.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.746T>C",
"hgvs_p": "p.Ile249Thr",
"transcript": "ENST00000943821.1",
"protein_id": "ENSP00000613880.1",
"transcript_support_level": null,
"aa_start": 249,
"aa_end": null,
"aa_length": 525,
"cds_start": 746,
"cds_end": null,
"cds_length": 1578,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943821.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.743T>C",
"hgvs_p": "p.Ile248Thr",
"transcript": "ENST00000943816.1",
"protein_id": "ENSP00000613875.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 524,
"cds_start": 743,
"cds_end": null,
"cds_length": 1575,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943816.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.482T>C",
"hgvs_p": "p.Ile161Thr",
"transcript": "ENST00000600428.5",
"protein_id": "ENSP00000471203.1",
"transcript_support_level": 5,
"aa_start": 161,
"aa_end": null,
"aa_length": 437,
"cds_start": 482,
"cds_end": null,
"cds_length": 1314,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000600428.5"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "XM_006722940.2",
"protein_id": "XP_006723003.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 649,
"cds_start": 806,
"cds_end": null,
"cds_length": 1950,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006722940.2"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr",
"transcript": "XM_005259683.3",
"protein_id": "XP_005259740.1",
"transcript_support_level": null,
"aa_start": 269,
"aa_end": null,
"aa_length": 334,
"cds_start": 806,
"cds_end": null,
"cds_length": 1005,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005259683.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "n.841T>C",
"hgvs_p": null,
"transcript": "ENST00000595305.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000595305.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "n.1109T>C",
"hgvs_p": null,
"transcript": "ENST00000600491.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000600491.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "n.806T>C",
"hgvs_p": null,
"transcript": "ENST00000600677.5",
"protein_id": "ENSP00000472580.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000600677.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"hgvs_c": "n.888T>C",
"hgvs_p": null,
"transcript": "NR_110231.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_110231.2"
}
],
"gene_symbol": "TRIP10",
"gene_hgnc_id": 12304,
"dbsnp": "rs775226645",
"frequency_reference_population": 0.0000030982926,
"hom_count_reference_population": 0,
"allele_count_reference_population": 5,
"gnomad_exomes_af": 0.00000273677,
"gnomad_genomes_af": 0.0000065697,
"gnomad_exomes_ac": 4,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8334184885025024,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.1599999964237213,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.406,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.2826,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.09,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 7.572,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.16,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 3,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3",
"acmg_by_gene": [
{
"score": 3,
"benign_score": 0,
"pathogenic_score": 3,
"criteria": [
"PM2",
"PP3"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001288962.2",
"gene_symbol": "TRIP10",
"hgnc_id": 12304,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.806T>C",
"hgvs_p": "p.Ile269Thr"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}