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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: 15-74182370-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=74182370&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 74182370,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000395105.9",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "NM_022369.4",
"protein_id": "NP_071764.3",
"transcript_support_level": null,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1481,
"cdna_end": null,
"cdna_length": 2708,
"mane_select": "ENST00000395105.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "ENST00000395105.9",
"protein_id": "ENSP00000378537.4",
"transcript_support_level": 1,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1481,
"cdna_end": null,
"cdna_length": 2708,
"mane_select": "NM_022369.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1508T>G",
"hgvs_p": "p.Leu503Arg",
"transcript": "ENST00000563965.5",
"protein_id": "ENSP00000456609.1",
"transcript_support_level": 1,
"aa_start": 503,
"aa_end": null,
"aa_length": 706,
"cds_start": 1508,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 1847,
"cdna_end": null,
"cdna_length": 2565,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1364T>G",
"hgvs_p": "p.Leu455Arg",
"transcript": "ENST00000423167.6",
"protein_id": "ENSP00000413012.2",
"transcript_support_level": 1,
"aa_start": 455,
"aa_end": null,
"aa_length": 658,
"cds_start": 1364,
"cds_end": null,
"cds_length": 1977,
"cdna_start": 1549,
"cdna_end": null,
"cdna_length": 2776,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1508T>G",
"hgvs_p": "p.Leu503Arg",
"transcript": "NM_001199042.2",
"protein_id": "NP_001185971.1",
"transcript_support_level": null,
"aa_start": 503,
"aa_end": null,
"aa_length": 706,
"cds_start": 1508,
"cds_end": null,
"cds_length": 2121,
"cdna_start": 1776,
"cdna_end": null,
"cdna_length": 3003,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1502T>G",
"hgvs_p": "p.Leu501Arg",
"transcript": "NM_001199040.2",
"protein_id": "NP_001185969.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 704,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2115,
"cdna_start": 1753,
"cdna_end": null,
"cdna_length": 2980,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1502T>G",
"hgvs_p": "p.Leu501Arg",
"transcript": "ENST00000535552.5",
"protein_id": "ENSP00000440238.1",
"transcript_support_level": 2,
"aa_start": 501,
"aa_end": null,
"aa_length": 704,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2115,
"cdna_start": 1753,
"cdna_end": null,
"cdna_length": 2631,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1436T>G",
"hgvs_p": "p.Leu479Arg",
"transcript": "NM_001199041.2",
"protein_id": "NP_001185970.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 682,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2049,
"cdna_start": 1764,
"cdna_end": null,
"cdna_length": 2991,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1436T>G",
"hgvs_p": "p.Leu479Arg",
"transcript": "ENST00000574278.5",
"protein_id": "ENSP00000458827.1",
"transcript_support_level": 2,
"aa_start": 479,
"aa_end": null,
"aa_length": 682,
"cds_start": 1436,
"cds_end": null,
"cds_length": 2049,
"cdna_start": 1764,
"cdna_end": null,
"cdna_length": 2455,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "NM_001142617.2",
"protein_id": "NP_001136089.1",
"transcript_support_level": null,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1596,
"cdna_end": null,
"cdna_length": 2823,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "NM_001142618.2",
"protein_id": "NP_001136090.1",
"transcript_support_level": null,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1461,
"cdna_end": null,
"cdna_length": 2688,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "NM_001437994.1",
"protein_id": "NP_001424923.1",
"transcript_support_level": null,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1539,
"cdna_end": null,
"cdna_length": 2766,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "ENST00000323940.9",
"protein_id": "ENSP00000326085.5",
"transcript_support_level": 2,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1637,
"cdna_end": null,
"cdna_length": 2864,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "ENST00000449139.6",
"protein_id": "ENSP00000410221.2",
"transcript_support_level": 5,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1505,
"cdna_end": null,
"cdna_length": 2732,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "ENST00000616000.4",
"protein_id": "ENSP00000479112.1",
"transcript_support_level": 2,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1619,
"cdna_end": null,
"cdna_length": 2843,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1367T>G",
"hgvs_p": "p.Leu456Arg",
"transcript": "ENST00000416286.7",
"protein_id": "ENSP00000400403.3",
"transcript_support_level": 5,
"aa_start": 456,
"aa_end": null,
"aa_length": 659,
"cds_start": 1367,
"cds_end": null,
"cds_length": 1980,
"cdna_start": 1523,
"cdna_end": null,
"cdna_length": 2750,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1364T>G",
"hgvs_p": "p.Leu455Arg",
"transcript": "NM_001142619.2",
"protein_id": "NP_001136091.1",
"transcript_support_level": null,
"aa_start": 455,
"aa_end": null,
"aa_length": 658,
"cds_start": 1364,
"cds_end": null,
"cds_length": 1977,
"cdna_start": 1569,
"cdna_end": null,
"cdna_length": 2796,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1439T>G",
"hgvs_p": "p.Leu480Arg",
"transcript": "XM_017022478.2",
"protein_id": "XP_016877967.1",
"transcript_support_level": null,
"aa_start": 480,
"aa_end": null,
"aa_length": 683,
"cds_start": 1439,
"cds_end": null,
"cds_length": 2052,
"cdna_start": 1808,
"cdna_end": null,
"cdna_length": 3035,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg",
"transcript": "XM_017022479.2",
"protein_id": "XP_016877968.1",
"transcript_support_level": null,
"aa_start": 464,
"aa_end": null,
"aa_length": 667,
"cds_start": 1391,
"cds_end": null,
"cds_length": 2004,
"cdna_start": 1571,
"cdna_end": null,
"cdna_length": 2798,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "c.285T>G",
"hgvs_p": "p.Pro95Pro",
"transcript": "ENST00000572785.1",
"protein_id": "ENSP00000459546.1",
"transcript_support_level": 3,
"aa_start": 95,
"aa_end": null,
"aa_length": 264,
"cds_start": 285,
"cds_end": null,
"cds_length": 796,
"cdna_start": 286,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "n.1100T>G",
"hgvs_p": null,
"transcript": "ENST00000545137.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2324,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "n.1663T>G",
"hgvs_p": null,
"transcript": "ENST00000574439.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2887,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "n.509T>G",
"hgvs_p": null,
"transcript": "ENST00000575272.1",
"protein_id": null,
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 572,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "n.1776T>G",
"hgvs_p": null,
"transcript": "XR_931877.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1884,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"hgvs_c": "n.*690T>G",
"hgvs_p": null,
"transcript": "ENST00000569936.5",
"protein_id": "ENSP00000461799.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2151,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "STRA6",
"gene_hgnc_id": 30650,
"dbsnp": "rs201408425",
"frequency_reference_population": 0.00015303328,
"hom_count_reference_population": 4,
"allele_count_reference_population": 247,
"gnomad_exomes_af": 0.000146402,
"gnomad_genomes_af": 0.000216672,
"gnomad_exomes_ac": 214,
"gnomad_genomes_ac": 33,
"gnomad_exomes_homalt": 3,
"gnomad_genomes_homalt": 1,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.06258991360664368,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.713,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.1427,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.07,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 4.134,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.01,
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000395105.9",
"gene_symbol": "STRA6",
"hgnc_id": 30650,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.1391T>G",
"hgvs_p": "p.Leu464Arg"
}
],
"clinvar_disease": "Matthew-Wood syndrome,not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2",
"phenotype_combined": "Matthew-Wood syndrome|not provided",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}