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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: 3-33510667-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=33510667&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 33510667,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001365628.1",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4208A>G",
"hgvs_p": "p.Asp1403Gly",
"transcript": "NM_001365631.1",
"protein_id": "NP_001352560.1",
"transcript_support_level": null,
"aa_start": 1403,
"aa_end": null,
"aa_length": 1506,
"cds_start": 4208,
"cds_end": null,
"cds_length": 4521,
"cdna_start": 4460,
"cdna_end": null,
"cdna_length": 7159,
"mane_select": "ENST00000682230.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365631.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4208A>G",
"hgvs_p": "p.Asp1403Gly",
"transcript": "ENST00000682230.1",
"protein_id": "ENSP00000507498.1",
"transcript_support_level": null,
"aa_start": 1403,
"aa_end": null,
"aa_length": 1506,
"cds_start": 4208,
"cds_end": null,
"cds_length": 4521,
"cdna_start": 4460,
"cdna_end": null,
"cdna_length": 7159,
"mane_select": "NM_001365631.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000682230.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 38,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4295A>G",
"hgvs_p": "p.Asp1432Gly",
"transcript": "NM_001365628.1",
"protein_id": "NP_001352557.1",
"transcript_support_level": null,
"aa_start": 1432,
"aa_end": null,
"aa_length": 1535,
"cds_start": 4295,
"cds_end": null,
"cds_length": 4608,
"cdna_start": 4547,
"cdna_end": null,
"cdna_length": 7246,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365628.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 38,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4292A>G",
"hgvs_p": "p.Asp1431Gly",
"transcript": "NM_001365629.1",
"protein_id": "NP_001352558.1",
"transcript_support_level": null,
"aa_start": 1431,
"aa_end": null,
"aa_length": 1534,
"cds_start": 4292,
"cds_end": null,
"cds_length": 4605,
"cdna_start": 4544,
"cdna_end": null,
"cdna_length": 7243,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365629.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 38,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4271A>G",
"hgvs_p": "p.Asp1424Gly",
"transcript": "NM_001365627.1",
"protein_id": "NP_001352556.1",
"transcript_support_level": null,
"aa_start": 1424,
"aa_end": null,
"aa_length": 1527,
"cds_start": 4271,
"cds_end": null,
"cds_length": 4584,
"cdna_start": 4523,
"cdna_end": null,
"cdna_length": 7222,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365627.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4268A>G",
"hgvs_p": "p.Asp1423Gly",
"transcript": "NM_001375694.1",
"protein_id": "NP_001362623.1",
"transcript_support_level": null,
"aa_start": 1423,
"aa_end": null,
"aa_length": 1526,
"cds_start": 4268,
"cds_end": null,
"cds_length": 4581,
"cdna_start": 4520,
"cdna_end": null,
"cdna_length": 7219,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375694.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4244A>G",
"hgvs_p": "p.Asp1415Gly",
"transcript": "NM_001375697.1",
"protein_id": "NP_001362626.1",
"transcript_support_level": null,
"aa_start": 1415,
"aa_end": null,
"aa_length": 1518,
"cds_start": 4244,
"cds_end": null,
"cds_length": 4557,
"cdna_start": 4496,
"cdna_end": null,
"cdna_length": 7195,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375697.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 38,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4235A>G",
"hgvs_p": "p.Asp1412Gly",
"transcript": "NM_015097.3",
"protein_id": "NP_055912.2",
"transcript_support_level": null,
"aa_start": 1412,
"aa_end": null,
"aa_length": 1515,
"cds_start": 4235,
"cds_end": null,
"cds_length": 4548,
"cdna_start": 4487,
"cdna_end": null,
"cdna_length": 7186,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015097.3"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4232A>G",
"hgvs_p": "p.Asp1411Gly",
"transcript": "NM_001375700.1",
"protein_id": "NP_001362629.1",
"transcript_support_level": null,
"aa_start": 1411,
"aa_end": null,
"aa_length": 1514,
"cds_start": 4232,
"cds_end": null,
"cds_length": 4545,
"cdna_start": 4484,
"cdna_end": null,
"cdna_length": 7183,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375700.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4232A>G",
"hgvs_p": "p.Asp1411Gly",
"transcript": "NM_001375701.1",
"protein_id": "NP_001362630.1",
"transcript_support_level": null,
"aa_start": 1411,
"aa_end": null,
"aa_length": 1514,
"cds_start": 4232,
"cds_end": null,
"cds_length": 4545,
"cdna_start": 4484,
"cdna_end": null,
"cdna_length": 7183,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375701.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4232A>G",
"hgvs_p": "p.Asp1411Gly",
"transcript": "ENST00000468888.6",
"protein_id": "ENSP00000419974.2",
"transcript_support_level": 5,
"aa_start": 1411,
"aa_end": null,
"aa_length": 1514,
"cds_start": 4232,
"cds_end": null,
"cds_length": 4545,
"cdna_start": 4279,
"cdna_end": null,
"cdna_length": 6978,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000468888.6"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4229A>G",
"hgvs_p": "p.Asp1410Gly",
"transcript": "ENST00000399362.8",
"protein_id": "ENSP00000382297.4",
"transcript_support_level": 5,
"aa_start": 1410,
"aa_end": null,
"aa_length": 1513,
"cds_start": 4229,
"cds_end": null,
"cds_length": 4542,
"cdna_start": 4583,
"cdna_end": null,
"cdna_length": 7282,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000399362.8"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4217A>G",
"hgvs_p": "p.Asp1406Gly",
"transcript": "NM_001365630.1",
"protein_id": "NP_001352559.1",
"transcript_support_level": null,
"aa_start": 1406,
"aa_end": null,
"aa_length": 1509,
"cds_start": 4217,
"cds_end": null,
"cds_length": 4530,
"cdna_start": 4469,
"cdna_end": null,
"cdna_length": 7168,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365630.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4214A>G",
"hgvs_p": "p.Asp1405Gly",
"transcript": "NM_001375705.1",
"protein_id": "NP_001362634.1",
"transcript_support_level": null,
"aa_start": 1405,
"aa_end": null,
"aa_length": 1508,
"cds_start": 4214,
"cds_end": null,
"cds_length": 4527,
"cdna_start": 4466,
"cdna_end": null,
"cdna_length": 7165,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375705.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4208A>G",
"hgvs_p": "p.Asp1403Gly",
"transcript": "NM_001400405.1",
"protein_id": "NP_001387334.1",
"transcript_support_level": null,
"aa_start": 1403,
"aa_end": null,
"aa_length": 1506,
"cds_start": 4208,
"cds_end": null,
"cds_length": 4521,
"cdna_start": 4460,
"cdna_end": null,
"cdna_length": 7159,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001400405.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4205A>G",
"hgvs_p": "p.Asp1402Gly",
"transcript": "NM_001365632.1",
"protein_id": "NP_001352561.1",
"transcript_support_level": null,
"aa_start": 1402,
"aa_end": null,
"aa_length": 1505,
"cds_start": 4205,
"cds_end": null,
"cds_length": 4518,
"cdna_start": 4457,
"cdna_end": null,
"cdna_length": 7156,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365632.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4205A>G",
"hgvs_p": "p.Asp1402Gly",
"transcript": "ENST00000912539.1",
"protein_id": "ENSP00000582598.1",
"transcript_support_level": null,
"aa_start": 1402,
"aa_end": null,
"aa_length": 1505,
"cds_start": 4205,
"cds_end": null,
"cds_length": 4518,
"cdna_start": 4457,
"cdna_end": null,
"cdna_length": 7151,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912539.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4184A>G",
"hgvs_p": "p.Asp1395Gly",
"transcript": "ENST00000912540.1",
"protein_id": "ENSP00000582599.1",
"transcript_support_level": null,
"aa_start": 1395,
"aa_end": null,
"aa_length": 1498,
"cds_start": 4184,
"cds_end": null,
"cds_length": 4497,
"cdna_start": 4394,
"cdna_end": null,
"cdna_length": 6347,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912540.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4169A>G",
"hgvs_p": "p.Asp1390Gly",
"transcript": "NM_001365633.1",
"protein_id": "NP_001352562.1",
"transcript_support_level": null,
"aa_start": 1390,
"aa_end": null,
"aa_length": 1493,
"cds_start": 4169,
"cds_end": null,
"cds_length": 4482,
"cdna_start": 4421,
"cdna_end": null,
"cdna_length": 7120,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365633.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4166A>G",
"hgvs_p": "p.Asp1389Gly",
"transcript": "NM_001365634.1",
"protein_id": "NP_001352563.1",
"transcript_support_level": null,
"aa_start": 1389,
"aa_end": null,
"aa_length": 1492,
"cds_start": 4166,
"cds_end": null,
"cds_length": 4479,
"cdna_start": 4418,
"cdna_end": null,
"cdna_length": 7117,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365634.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4166A>G",
"hgvs_p": "p.Asp1389Gly",
"transcript": "NM_001375703.1",
"protein_id": "NP_001362632.1",
"transcript_support_level": null,
"aa_start": 1389,
"aa_end": null,
"aa_length": 1492,
"cds_start": 4166,
"cds_end": null,
"cds_length": 4479,
"cdna_start": 4418,
"cdna_end": null,
"cdna_length": 7117,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375703.1"
},
{
"aa_ref": "D",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CLASP2",
"gene_hgnc_id": 17078,
"hgvs_c": "c.4166A>G",
"hgvs_p": "p.Asp1389Gly",
"transcript": "ENST00000895686.1",
"protein_id": "ENSP00000565745.1",
"transcript_support_level": null,
"aa_start": 1389,
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{
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{
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{
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{
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{
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],
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{
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],
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000476251.1"
},
{
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"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
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"gene_symbol": "CLASP2",
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"biotype": "nonsense_mediated_decay",
"feature": "ENST00000476251.1"
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],
"gene_symbol": "CLASP2",
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"dbsnp": "rs953040113",
"frequency_reference_population": 0.00003346243,
"hom_count_reference_population": 0,
"allele_count_reference_population": 54,
"gnomad_exomes_af": 0.0000321566,
"gnomad_genomes_af": 0.000046006,
"gnomad_exomes_ac": 47,
"gnomad_genomes_ac": 7,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5221386551856995,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.551,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.6084,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.02,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 5.867,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.02,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BS2",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_001365628.1",
"gene_symbol": "CLASP2",
"hgnc_id": 17078,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.4295A>G",
"hgvs_p": "p.Asp1432Gly"
}
],
"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
}