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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: 7-94598851-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=94598851&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 94598851,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000648936.2",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1177G>A",
"hgvs_p": "p.Val393Met",
"transcript": "NM_003919.3",
"protein_id": "NP_003910.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 437,
"cds_start": 1177,
"cds_end": null,
"cds_length": 1314,
"cdna_start": 1212,
"cdna_end": null,
"cdna_length": 1868,
"mane_select": "ENST00000648936.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1177G>A",
"hgvs_p": "p.Val393Met",
"transcript": "ENST00000648936.2",
"protein_id": "ENSP00000497130.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 437,
"cds_start": 1177,
"cds_end": null,
"cds_length": 1314,
"cdna_start": 1212,
"cdna_end": null,
"cdna_length": 1868,
"mane_select": "NM_003919.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1129G>A",
"hgvs_p": "p.Val377Met",
"transcript": "ENST00000428696.7",
"protein_id": "ENSP00000397536.3",
"transcript_support_level": 1,
"aa_start": 377,
"aa_end": null,
"aa_length": 444,
"cds_start": 1129,
"cds_end": null,
"cds_length": 1335,
"cdna_start": 1136,
"cdna_end": null,
"cdna_length": 1368,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1150G>A",
"hgvs_p": "p.Val384Met",
"transcript": "ENST00000447873.6",
"protein_id": "ENSP00000388734.1",
"transcript_support_level": 1,
"aa_start": 384,
"aa_end": null,
"aa_length": 428,
"cds_start": 1150,
"cds_end": null,
"cds_length": 1287,
"cdna_start": 1259,
"cdna_end": null,
"cdna_length": 1672,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Val429Met",
"transcript": "ENST00000647096.1",
"protein_id": "ENSP00000494192.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 500,
"cds_start": 1285,
"cds_end": null,
"cds_length": 1503,
"cdna_start": 1303,
"cdna_end": null,
"cdna_length": 1610,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1339G>A",
"hgvs_p": "p.Val447Met",
"transcript": "ENST00000645101.1",
"protein_id": "ENSP00000494975.1",
"transcript_support_level": null,
"aa_start": 447,
"aa_end": null,
"aa_length": 491,
"cds_start": 1339,
"cds_end": null,
"cds_length": 1476,
"cdna_start": 1387,
"cdna_end": null,
"cdna_length": 1739,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "ENST00000642707.1",
"protein_id": "ENSP00000495270.1",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
"aa_length": 489,
"cds_start": 1258,
"cds_end": null,
"cds_length": 1470,
"cdna_start": 1296,
"cdna_end": null,
"cdna_length": 1713,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "ENST00000647351.1",
"protein_id": "ENSP00000494556.1",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
"aa_length": 487,
"cds_start": 1258,
"cds_end": null,
"cds_length": 1464,
"cdna_start": 1286,
"cdna_end": null,
"cdna_length": 1977,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1177G>A",
"hgvs_p": "p.Val393Met",
"transcript": "ENST00000646943.1",
"protein_id": "ENSP00000494666.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 485,
"cds_start": 1177,
"cds_end": null,
"cds_length": 1458,
"cdna_start": 1205,
"cdna_end": null,
"cdna_length": 1667,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "ENST00000644122.1",
"protein_id": "ENSP00000495236.1",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
"aa_length": 482,
"cds_start": 1258,
"cds_end": null,
"cds_length": 1449,
"cdna_start": 1365,
"cdna_end": null,
"cdna_length": 1779,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1255G>A",
"hgvs_p": "p.Val419Met",
"transcript": "ENST00000647334.1",
"protein_id": "ENSP00000495114.1",
"transcript_support_level": null,
"aa_start": 419,
"aa_end": null,
"aa_length": 481,
"cds_start": 1255,
"cds_end": null,
"cds_length": 1446,
"cdna_start": 1256,
"cdna_end": null,
"cdna_length": 1554,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1237G>A",
"hgvs_p": "p.Val413Met",
"transcript": "ENST00000646265.1",
"protein_id": "ENSP00000494587.1",
"transcript_support_level": null,
"aa_start": 413,
"aa_end": null,
"aa_length": 480,
"cds_start": 1237,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1239,
"cdna_end": null,
"cdna_length": 1564,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1231G>A",
"hgvs_p": "p.Val411Met",
"transcript": "ENST00000642441.1",
"protein_id": "ENSP00000495994.1",
"transcript_support_level": null,
"aa_start": 411,
"aa_end": null,
"aa_length": 478,
"cds_start": 1231,
"cds_end": null,
"cds_length": 1437,
"cdna_start": 1282,
"cdna_end": null,
"cdna_length": 1592,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
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"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1150G>A",
"hgvs_p": "p.Val384Met",
"transcript": "ENST00000644116.1",
"protein_id": "ENSP00000495276.1",
"transcript_support_level": null,
"aa_start": 384,
"aa_end": null,
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"cds_start": 1150,
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"cdna_start": 1199,
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 10,
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"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Val429Met",
"transcript": "NM_001346713.2",
"protein_id": "NP_001333642.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 473,
"cds_start": 1285,
"cds_end": null,
"cds_length": 1422,
"cdna_start": 1320,
"cdna_end": null,
"cdna_length": 1976,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1216G>A",
"hgvs_p": "p.Val406Met",
"transcript": "ENST00000644375.1",
"protein_id": "ENSP00000494315.1",
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"aa_start": 406,
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"mane_select": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 10,
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"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Val429Met",
"transcript": "ENST00000646489.1",
"protein_id": "ENSP00000496268.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 473,
"cds_start": 1285,
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"cdna_start": 1327,
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"cdna_length": 1733,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Val429Met",
"transcript": "ENST00000415788.3",
"protein_id": "ENSP00000405313.2",
"transcript_support_level": 2,
"aa_start": 429,
"aa_end": null,
"aa_length": 471,
"cds_start": 1285,
"cds_end": null,
"cds_length": 1416,
"cdna_start": 1373,
"cdna_end": null,
"cdna_length": 1979,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
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"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "NM_001346715.2",
"protein_id": "NP_001333644.1",
"transcript_support_level": null,
"aa_start": 420,
"aa_end": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "ENST00000643272.1",
"protein_id": "ENSP00000494488.1",
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"aa_start": 420,
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"aa_length": 464,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": 10,
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"exon_count": 12,
"intron_rank": null,
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"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1258G>A",
"hgvs_p": "p.Val420Met",
"transcript": "ENST00000644551.1",
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"aa_length": 464,
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"cdna_start": 1346,
"cdna_end": null,
"cdna_length": 1713,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1177G>A",
"hgvs_p": "p.Val393Met",
"transcript": "NM_001099401.2",
"protein_id": "NP_001092871.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 462,
"cds_start": 1177,
"cds_end": null,
"cds_length": 1389,
"cdna_start": 1212,
"cdna_end": null,
"cdna_length": 1943,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SGCE",
"gene_hgnc_id": 10808,
"hgvs_c": "c.1177G>A",
"hgvs_p": "p.Val393Met",
"transcript": "ENST00000445866.7",
"protein_id": "ENSP00000398930.2",
"transcript_support_level": 5,
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],
"clinvar_disease": "Inborn genetic diseases,Myoclonic dystonia 11",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "Myoclonic dystonia 11|Inborn genetic diseases",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}