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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: 2-63913259-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=63913259&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 63913259,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_016516.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "NM_016516.3",
"protein_id": "NP_057600.2",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000272322.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016516.3"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "ENST00000272322.9",
"protein_id": "ENSP00000272322.4",
"transcript_support_level": 5,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_016516.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000272322.9"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2350G>A",
"hgvs_p": "p.Val784Ile",
"transcript": "ENST00000409558.8",
"protein_id": "ENSP00000386980.3",
"transcript_support_level": 1,
"aa_start": 784,
"aa_end": null,
"aa_length": 965,
"cds_start": 2350,
"cds_end": null,
"cds_length": 2898,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409558.8"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.1927G>A",
"hgvs_p": "p.Val643Ile",
"transcript": "ENST00000354504.7",
"protein_id": "ENSP00000346499.3",
"transcript_support_level": 1,
"aa_start": 643,
"aa_end": null,
"aa_length": 824,
"cds_start": 1927,
"cds_end": null,
"cds_length": 2475,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000354504.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "n.*126G>A",
"hgvs_p": null,
"transcript": "ENST00000416400.1",
"protein_id": "ENSP00000414725.2",
"transcript_support_level": 1,
"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": "ENST00000416400.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "n.*126G>A",
"hgvs_p": null,
"transcript": "ENST00000416400.1",
"protein_id": "ENSP00000414725.2",
"transcript_support_level": 1,
"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": "ENST00000416400.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2410G>A",
"hgvs_p": "p.Val804Ile",
"transcript": "ENST00000949097.1",
"protein_id": "ENSP00000619156.1",
"transcript_support_level": null,
"aa_start": 804,
"aa_end": null,
"aa_length": 985,
"cds_start": 2410,
"cds_end": null,
"cds_length": 2958,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949097.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "ENST00000949098.1",
"protein_id": "ENSP00000619157.1",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949098.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "ENST00000949099.1",
"protein_id": "ENSP00000619158.1",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949099.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2380G>A",
"hgvs_p": "p.Val794Ile",
"transcript": "ENST00000949096.1",
"protein_id": "ENSP00000619155.1",
"transcript_support_level": null,
"aa_start": 794,
"aa_end": null,
"aa_length": 975,
"cds_start": 2380,
"cds_end": null,
"cds_length": 2928,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949096.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2350G>A",
"hgvs_p": "p.Val784Ile",
"transcript": "NM_001005739.2",
"protein_id": "NP_001005739.1",
"transcript_support_level": null,
"aa_start": 784,
"aa_end": null,
"aa_length": 965,
"cds_start": 2350,
"cds_end": null,
"cds_length": 2898,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001005739.2"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2350G>A",
"hgvs_p": "p.Val784Ile",
"transcript": "ENST00000851817.1",
"protein_id": "ENSP00000521876.1",
"transcript_support_level": null,
"aa_start": 784,
"aa_end": null,
"aa_length": 965,
"cds_start": 2350,
"cds_end": null,
"cds_length": 2898,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851817.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2344G>A",
"hgvs_p": "p.Val782Ile",
"transcript": "ENST00000851818.1",
"protein_id": "ENSP00000521877.1",
"transcript_support_level": null,
"aa_start": 782,
"aa_end": null,
"aa_length": 963,
"cds_start": 2344,
"cds_end": null,
"cds_length": 2892,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851818.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "ENST00000922500.1",
"protein_id": "ENSP00000592559.1",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 950,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2853,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000922500.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2278G>A",
"hgvs_p": "p.Val760Ile",
"transcript": "ENST00000922499.1",
"protein_id": "ENSP00000592558.1",
"transcript_support_level": null,
"aa_start": 760,
"aa_end": null,
"aa_length": 941,
"cds_start": 2278,
"cds_end": null,
"cds_length": 2826,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000922499.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2350G>A",
"hgvs_p": "p.Val784Ile",
"transcript": "ENST00000949095.1",
"protein_id": "ENSP00000619154.1",
"transcript_support_level": null,
"aa_start": 784,
"aa_end": null,
"aa_length": 938,
"cds_start": 2350,
"cds_end": null,
"cds_length": 2817,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949095.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2242G>A",
"hgvs_p": "p.Val748Ile",
"transcript": "ENST00000851816.1",
"protein_id": "ENSP00000521875.1",
"transcript_support_level": null,
"aa_start": 748,
"aa_end": null,
"aa_length": 929,
"cds_start": 2242,
"cds_end": null,
"cds_length": 2790,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000851816.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "XM_047444727.1",
"protein_id": "XP_047300683.1",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047444727.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile",
"transcript": "XM_047444728.1",
"protein_id": "XP_047300684.1",
"transcript_support_level": null,
"aa_start": 796,
"aa_end": null,
"aa_length": 977,
"cds_start": 2386,
"cds_end": null,
"cds_length": 2934,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047444728.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2350G>A",
"hgvs_p": "p.Val784Ile",
"transcript": "XM_047444729.1",
"protein_id": "XP_047300685.1",
"transcript_support_level": null,
"aa_start": 784,
"aa_end": null,
"aa_length": 965,
"cds_start": 2350,
"cds_end": null,
"cds_length": 2898,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047444729.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2032G>A",
"hgvs_p": "p.Val678Ile",
"transcript": "XM_017004316.2",
"protein_id": "XP_016859805.1",
"transcript_support_level": null,
"aa_start": 678,
"aa_end": null,
"aa_length": 859,
"cds_start": 2032,
"cds_end": null,
"cds_length": 2580,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017004316.2"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VPS54",
"gene_hgnc_id": 18652,
"hgvs_c": "c.2032G>A",
"hgvs_p": "p.Val678Ile",
"transcript": "XM_047444730.1",
"protein_id": "XP_047300686.1",
"transcript_support_level": null,
"aa_start": 678,
"aa_end": null,
"aa_length": 859,
"cds_start": 2032,
"cds_end": null,
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"biotype": "protein_coding",
"feature": "XM_047444730.1"
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{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 19,
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"exon_count": 19,
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"intron_rank_end": null,
"gene_symbol": "VPS54",
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"hgvs_c": "n.2998G>A",
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"transcript": "XR_007076389.1",
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"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_007076389.1"
}
],
"gene_symbol": "VPS54",
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"dbsnp": "rs776252599",
"frequency_reference_population": 6.8546206e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.85462e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.2325255274772644,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.20000000298023224,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.221,
"revel_prediction": "Benign",
"alphamissense_score": 0.1153,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.33,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.879,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.2,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_016516.3",
"gene_symbol": "VPS54",
"hgnc_id": 18652,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.2386G>A",
"hgvs_p": "p.Val796Ile"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}