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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: 7-77330303-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=77330303&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 77330303,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_017439.4",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1610A>G",
"hgvs_p": "p.Lys537Arg",
"transcript": "NM_017439.4",
"protein_id": "NP_059135.2",
"transcript_support_level": null,
"aa_start": 537,
"aa_end": null,
"aa_length": 854,
"cds_start": 1610,
"cds_end": null,
"cds_length": 2565,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000257626.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017439.4"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1610A>G",
"hgvs_p": "p.Lys537Arg",
"transcript": "ENST00000257626.12",
"protein_id": "ENSP00000257626.7",
"transcript_support_level": 1,
"aa_start": 537,
"aa_end": null,
"aa_length": 854,
"cds_start": 1610,
"cds_end": null,
"cds_length": 2565,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_017439.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000257626.12"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1610A>G",
"hgvs_p": "p.Lys537Arg",
"transcript": "NM_001350896.2",
"protein_id": "NP_001337825.1",
"transcript_support_level": null,
"aa_start": 537,
"aa_end": null,
"aa_length": 854,
"cds_start": 1610,
"cds_end": null,
"cds_length": 2565,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350896.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1664A>G",
"hgvs_p": "p.Lys555Arg",
"transcript": "ENST00000943097.1",
"protein_id": "ENSP00000613156.1",
"transcript_support_level": null,
"aa_start": 555,
"aa_end": null,
"aa_length": 838,
"cds_start": 1664,
"cds_end": null,
"cds_length": 2517,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943097.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1556A>G",
"hgvs_p": "p.Lys519Arg",
"transcript": "NM_001350897.2",
"protein_id": "NP_001337826.1",
"transcript_support_level": null,
"aa_start": 519,
"aa_end": null,
"aa_length": 836,
"cds_start": 1556,
"cds_end": null,
"cds_length": 2511,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350897.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1553A>G",
"hgvs_p": "p.Lys518Arg",
"transcript": "NM_001350898.2",
"protein_id": "NP_001337827.1",
"transcript_support_level": null,
"aa_start": 518,
"aa_end": null,
"aa_length": 835,
"cds_start": 1553,
"cds_end": null,
"cds_length": 2508,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350898.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1610A>G",
"hgvs_p": "p.Lys537Arg",
"transcript": "ENST00000880888.1",
"protein_id": "ENSP00000550947.1",
"transcript_support_level": null,
"aa_start": 537,
"aa_end": null,
"aa_length": 820,
"cds_start": 1610,
"cds_end": null,
"cds_length": 2463,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000880888.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1610A>G",
"hgvs_p": "p.Lys537Arg",
"transcript": "NM_001350899.2",
"protein_id": "NP_001337828.1",
"transcript_support_level": null,
"aa_start": 537,
"aa_end": null,
"aa_length": 806,
"cds_start": 1610,
"cds_end": null,
"cds_length": 2421,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350899.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.965A>G",
"hgvs_p": "p.Lys322Arg",
"transcript": "NM_001350900.2",
"protein_id": "NP_001337829.1",
"transcript_support_level": null,
"aa_start": 322,
"aa_end": null,
"aa_length": 639,
"cds_start": 965,
"cds_end": null,
"cds_length": 1920,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350900.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.965A>G",
"hgvs_p": "p.Lys322Arg",
"transcript": "NM_001350901.2",
"protein_id": "NP_001337830.1",
"transcript_support_level": null,
"aa_start": 322,
"aa_end": null,
"aa_length": 607,
"cds_start": 965,
"cds_end": null,
"cds_length": 1824,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350901.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.65A>G",
"hgvs_p": "p.Lys22Arg",
"transcript": "ENST00000415112.2",
"protein_id": "ENSP00000396230.2",
"transcript_support_level": 3,
"aa_start": 22,
"aa_end": null,
"aa_length": 187,
"cds_start": 65,
"cds_end": null,
"cds_length": 564,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000415112.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1664A>G",
"hgvs_p": "p.Lys555Arg",
"transcript": "XM_011516325.3",
"protein_id": "XP_011514627.1",
"transcript_support_level": null,
"aa_start": 555,
"aa_end": null,
"aa_length": 872,
"cds_start": 1664,
"cds_end": null,
"cds_length": 2619,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011516325.3"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1664A>G",
"hgvs_p": "p.Lys555Arg",
"transcript": "XM_011516327.3",
"protein_id": "XP_011514629.1",
"transcript_support_level": null,
"aa_start": 555,
"aa_end": null,
"aa_length": 824,
"cds_start": 1664,
"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": "XM_011516327.3"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1556A>G",
"hgvs_p": "p.Lys519Arg",
"transcript": "XM_047420487.1",
"protein_id": "XP_047276443.1",
"transcript_support_level": null,
"aa_start": 519,
"aa_end": null,
"aa_length": 788,
"cds_start": 1556,
"cds_end": null,
"cds_length": 2367,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420487.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1664A>G",
"hgvs_p": "p.Lys555Arg",
"transcript": "XM_047420488.1",
"protein_id": "XP_047276444.1",
"transcript_support_level": null,
"aa_start": 555,
"aa_end": null,
"aa_length": 723,
"cds_start": 1664,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420488.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1664A>G",
"hgvs_p": "p.Lys555Arg",
"transcript": "XM_047420489.1",
"protein_id": "XP_047276445.1",
"transcript_support_level": null,
"aa_start": 555,
"aa_end": null,
"aa_length": 718,
"cds_start": 1664,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420489.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1019A>G",
"hgvs_p": "p.Lys340Arg",
"transcript": "XM_011516330.3",
"protein_id": "XP_011514632.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 657,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011516330.3"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1019A>G",
"hgvs_p": "p.Lys340Arg",
"transcript": "XM_017012346.2",
"protein_id": "XP_016867835.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 657,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017012346.2"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1019A>G",
"hgvs_p": "p.Lys340Arg",
"transcript": "XM_047420490.1",
"protein_id": "XP_047276446.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 657,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420490.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1019A>G",
"hgvs_p": "p.Lys340Arg",
"transcript": "XM_047420491.1",
"protein_id": "XP_047276447.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 657,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420491.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.1019A>G",
"hgvs_p": "p.Lys340Arg",
"transcript": "XM_047420492.1",
"protein_id": "XP_047276448.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 657,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1974,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047420492.1"
},
{
"aa_ref": "K",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GSAP",
"gene_hgnc_id": 28042,
"hgvs_c": "c.965A>G",
"hgvs_p": "p.Lys322Arg",
"transcript": "XM_047420493.1",
"protein_id": "XP_047276449.1",
"transcript_support_level": null,
"aa_start": 322,
"aa_end": null,
"aa_length": 639,
"cds_start": 965,
"cds_end": null,
"cds_length": 1920,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
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"splice_prediction_selected": "Benign",
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"bayesdelnoaf_prediction": "Benign",
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"phylop100way_prediction": "Benign",
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{
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],
"verdict": "Uncertain_significance",
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],
"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
}