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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: 22-24096051-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=24096051&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 24096051,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000263119.10",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "NM_012295.4",
"protein_id": "NP_036427.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2220,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6663,
"cdna_start": 4045,
"cdna_end": null,
"cdna_length": 7233,
"mane_select": "ENST00000263119.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "ENST00000263119.10",
"protein_id": "ENSP00000263119.5",
"transcript_support_level": 1,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2220,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6663,
"cdna_start": 4045,
"cdna_end": null,
"cdna_length": 7233,
"mane_select": "NM_012295.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "ENST00000398319.6",
"protein_id": "ENSP00000381364.2",
"transcript_support_level": 1,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2220,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6663,
"cdna_start": 4292,
"cdna_end": null,
"cdna_length": 7480,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3757G>A",
"hgvs_p": "p.Glu1253Lys",
"transcript": "ENST00000405822.6",
"protein_id": "ENSP00000384694.2",
"transcript_support_level": 1,
"aa_start": 1253,
"aa_end": null,
"aa_length": 2141,
"cds_start": 3757,
"cds_end": null,
"cds_length": 6426,
"cdna_start": 3851,
"cdna_end": null,
"cdna_length": 6952,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "NM_001199281.1",
"protein_id": "NP_001186210.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2220,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6663,
"cdna_start": 4340,
"cdna_end": null,
"cdna_length": 7528,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3757G>A",
"hgvs_p": "p.Glu1253Lys",
"transcript": "NM_001201429.2",
"protein_id": "NP_001188358.1",
"transcript_support_level": null,
"aa_start": 1253,
"aa_end": null,
"aa_length": 2170,
"cds_start": 3757,
"cds_end": null,
"cds_length": 6513,
"cdna_start": 3895,
"cdna_end": null,
"cdna_length": 7083,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3757G>A",
"hgvs_p": "p.Glu1253Lys",
"transcript": "ENST00000617531.4",
"protein_id": "ENSP00000480560.1",
"transcript_support_level": 5,
"aa_start": 1253,
"aa_end": null,
"aa_length": 2170,
"cds_start": 3757,
"cds_end": null,
"cds_length": 6513,
"cdna_start": 3884,
"cdna_end": null,
"cdna_length": 7072,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_005261415.4",
"protein_id": "XP_005261472.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2255,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6768,
"cdna_start": 4340,
"cdna_end": null,
"cdna_length": 7633,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_024452184.2",
"protein_id": "XP_024307952.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2255,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6768,
"cdna_start": 4045,
"cdna_end": null,
"cdna_length": 7338,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_005261416.4",
"protein_id": "XP_005261473.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2250,
"cds_start": 3907,
"cds_end": null,
"cds_length": 6753,
"cdna_start": 4340,
"cdna_end": null,
"cdna_length": 7618,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_006724179.3",
"protein_id": "XP_006724242.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
"aa_length": 2226,
"cds_start": 3907,
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"cds_length": 6681,
"cdna_start": 4340,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_005261417.4",
"protein_id": "XP_005261474.1",
"transcript_support_level": null,
"aa_start": 1303,
"aa_end": null,
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"cds_start": 3907,
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"cdna_start": 4340,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_047441217.1",
"protein_id": "XP_047297173.1",
"transcript_support_level": null,
"aa_start": 1303,
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"cds_start": 3907,
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"cdna_start": 4045,
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"mane_select": null,
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"biotype": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 26,
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"exon_count": 38,
"intron_rank": null,
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"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_047441218.1",
"protein_id": "XP_047297174.1",
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_017028680.3",
"protein_id": "XP_016884169.1",
"transcript_support_level": null,
"aa_start": 1303,
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"cds_start": 3907,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
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"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_047441219.1",
"protein_id": "XP_047297175.1",
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"feature": null
},
{
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"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3772G>A",
"hgvs_p": "p.Glu1258Lys",
"transcript": "XM_005261419.3",
"protein_id": "XP_005261476.1",
"transcript_support_level": null,
"aa_start": 1258,
"aa_end": null,
"aa_length": 2210,
"cds_start": 3772,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3772G>A",
"hgvs_p": "p.Glu1258Lys",
"transcript": "XM_024452186.2",
"protein_id": "XP_024307954.1",
"transcript_support_level": null,
"aa_start": 1258,
"aa_end": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 24,
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"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3757G>A",
"hgvs_p": "p.Glu1253Lys",
"transcript": "XM_017028681.3",
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 24,
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"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3757G>A",
"hgvs_p": "p.Glu1253Lys",
"transcript": "XM_047441220.1",
"protein_id": "XP_047297176.1",
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},
{
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"strand": true,
"consequences": [
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],
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"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_006724180.3",
"protein_id": "XP_006724243.1",
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"aa_start": 1303,
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"aa_length": 2196,
"cds_start": 3907,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "K",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CABIN1",
"gene_hgnc_id": 24187,
"hgvs_c": "c.3907G>A",
"hgvs_p": "p.Glu1303Lys",
"transcript": "XM_047441221.1",
"protein_id": "XP_047297177.1",
"transcript_support_level": null,
"aa_start": 1303,
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"cds_start": 3907,
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"cdna_start": 4045,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "E",
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
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],
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{
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],
"clinvar_disease": "Prostate cancer",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Prostate cancer",
"pathogenicity_classification_combined": "Uncertain significance",
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}
],
"message": null
}