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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: X-124381101-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=124381101&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 124381101,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001163278.2",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7634A>T",
"hgvs_p": "p.Asp2545Val",
"transcript": "NM_001163278.2",
"protein_id": "NP_001156750.1",
"transcript_support_level": null,
"aa_start": 2545,
"aa_end": null,
"aa_length": 2732,
"cds_start": 7634,
"cds_end": null,
"cds_length": 8199,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000422452.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001163278.2"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7634A>T",
"hgvs_p": "p.Asp2545Val",
"transcript": "ENST00000422452.4",
"protein_id": "ENSP00000403954.4",
"transcript_support_level": 1,
"aa_start": 2545,
"aa_end": null,
"aa_length": 2732,
"cds_start": 7634,
"cds_end": null,
"cds_length": 8199,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001163278.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000422452.4"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7613A>T",
"hgvs_p": "p.Asp2538Val",
"transcript": "ENST00000371130.7",
"protein_id": "ENSP00000360171.3",
"transcript_support_level": 1,
"aa_start": 2538,
"aa_end": null,
"aa_length": 2725,
"cds_start": 7613,
"cds_end": null,
"cds_length": 8178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000371130.7"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7631A>T",
"hgvs_p": "p.Asp2544Val",
"transcript": "NM_001163279.1",
"protein_id": "NP_001156751.1",
"transcript_support_level": null,
"aa_start": 2544,
"aa_end": null,
"aa_length": 2731,
"cds_start": 7631,
"cds_end": null,
"cds_length": 8196,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001163279.1"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7613A>T",
"hgvs_p": "p.Asp2538Val",
"transcript": "NM_014253.3",
"protein_id": "NP_055068.2",
"transcript_support_level": null,
"aa_start": 2538,
"aa_end": null,
"aa_length": 2725,
"cds_start": 7613,
"cds_end": null,
"cds_length": 8178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014253.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_017029208.3",
"protein_id": "XP_016884697.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029208.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_017029209.3",
"protein_id": "XP_016884698.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029209.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_017029210.3",
"protein_id": "XP_016884699.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029210.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 36,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_017029211.3",
"protein_id": "XP_016884700.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029211.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_017029213.3",
"protein_id": "XP_016884702.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029213.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 37,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7733A>T",
"hgvs_p": "p.Asp2578Val",
"transcript": "XM_047441759.1",
"protein_id": "XP_047297715.1",
"transcript_support_level": null,
"aa_start": 2578,
"aa_end": null,
"aa_length": 2765,
"cds_start": 7733,
"cds_end": null,
"cds_length": 8298,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047441759.1"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7613A>T",
"hgvs_p": "p.Asp2538Val",
"transcript": "XM_017029214.3",
"protein_id": "XP_016884703.1",
"transcript_support_level": null,
"aa_start": 2538,
"aa_end": null,
"aa_length": 2725,
"cds_start": 7613,
"cds_end": null,
"cds_length": 8178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017029214.3"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.7589A>T",
"hgvs_p": "p.Asp2530Val",
"transcript": "XM_047441760.1",
"protein_id": "XP_047297716.1",
"transcript_support_level": null,
"aa_start": 2530,
"aa_end": null,
"aa_length": 2717,
"cds_start": 7589,
"cds_end": null,
"cds_length": 8154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047441760.1"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.5339A>T",
"hgvs_p": "p.Asp1780Val",
"transcript": "XM_011531236.4",
"protein_id": "XP_011529538.2",
"transcript_support_level": null,
"aa_start": 1780,
"aa_end": null,
"aa_length": 1967,
"cds_start": 5339,
"cds_end": null,
"cds_length": 5904,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531236.4"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.3986A>T",
"hgvs_p": "p.Asp1329Val",
"transcript": "XM_047441761.1",
"protein_id": "XP_047297717.1",
"transcript_support_level": null,
"aa_start": 1329,
"aa_end": null,
"aa_length": 1516,
"cds_start": 3986,
"cds_end": null,
"cds_length": 4551,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047441761.1"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.3887A>T",
"hgvs_p": "p.Asp1296Val",
"transcript": "XM_047441762.1",
"protein_id": "XP_047297718.1",
"transcript_support_level": null,
"aa_start": 1296,
"aa_end": null,
"aa_length": 1483,
"cds_start": 3887,
"cds_end": null,
"cds_length": 4452,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047441762.1"
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"hgvs_c": "c.3638A>T",
"hgvs_p": "p.Asp1213Val",
"transcript": "XM_011531237.3",
"protein_id": "XP_011529539.1",
"transcript_support_level": null,
"aa_start": 1213,
"aa_end": null,
"aa_length": 1400,
"cds_start": 3638,
"cds_end": null,
"cds_length": 4203,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531237.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "STAG2",
"gene_hgnc_id": 11355,
"hgvs_c": "n.454-30721T>A",
"hgvs_p": null,
"transcript": "ENST00000469481.1",
"protein_id": null,
"transcript_support_level": 3,
"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": "pseudogene",
"feature": "ENST00000469481.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "LOC105373331",
"gene_hgnc_id": null,
"hgvs_c": "n.88+107T>A",
"hgvs_p": null,
"transcript": "XR_938576.1",
"protein_id": null,
"transcript_support_level": null,
"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": "pseudogene",
"feature": "XR_938576.1"
}
],
"gene_symbol": "TENM1",
"gene_hgnc_id": 8117,
"dbsnp": "rs1295657021",
"frequency_reference_population": 0.000007288311,
"hom_count_reference_population": 3,
"allele_count_reference_population": 8,
"gnomad_exomes_af": 0.00000728831,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 8,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8329019546508789,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.722,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.3307,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.14,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 8.017,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0,
"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": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PP3,BS2",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 4,
"pathogenic_score": 1,
"criteria": [
"PP3",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_001163278.2",
"gene_symbol": "TENM1",
"hgnc_id": 8117,
"effects": [
"missense_variant"
],
"inheritance_mode": "XL,AD",
"hgvs_c": "c.7634A>T",
"hgvs_p": "p.Asp2545Val"
},
{
"score": -3,
"benign_score": 4,
"pathogenic_score": 1,
"criteria": [
"PP3",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000469481.1",
"gene_symbol": "STAG2",
"hgnc_id": 11355,
"effects": [
"intron_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "n.454-30721T>A",
"hgvs_p": null
},
{
"score": -3,
"benign_score": 4,
"pathogenic_score": 1,
"criteria": [
"PP3",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "XR_938576.1",
"gene_symbol": "LOC105373331",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.88+107T>A",
"hgvs_p": null
}
],
"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
}