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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: 12-32824141-AG-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=32824141&ref=AG&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 32824141,
"ref": "AG",
"alt": "A",
"effect": "frameshift_variant",
"transcript": "ENST00000340811.9",
"consequences": [
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "NM_001005242.3",
"protein_id": "NP_001005242.2",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 837,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2514,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 4229,
"mane_select": "ENST00000340811.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "ENST00000340811.9",
"protein_id": "ENSP00000342800.5",
"transcript_support_level": 1,
"aa_start": 526,
"aa_end": null,
"aa_length": 837,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2514,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 4229,
"mane_select": "NM_001005242.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1709delC",
"hgvs_p": "p.Ala570fs",
"transcript": "ENST00000070846.11",
"protein_id": "ENSP00000070846.6",
"transcript_support_level": 1,
"aa_start": 570,
"aa_end": null,
"aa_length": 881,
"cds_start": 1709,
"cds_end": null,
"cds_length": 2646,
"cdna_start": 1755,
"cdna_end": null,
"cdna_length": 4361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1709delC",
"hgvs_p": "p.Ala570fs",
"transcript": "NM_004572.4",
"protein_id": "NP_004563.2",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 881,
"cds_start": 1709,
"cds_end": null,
"cds_length": 2646,
"cdna_start": 1755,
"cdna_end": null,
"cdna_length": 4361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "NM_001407155.1",
"protein_id": "NP_001394084.1",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 822,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2469,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 4039,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "ENST00000700559.2",
"protein_id": "ENSP00000515065.2",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 822,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2469,
"cdna_start": 1644,
"cdna_end": null,
"cdna_length": 4070,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "NM_001407156.1",
"protein_id": "NP_001394085.1",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 782,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2349,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 4064,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1709delC",
"hgvs_p": "p.Ala570fs",
"transcript": "NM_001407157.1",
"protein_id": "NP_001394086.1",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 730,
"cds_start": 1709,
"cds_end": null,
"cds_length": 2193,
"cdna_start": 1755,
"cdna_end": null,
"cdna_length": 3403,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1250delC",
"hgvs_p": "p.Ala417fs",
"transcript": "NM_001407158.1",
"protein_id": "NP_001394087.1",
"transcript_support_level": null,
"aa_start": 417,
"aa_end": null,
"aa_length": 728,
"cds_start": 1250,
"cds_end": null,
"cds_length": 2187,
"cdna_start": 2122,
"cdna_end": null,
"cdna_length": 4728,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1250delC",
"hgvs_p": "p.Ala417fs",
"transcript": "NM_001407159.1",
"protein_id": "NP_001394088.1",
"transcript_support_level": null,
"aa_start": 417,
"aa_end": null,
"aa_length": 728,
"cds_start": 1250,
"cds_end": null,
"cds_length": 2187,
"cdna_start": 1886,
"cdna_end": null,
"cdna_length": 4492,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1250delC",
"hgvs_p": "p.Ala417fs",
"transcript": "NM_001407160.1",
"protein_id": "NP_001394089.1",
"transcript_support_level": null,
"aa_start": 417,
"aa_end": null,
"aa_length": 713,
"cds_start": 1250,
"cds_end": null,
"cds_length": 2142,
"cdna_start": 1886,
"cdna_end": null,
"cdna_length": 4302,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "NM_001407161.1",
"protein_id": "NP_001394090.1",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 686,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2061,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 3271,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "ENST00000700564.2",
"protein_id": "ENSP00000519095.1",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 686,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2061,
"cdna_start": 1581,
"cdna_end": null,
"cdna_length": 3156,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs",
"transcript": "ENST00000700563.2",
"protein_id": "ENSP00000515066.2",
"transcript_support_level": null,
"aa_start": 526,
"aa_end": null,
"aa_length": 682,
"cds_start": 1577,
"cds_end": null,
"cds_length": 2049,
"cdna_start": 1623,
"cdna_end": null,
"cdna_length": 3015,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "c.1250delC",
"hgvs_p": "p.Ala417fs",
"transcript": "NM_001407162.1",
"protein_id": "NP_001394091.1",
"transcript_support_level": null,
"aa_start": 417,
"aa_end": null,
"aa_length": 577,
"cds_start": 1250,
"cds_end": null,
"cds_length": 1734,
"cdna_start": 2122,
"cdna_end": null,
"cdna_length": 3770,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "n.264delC",
"hgvs_p": null,
"transcript": "ENST00000546498.2",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1519,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "n.89delC",
"hgvs_p": null,
"transcript": "ENST00000700555.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2696,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "n.792delC",
"hgvs_p": null,
"transcript": "ENST00000700560.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2433,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"hgvs_c": "n.918delC",
"hgvs_p": null,
"transcript": "ENST00000700561.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2226,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PKP2",
"gene_hgnc_id": 9024,
"dbsnp": "rs397517005",
"frequency_reference_population": 0.0000013697542,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000136975,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": null,
"computational_prediction_selected": null,
"computational_source_selected": null,
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 5.506,
"phylop100way_prediction": "Uncertain_significance",
"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": 12,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PVS1,PM2,PP5_Moderate",
"acmg_by_gene": [
{
"score": 12,
"benign_score": 0,
"pathogenic_score": 12,
"criteria": [
"PVS1",
"PM2",
"PP5_Moderate"
],
"verdict": "Pathogenic",
"transcript": "ENST00000340811.9",
"gene_symbol": "PKP2",
"hgnc_id": 9024,
"effects": [
"frameshift_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1577delC",
"hgvs_p": "p.Ala526fs"
}
],
"clinvar_disease": "Arrhythmogenic right ventricular cardiomyopathy",
"clinvar_classification": "Likely pathogenic",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LP:1",
"phenotype_combined": "Arrhythmogenic right ventricular cardiomyopathy",
"pathogenicity_classification_combined": "Likely pathogenic",
"custom_annotations": null
}
],
"message": null
}