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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: 17-81402198-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=81402198&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 81402198,
"ref": "C",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000675386.2",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "NM_001377448.1",
"protein_id": "NP_001364377.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2608,
"cds_start": -4,
"cds_end": null,
"cds_length": 7827,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10726,
"mane_select": "ENST00000675386.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "ENST00000675386.2",
"protein_id": "ENSP00000502710.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2608,
"cds_start": -4,
"cds_end": null,
"cds_length": 7827,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10726,
"mane_select": "NM_001377448.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 1,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "n.1109C>T",
"hgvs_p": null,
"transcript": "ENST00000625166.1",
"protein_id": null,
"transcript_support_level": 6,
"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": 1890,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "NM_001291324.3",
"protein_id": "NP_001278253.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2639,
"cds_start": -4,
"cds_end": null,
"cds_length": 7920,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10819,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "ENST00000584436.7",
"protein_id": "ENSP00000462154.4",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 2639,
"cds_start": -4,
"cds_end": null,
"cds_length": 7920,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10801,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "XM_047436466.1",
"protein_id": "XP_047292422.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2639,
"cds_start": -4,
"cds_end": null,
"cds_length": 7920,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10765,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "XM_011525063.3",
"protein_id": "XP_011523365.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2631,
"cds_start": -4,
"cds_end": null,
"cds_length": 7896,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null,
"transcript": "XM_047436467.1",
"protein_id": "XP_047292423.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2631,
"cds_start": -4,
"cds_end": null,
"cds_length": 7896,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "BAHCC1",
"gene_hgnc_id": 29279,
"dbsnp": "rs1701",
"frequency_reference_population": 0.000065764376,
"hom_count_reference_population": 0,
"allele_count_reference_population": 10,
"gnomad_exomes_af": 0,
"gnomad_genomes_af": 0.0000657644,
"gnomad_exomes_ac": 0,
"gnomad_genomes_ac": 10,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.800000011920929,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"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": -0.8,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.017,
"phylop100way_prediction": "Benign",
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000675386.2",
"gene_symbol": "BAHCC1",
"hgnc_id": 29279,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.178+2281C>T",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}