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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: 12-5996214-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=5996214&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 5996214,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000261405.10",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 52,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VWF",
"gene_hgnc_id": 12726,
"hgvs_c": "c.5851A>G",
"hgvs_p": "p.Thr1951Ala",
"transcript": "NM_000552.5",
"protein_id": "NP_000543.3",
"transcript_support_level": null,
"aa_start": 1951,
"aa_end": null,
"aa_length": 2813,
"cds_start": 5851,
"cds_end": null,
"cds_length": 8442,
"cdna_start": 6101,
"cdna_end": null,
"cdna_length": 8830,
"mane_select": "ENST00000261405.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 52,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VWF",
"gene_hgnc_id": 12726,
"hgvs_c": "c.5851A>G",
"hgvs_p": "p.Thr1951Ala",
"transcript": "ENST00000261405.10",
"protein_id": "ENSP00000261405.5",
"transcript_support_level": 1,
"aa_start": 1951,
"aa_end": null,
"aa_length": 2813,
"cds_start": 5851,
"cds_end": null,
"cds_length": 8442,
"cdna_start": 6101,
"cdna_end": null,
"cdna_length": 8830,
"mane_select": "NM_000552.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 52,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VWF",
"gene_hgnc_id": 12726,
"hgvs_c": "c.5851A>G",
"hgvs_p": "p.Thr1951Ala",
"transcript": "XM_047429501.1",
"protein_id": "XP_047285457.1",
"transcript_support_level": null,
"aa_start": 1951,
"aa_end": null,
"aa_length": 2813,
"cds_start": 5851,
"cds_end": null,
"cds_length": 8442,
"cdna_start": 6255,
"cdna_end": null,
"cdna_length": 8984,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "VWF",
"gene_hgnc_id": 12726,
"hgvs_c": "n.421-2280A>G",
"hgvs_p": null,
"transcript": "ENST00000538635.5",
"protein_id": null,
"transcript_support_level": 4,
"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": 475,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "VWF",
"gene_hgnc_id": 12726,
"dbsnp": "rs144072210",
"frequency_reference_population": 0.0004374247,
"hom_count_reference_population": 1,
"allele_count_reference_population": 705,
"gnomad_exomes_af": 0.000427536,
"gnomad_genomes_af": 0.000532264,
"gnomad_exomes_ac": 624,
"gnomad_genomes_ac": 81,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.042908281087875366,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.165,
"revel_prediction": "Benign",
"alphamissense_score": 0.0932,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.1,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.274,
"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": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PP2,BP4_Strong",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 4,
"pathogenic_score": 1,
"criteria": [
"PP2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000261405.10",
"gene_symbol": "VWF",
"hgnc_id": 12726,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.5851A>G",
"hgvs_p": "p.Thr1951Ala"
}
],
"clinvar_disease": "Abnormality of coagulation,Hereditary von Willebrand disease,not provided,not specified,von Willebrand disease type 1,von Willebrand disease type 2,von Willebrand disease type 3",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "LP:1 US:9",
"phenotype_combined": "not provided|Abnormality of coagulation|von Willebrand disease type 3|von Willebrand disease type 1|not specified|Hereditary von Willebrand disease|von Willebrand disease type 2|von Willebrand disease type 1;von Willebrand disease type 3",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}