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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: 17-39665419-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=39665419&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 39665419,
"ref": "C",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000309889.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCAP",
"gene_hgnc_id": 11610,
"hgvs_c": "c.60C>G",
"hgvs_p": "p.Ala20Ala",
"transcript": "NM_003673.4",
"protein_id": "NP_003664.1",
"transcript_support_level": null,
"aa_start": 20,
"aa_end": null,
"aa_length": 167,
"cds_start": 60,
"cds_end": null,
"cds_length": 504,
"cdna_start": 71,
"cdna_end": null,
"cdna_length": 960,
"mane_select": "ENST00000309889.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCAP",
"gene_hgnc_id": 11610,
"hgvs_c": "c.60C>G",
"hgvs_p": "p.Ala20Ala",
"transcript": "ENST00000309889.3",
"protein_id": "ENSP00000312624.2",
"transcript_support_level": 1,
"aa_start": 20,
"aa_end": null,
"aa_length": 167,
"cds_start": 60,
"cds_end": null,
"cds_length": 504,
"cdna_start": 71,
"cdna_end": null,
"cdna_length": 960,
"mane_select": "NM_003673.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TCAP",
"gene_hgnc_id": 11610,
"hgvs_c": "c.60C>G",
"hgvs_p": "p.Ala20Ala",
"transcript": "ENST00000578283.1",
"protein_id": "ENSP00000462787.1",
"transcript_support_level": 5,
"aa_start": 20,
"aa_end": null,
"aa_length": 143,
"cds_start": 60,
"cds_end": null,
"cds_length": 432,
"cdna_start": 71,
"cdna_end": null,
"cdna_length": 583,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "TCAP",
"gene_hgnc_id": 11610,
"dbsnp": "rs146502276",
"frequency_reference_population": 0.0002528495,
"hom_count_reference_population": 0,
"allele_count_reference_population": 408,
"gnomad_exomes_af": 0.000247012,
"gnomad_genomes_af": 0.000308926,
"gnomad_exomes_ac": 361,
"gnomad_genomes_ac": 47,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.41999998688697815,
"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": -0.42,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.583,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate,BP6,BP7",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BP6",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000309889.3",
"gene_symbol": "TCAP",
"hgnc_id": 11610,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.60C>G",
"hgvs_p": "p.Ala20Ala"
}
],
"clinvar_disease": "Autosomal recessive limb-girdle muscular dystrophy type 2G,Cardiovascular phenotype,Hypertrophic cardiomyopathy 25,Primary familial hypertrophic cardiomyopathy,not provided,not specified",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:3 LB:6 B:2",
"phenotype_combined": "not specified|Hypertrophic cardiomyopathy 25|Cardiovascular phenotype|Autosomal recessive limb-girdle muscular dystrophy type 2G|not provided|Hypertrophic cardiomyopathy 25;Primary familial hypertrophic cardiomyopathy",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}