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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: 14-23400875-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=23400875&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 23400875,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000405093.9",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH6",
"gene_hgnc_id": 7576,
"hgvs_c": "c.1244G>C",
"hgvs_p": "p.Gly415Ala",
"transcript": "NM_002471.4",
"protein_id": "NP_002462.2",
"transcript_support_level": null,
"aa_start": 415,
"aa_end": null,
"aa_length": 1939,
"cds_start": 1244,
"cds_end": null,
"cds_length": 5820,
"cdna_start": 1311,
"cdna_end": null,
"cdna_length": 5940,
"mane_select": "ENST00000405093.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH6",
"gene_hgnc_id": 7576,
"hgvs_c": "c.1244G>C",
"hgvs_p": "p.Gly415Ala",
"transcript": "ENST00000405093.9",
"protein_id": "ENSP00000386041.3",
"transcript_support_level": 5,
"aa_start": 415,
"aa_end": null,
"aa_length": 1939,
"cds_start": 1244,
"cds_end": null,
"cds_length": 5820,
"cdna_start": 1311,
"cdna_end": null,
"cdna_length": 5940,
"mane_select": "NM_002471.4",
"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": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYH6",
"gene_hgnc_id": 7576,
"hgvs_c": "n.1311G>C",
"hgvs_p": null,
"transcript": "ENST00000557461.2",
"protein_id": null,
"transcript_support_level": 5,
"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": 2192,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "MYH6",
"gene_hgnc_id": 7576,
"dbsnp": "rs759520932",
"frequency_reference_population": 0.000042128584,
"hom_count_reference_population": 0,
"allele_count_reference_population": 68,
"gnomad_exomes_af": 0.0000396746,
"gnomad_genomes_af": 0.0000656978,
"gnomad_exomes_ac": 58,
"gnomad_genomes_ac": 10,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5344603657722473,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.803,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.922,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.05,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 5.753,
"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": -5,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP6,BS2",
"acmg_by_gene": [
{
"score": -5,
"benign_score": 5,
"pathogenic_score": 0,
"criteria": [
"BP6",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000405093.9",
"gene_symbol": "MYH6",
"hgnc_id": 7576,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1244G>C",
"hgvs_p": "p.Gly415Ala"
}
],
"clinvar_disease": " susceptibility to,Atrial septal defect 3,Cardiovascular phenotype,Dilated cardiomyopathy 1EE,Hypertrophic cardiomyopathy 1,Hypertrophic cardiomyopathy 14,Sick sinus syndrome 3,not provided",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:3 LB:2",
"phenotype_combined": "Hypertrophic cardiomyopathy 14|Hypertrophic cardiomyopathy 14;Dilated cardiomyopathy 1EE;Hypertrophic cardiomyopathy 1;Sick sinus syndrome 3, susceptibility to;Atrial septal defect 3|Cardiovascular phenotype|Hypertrophic cardiomyopathy 14;Dilated cardiomyopathy 1EE;Sick sinus syndrome 3, susceptibility to|not provided",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}