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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: X-139561992-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=139561992&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 139561992,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000218099.7",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "c.1307C>T",
"hgvs_p": "p.Ala436Val",
"transcript": "NM_000133.4",
"protein_id": "NP_000124.1",
"transcript_support_level": null,
"aa_start": 436,
"aa_end": null,
"aa_length": 461,
"cds_start": 1307,
"cds_end": null,
"cds_length": 1386,
"cdna_start": 1333,
"cdna_end": null,
"cdna_length": 2800,
"mane_select": "ENST00000218099.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "c.1307C>T",
"hgvs_p": "p.Ala436Val",
"transcript": "ENST00000218099.7",
"protein_id": "ENSP00000218099.2",
"transcript_support_level": 1,
"aa_start": 436,
"aa_end": null,
"aa_length": 461,
"cds_start": 1307,
"cds_end": null,
"cds_length": 1386,
"cdna_start": 1333,
"cdna_end": null,
"cdna_length": 2800,
"mane_select": "NM_000133.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "c.1193C>T",
"hgvs_p": "p.Ala398Val",
"transcript": "ENST00000394090.2",
"protein_id": "ENSP00000377650.2",
"transcript_support_level": 1,
"aa_start": 398,
"aa_end": null,
"aa_length": 423,
"cds_start": 1193,
"cds_end": null,
"cds_length": 1272,
"cdna_start": 1193,
"cdna_end": null,
"cdna_length": 1272,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "c.1193C>T",
"hgvs_p": "p.Ala398Val",
"transcript": "NM_001313913.2",
"protein_id": "NP_001300842.1",
"transcript_support_level": null,
"aa_start": 398,
"aa_end": null,
"aa_length": 423,
"cds_start": 1193,
"cds_end": null,
"cds_length": 1272,
"cdna_start": 1219,
"cdna_end": null,
"cdna_length": 2686,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "c.1178C>T",
"hgvs_p": "p.Ala393Val",
"transcript": "XM_005262397.5",
"protein_id": "XP_005262454.1",
"transcript_support_level": null,
"aa_start": 393,
"aa_end": null,
"aa_length": 418,
"cds_start": 1178,
"cds_end": null,
"cds_length": 1257,
"cdna_start": 1204,
"cdna_end": null,
"cdna_length": 2671,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"hgvs_c": "n.1723+251C>T",
"hgvs_p": null,
"transcript": "ENST00000643157.1",
"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": 1919,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "F9",
"gene_hgnc_id": 3551,
"dbsnp": "rs137852266",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.992354691028595,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.936,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.8916,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.68,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.879,
"phylop100way_prediction": "Pathogenic",
"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": "PM1,PM2,PM5,PP2,PP3_Strong,PP5",
"acmg_by_gene": [
{
"score": 12,
"benign_score": 0,
"pathogenic_score": 12,
"criteria": [
"PM1",
"PM2",
"PM5",
"PP2",
"PP3_Strong",
"PP5"
],
"verdict": "Pathogenic",
"transcript": "ENST00000218099.7",
"gene_symbol": "F9",
"hgnc_id": 3551,
"effects": [
"missense_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "c.1307C>T",
"hgvs_p": "p.Ala436Val"
}
],
"clinvar_disease": "Hereditary factor IX deficiency disease",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Hereditary factor IX deficiency disease",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}