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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: 6-89335377-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=89335377&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 89335377,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_016021.3",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe",
"transcript": "NM_016021.3",
"protein_id": "NP_057105.2",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 318,
"cds_start": 483,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000435041.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016021.3"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe",
"transcript": "ENST00000435041.3",
"protein_id": "ENSP00000451261.1",
"transcript_support_level": 1,
"aa_start": 161,
"aa_end": null,
"aa_length": 318,
"cds_start": 483,
"cds_end": null,
"cds_length": 957,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_016021.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000435041.3"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe",
"transcript": "ENST00000878541.1",
"protein_id": "ENSP00000548600.1",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 278,
"cds_start": 483,
"cds_end": null,
"cds_length": 837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878541.1"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.351G>T",
"hgvs_p": "p.Leu117Phe",
"transcript": "ENST00000941619.1",
"protein_id": "ENSP00000611678.1",
"transcript_support_level": null,
"aa_start": 117,
"aa_end": null,
"aa_length": 274,
"cds_start": 351,
"cds_end": null,
"cds_length": 825,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000941619.1"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe",
"transcript": "XM_011535887.3",
"protein_id": "XP_011534189.1",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 278,
"cds_start": 483,
"cds_end": null,
"cds_length": 837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535887.3"
},
{
"aa_ref": "L",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe",
"transcript": "XM_011535888.4",
"protein_id": "XP_011534190.1",
"transcript_support_level": null,
"aa_start": 161,
"aa_end": null,
"aa_length": 235,
"cds_start": 483,
"cds_end": null,
"cds_length": 708,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535888.4"
}
],
"gene_symbol": "UBE2J1",
"gene_hgnc_id": 17598,
"dbsnp": "rs748441409",
"frequency_reference_population": 0.000003109561,
"hom_count_reference_population": 0,
"allele_count_reference_population": 5,
"gnomad_exomes_af": 0.00000274755,
"gnomad_genomes_af": 0.00000657462,
"gnomad_exomes_ac": 4,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.28570958971977234,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.21,
"revel_prediction": "Benign",
"alphamissense_score": 0.1961,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.26,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.536,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_016021.3",
"gene_symbol": "UBE2J1",
"hgnc_id": 17598,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.483G>T",
"hgvs_p": "p.Leu161Phe"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}