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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: 11-48144715-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=48144715&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 48144715,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "NM_002843.4",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"hgvs_c": "c.2616G>A",
"hgvs_p": "p.Glu872Glu",
"transcript": "NM_002843.4",
"protein_id": "NP_002834.3",
"transcript_support_level": null,
"aa_start": 872,
"aa_end": null,
"aa_length": 1337,
"cds_start": 2616,
"cds_end": null,
"cds_length": 4014,
"cdna_start": 2970,
"cdna_end": null,
"cdna_length": 7845,
"mane_select": "ENST00000418331.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"hgvs_c": "c.2616G>A",
"hgvs_p": "p.Glu872Glu",
"transcript": "ENST00000418331.7",
"protein_id": "ENSP00000400010.2",
"transcript_support_level": 1,
"aa_start": 872,
"aa_end": null,
"aa_length": 1337,
"cds_start": 2616,
"cds_end": null,
"cds_length": 4014,
"cdna_start": 2970,
"cdna_end": null,
"cdna_length": 7845,
"mane_select": "NM_002843.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"hgvs_c": "c.2958G>A",
"hgvs_p": "p.Glu986Glu",
"transcript": "ENST00000698881.1",
"protein_id": "ENSP00000514003.1",
"transcript_support_level": null,
"aa_start": 986,
"aa_end": null,
"aa_length": 1451,
"cds_start": 2958,
"cds_end": null,
"cds_length": 4356,
"cdna_start": 3104,
"cdna_end": null,
"cdna_length": 7979,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"hgvs_c": "c.2568G>A",
"hgvs_p": "p.Glu856Glu",
"transcript": "XM_017018085.2",
"protein_id": "XP_016873574.1",
"transcript_support_level": null,
"aa_start": 856,
"aa_end": null,
"aa_length": 1321,
"cds_start": 2568,
"cds_end": null,
"cds_length": 3966,
"cdna_start": 2580,
"cdna_end": null,
"cdna_length": 7455,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"hgvs_c": "c.2958G>A",
"hgvs_p": "p.Glu986Glu",
"transcript": "XM_047427374.1",
"protein_id": "XP_047283330.1",
"transcript_support_level": null,
"aa_start": 986,
"aa_end": null,
"aa_length": 1104,
"cds_start": 2958,
"cds_end": null,
"cds_length": 3315,
"cdna_start": 2970,
"cdna_end": null,
"cdna_length": 3404,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PTPRJ",
"gene_hgnc_id": 9673,
"dbsnp": "rs4752904",
"frequency_reference_population": 0.0000020523262,
"hom_count_reference_population": 0,
"allele_count_reference_population": 3,
"gnomad_exomes_af": 0.00000205233,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 3,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.9200000166893005,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.03999999910593033,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.92,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -3.981,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.04,
"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": "PM2,BP4_Strong,BP7",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 5,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "NM_002843.4",
"gene_symbol": "PTPRJ",
"hgnc_id": 9673,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD,Unknown,AR",
"hgvs_c": "c.2616G>A",
"hgvs_p": "p.Glu872Glu"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}