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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: 3-167807276-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=167807276&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 167807276,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001122752.2",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val",
"transcript": "NM_001122752.2",
"protein_id": "NP_001116224.1",
"transcript_support_level": null,
"aa_start": 305,
"aa_end": null,
"aa_length": 410,
"cds_start": 914,
"cds_end": null,
"cds_length": 1233,
"cdna_start": 1035,
"cdna_end": null,
"cdna_length": 1600,
"mane_select": "ENST00000446050.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val",
"transcript": "ENST00000446050.7",
"protein_id": "ENSP00000397373.2",
"transcript_support_level": 1,
"aa_start": 305,
"aa_end": null,
"aa_length": 410,
"cds_start": 914,
"cds_end": null,
"cds_length": 1233,
"cdna_start": 1035,
"cdna_end": null,
"cdna_length": 1600,
"mane_select": "NM_001122752.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val",
"transcript": "ENST00000295777.9",
"protein_id": "ENSP00000295777.5",
"transcript_support_level": 1,
"aa_start": 305,
"aa_end": null,
"aa_length": 410,
"cds_start": 914,
"cds_end": null,
"cds_length": 1233,
"cdna_start": 1345,
"cdna_end": null,
"cdna_length": 1907,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val",
"transcript": "NM_005025.5",
"protein_id": "NP_005016.1",
"transcript_support_level": null,
"aa_start": 305,
"aa_end": null,
"aa_length": 410,
"cds_start": 914,
"cds_end": null,
"cds_length": 1233,
"cdna_start": 1347,
"cdna_end": null,
"cdna_length": 1912,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.38A>T",
"hgvs_p": "p.Asp13Val",
"transcript": "ENST00000466865.1",
"protein_id": "ENSP00000420807.1",
"transcript_support_level": 2,
"aa_start": 13,
"aa_end": null,
"aa_length": 118,
"cds_start": 38,
"cds_end": null,
"cds_length": 357,
"cdna_start": 39,
"cdna_end": null,
"cdna_length": 595,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val",
"transcript": "XM_017006618.3",
"protein_id": "XP_016862107.1",
"transcript_support_level": null,
"aa_start": 305,
"aa_end": null,
"aa_length": 410,
"cds_start": 914,
"cds_end": null,
"cds_length": 1233,
"cdna_start": 1024,
"cdna_end": null,
"cdna_length": 1589,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"hgvs_c": "n.110A>T",
"hgvs_p": null,
"transcript": "ENST00000488374.5",
"protein_id": null,
"transcript_support_level": 3,
"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": 668,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000287319",
"gene_hgnc_id": null,
"hgvs_c": "n.545+3261T>A",
"hgvs_p": null,
"transcript": "ENST00000661269.1",
"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": 1359,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SERPINI1",
"gene_hgnc_id": 8943,
"dbsnp": "rs756818970",
"frequency_reference_population": 0.000016741673,
"hom_count_reference_population": 0,
"allele_count_reference_population": 27,
"gnomad_exomes_af": 0.0000178013,
"gnomad_genomes_af": 0.00000657142,
"gnomad_exomes_ac": 26,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.3586505651473999,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.404,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.1388,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.14,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.17,
"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": "BP4,BS2",
"acmg_by_gene": [
{
"score": -5,
"benign_score": 5,
"pathogenic_score": 0,
"criteria": [
"BP4",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_001122752.2",
"gene_symbol": "SERPINI1",
"hgnc_id": 8943,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.914A>T",
"hgvs_p": "p.Asp305Val"
},
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000661269.1",
"gene_symbol": "ENSG00000287319",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.545+3261T>A",
"hgvs_p": null
}
],
"clinvar_disease": "Familial encephalopathy with neuroserpin inclusion bodies",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Familial encephalopathy with neuroserpin inclusion bodies",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}