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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: 9-15469976-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=15469976&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 15469976,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_033222.5",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "NM_033222.5",
"protein_id": "NP_150091.2",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000380733.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_033222.5"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000380733.9",
"protein_id": "ENSP00000370109.4",
"transcript_support_level": 1,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_033222.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380733.9"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000380738.8",
"protein_id": "ENSP00000370114.4",
"transcript_support_level": 1,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380738.8"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000950213.1",
"protein_id": "ENSP00000620272.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 542,
"cds_start": 995,
"cds_end": null,
"cds_length": 1629,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950213.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "NM_001128217.3",
"protein_id": "NP_001121689.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001128217.3"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000901729.1",
"protein_id": "ENSP00000571788.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901729.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000901731.1",
"protein_id": "ENSP00000571790.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901731.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000901732.1",
"protein_id": "ENSP00000571791.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901732.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000901733.1",
"protein_id": "ENSP00000571792.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901733.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000917556.1",
"protein_id": "ENSP00000587615.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917556.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000917558.1",
"protein_id": "ENSP00000587617.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917558.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000917559.1",
"protein_id": "ENSP00000587618.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917559.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000917561.1",
"protein_id": "ENSP00000587620.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917561.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000950211.1",
"protein_id": "ENSP00000620270.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950211.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000950214.1",
"protein_id": "ENSP00000620273.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 530,
"cds_start": 995,
"cds_end": null,
"cds_length": 1593,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950214.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.992G>A",
"hgvs_p": "p.Gly331Glu",
"transcript": "ENST00000917560.1",
"protein_id": "ENSP00000587619.1",
"transcript_support_level": null,
"aa_start": 331,
"aa_end": null,
"aa_length": 529,
"cds_start": 992,
"cds_end": null,
"cds_length": 1590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917560.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.992G>A",
"hgvs_p": "p.Gly331Glu",
"transcript": "ENST00000950212.1",
"protein_id": "ENSP00000620271.1",
"transcript_support_level": null,
"aa_start": 331,
"aa_end": null,
"aa_length": 529,
"cds_start": 992,
"cds_end": null,
"cds_length": 1590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950212.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000901730.1",
"protein_id": "ENSP00000571789.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 514,
"cds_start": 995,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901730.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu",
"transcript": "ENST00000917557.1",
"protein_id": "ENSP00000587616.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 514,
"cds_start": 995,
"cds_end": null,
"cds_length": 1545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917557.1"
},
{
"aa_ref": "G",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"hgvs_c": "c.515G>A",
"hgvs_p": "p.Gly172Glu",
"transcript": "ENST00000950215.1",
"protein_id": "ENSP00000620274.1",
"transcript_support_level": null,
"aa_start": 172,
"aa_end": null,
"aa_length": 370,
"cds_start": 515,
"cds_end": null,
"cds_length": 1113,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950215.1"
}
],
"gene_symbol": "PSIP1",
"gene_hgnc_id": 9527,
"dbsnp": "rs200620037",
"frequency_reference_population": 0.0000068710387,
"hom_count_reference_population": 0,
"allele_count_reference_population": 10,
"gnomad_exomes_af": 0.00000687104,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 10,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09216108918190002,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.03999999910593033,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.136,
"revel_prediction": "Benign",
"alphamissense_score": 0.3073,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.46,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.54,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate,BS2",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_033222.5",
"gene_symbol": "PSIP1",
"hgnc_id": 9527,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.995G>A",
"hgvs_p": "p.Gly332Glu"
}
],
"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
}