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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: 11-119357489-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=119357489&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 119357489,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_004205.5",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp",
"transcript": "NM_004205.5",
"protein_id": "NP_004196.4",
"transcript_support_level": null,
"aa_start": 535,
"aa_end": null,
"aa_length": 605,
"cds_start": 1603,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1862,
"cdna_end": null,
"cdna_length": 3697,
"mane_select": "ENST00000260187.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp",
"transcript": "ENST00000260187.7",
"protein_id": "ENSP00000260187.2",
"transcript_support_level": 1,
"aa_start": 535,
"aa_end": null,
"aa_length": 605,
"cds_start": 1603,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1862,
"cdna_end": null,
"cdna_length": 3697,
"mane_select": "NM_004205.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.976A>G",
"hgvs_p": "p.Asn326Asp",
"transcript": "ENST00000525735.1",
"protein_id": "ENSP00000436952.1",
"transcript_support_level": 1,
"aa_start": 326,
"aa_end": null,
"aa_length": 396,
"cds_start": 976,
"cds_end": null,
"cds_length": 1191,
"cdna_start": 1188,
"cdna_end": null,
"cdna_length": 1704,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.874A>G",
"hgvs_p": "p.Asn292Asp",
"transcript": "ENST00000455332.6",
"protein_id": "ENSP00000407842.2",
"transcript_support_level": 1,
"aa_start": 292,
"aa_end": null,
"aa_length": 362,
"cds_start": 874,
"cds_end": null,
"cds_length": 1089,
"cdna_start": 1068,
"cdna_end": null,
"cdna_length": 2903,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.976A>G",
"hgvs_p": "p.Asn326Asp",
"transcript": "NM_171997.3",
"protein_id": "NP_741994.1",
"transcript_support_level": null,
"aa_start": 326,
"aa_end": null,
"aa_length": 396,
"cds_start": 976,
"cds_end": null,
"cds_length": 1191,
"cdna_start": 1189,
"cdna_end": null,
"cdna_length": 3024,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.874A>G",
"hgvs_p": "p.Asn292Asp",
"transcript": "NM_001243759.2",
"protein_id": "NP_001230688.1",
"transcript_support_level": null,
"aa_start": 292,
"aa_end": null,
"aa_length": 362,
"cds_start": 874,
"cds_end": null,
"cds_length": 1089,
"cdna_start": 1047,
"cdna_end": null,
"cdna_length": 2882,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp",
"transcript": "XM_005271721.6",
"protein_id": "XP_005271778.1",
"transcript_support_level": null,
"aa_start": 535,
"aa_end": null,
"aa_length": 605,
"cds_start": 1603,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 1705,
"cdna_end": null,
"cdna_length": 3540,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp",
"transcript": "XM_005271722.3",
"protein_id": "XP_005271779.1",
"transcript_support_level": null,
"aa_start": 535,
"aa_end": null,
"aa_length": 605,
"cds_start": 1603,
"cds_end": null,
"cds_length": 1818,
"cdna_start": 4488,
"cdna_end": null,
"cdna_length": 6323,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"hgvs_c": "c.844A>G",
"hgvs_p": "p.Asn282Asp",
"transcript": "XM_017018539.1",
"protein_id": "XP_016874028.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 352,
"cds_start": 844,
"cds_end": null,
"cds_length": 1059,
"cdna_start": 859,
"cdna_end": null,
"cdna_length": 2694,
"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": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "USP2-AS1",
"gene_hgnc_id": 48673,
"hgvs_c": "n.251+772T>C",
"hgvs_p": null,
"transcript": "ENST00000706409.1",
"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": 705,
"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": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "USP2-AS1",
"gene_hgnc_id": 48673,
"hgvs_c": "n.238+772T>C",
"hgvs_p": null,
"transcript": "ENST00000844114.1",
"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": 495,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "USP2",
"gene_hgnc_id": 12618,
"dbsnp": "rs1858413732",
"frequency_reference_population": 0.000004788394,
"hom_count_reference_population": 0,
"allele_count_reference_population": 7,
"gnomad_exomes_af": 0.00000478839,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 7,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09497153759002686,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.019999999552965164,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.054,
"revel_prediction": "Benign",
"alphamissense_score": 0.1335,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.7,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.026,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.02,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_004205.5",
"gene_symbol": "USP2",
"hgnc_id": 12618,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1603A>G",
"hgvs_p": "p.Asn535Asp"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000706409.1",
"gene_symbol": "USP2-AS1",
"hgnc_id": 48673,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.251+772T>C",
"hgvs_p": null
}
],
"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
}