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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: 4-39232271-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=39232271&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 39232271,
"ref": "A",
"alt": "T",
"effect": "missense_variant,splice_region_variant",
"transcript": "ENST00000399820.8",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "NM_025132.4",
"protein_id": "NP_079408.3",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 1342,
"cds_start": 2252,
"cds_end": null,
"cds_length": 4029,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 4395,
"mane_select": "ENST00000399820.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "ENST00000399820.8",
"protein_id": "ENSP00000382717.3",
"transcript_support_level": 1,
"aa_start": 751,
"aa_end": null,
"aa_length": 1342,
"cds_start": 2252,
"cds_end": null,
"cds_length": 4029,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 4395,
"mane_select": "NM_025132.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 37,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "XM_011513724.2",
"protein_id": "XP_011512026.1",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 1346,
"cds_start": 2252,
"cds_end": null,
"cds_length": 4041,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 4407,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2186A>T",
"hgvs_p": "p.Glu729Val",
"transcript": "XM_011513725.3",
"protein_id": "XP_011512027.1",
"transcript_support_level": null,
"aa_start": 729,
"aa_end": null,
"aa_length": 1324,
"cds_start": 2186,
"cds_end": null,
"cds_length": 3975,
"cdna_start": 2215,
"cdna_end": null,
"cdna_length": 4341,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "XM_047416031.1",
"protein_id": "XP_047271987.1",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 1195,
"cds_start": 2252,
"cds_end": null,
"cds_length": 3588,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 5387,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.1772A>T",
"hgvs_p": "p.Glu591Val",
"transcript": "XM_047416033.1",
"protein_id": "XP_047271989.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1772,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 1935,
"cdna_end": null,
"cdna_length": 4061,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "XM_047416034.1",
"protein_id": "XP_047271990.1",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 969,
"cds_start": 2252,
"cds_end": null,
"cds_length": 2910,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 2978,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "XM_047416035.1",
"protein_id": "XP_047271991.1",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 761,
"cds_start": 2252,
"cds_end": null,
"cds_length": 2286,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 2377,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.1772A>T",
"hgvs_p": "p.Glu591Val",
"transcript": "NM_001317924.2",
"protein_id": "NP_001304853.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 1182,
"cds_start": 1772,
"cds_end": null,
"cds_length": 3549,
"cdna_start": 2165,
"cdna_end": null,
"cdna_length": 4279,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2186A>T",
"hgvs_p": "p.Glu729Val",
"transcript": "XM_047416030.1",
"protein_id": "XP_047271986.1",
"transcript_support_level": null,
"aa_start": 729,
"aa_end": null,
"aa_length": 1320,
"cds_start": 2186,
"cds_end": null,
"cds_length": 3963,
"cdna_start": 2215,
"cdna_end": null,
"cdna_length": 4329,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant",
"splice_region_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val",
"transcript": "XM_047416032.1",
"protein_id": "XP_047271988.1",
"transcript_support_level": null,
"aa_start": 751,
"aa_end": null,
"aa_length": 1191,
"cds_start": 2252,
"cds_end": null,
"cds_length": 3576,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 5375,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.*1833A>T",
"hgvs_p": null,
"transcript": "ENST00000506869.5",
"protein_id": "ENSP00000424319.1",
"transcript_support_level": 2,
"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": 4249,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.400A>T",
"hgvs_p": null,
"transcript": "ENST00000507228.1",
"protein_id": "ENSP00000421401.1",
"transcript_support_level": 4,
"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": 571,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.443A>T",
"hgvs_p": null,
"transcript": "ENST00000511729.5",
"protein_id": null,
"transcript_support_level": 5,
"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": 510,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.1250A>T",
"hgvs_p": null,
"transcript": "ENST00000512095.5",
"protein_id": null,
"transcript_support_level": 2,
"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": 3095,
"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": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.406A>T",
"hgvs_p": null,
"transcript": "ENST00000515631.1",
"protein_id": null,
"transcript_support_level": 4,
"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": 553,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"hgvs_c": "n.*1833A>T",
"hgvs_p": null,
"transcript": "ENST00000506869.5",
"protein_id": "ENSP00000424319.1",
"transcript_support_level": 2,
"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": 4249,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "WDR19",
"gene_hgnc_id": 18340,
"dbsnp": "rs778651224",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8840804696083069,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.9940000176429749,
"splice_prediction_selected": "Pathogenic",
"splice_source_selected": "dbscSNV1_RF",
"revel_score": 0.856,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.3755,
"alphamissense_prediction": "Uncertain_significance",
"bayesdelnoaf_score": 0.36,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 9.023,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.83,
"spliceai_max_prediction": "Pathogenic",
"dbscsnv_ada_score": 0.999899933376707,
"dbscsnv_ada_prediction": "Pathogenic",
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 4,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3_Moderate",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000399820.8",
"gene_symbol": "WDR19",
"hgnc_id": 18340,
"effects": [
"missense_variant",
"splice_region_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2252A>T",
"hgvs_p": "p.Glu751Val"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}