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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: 22-20813451-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=20813451&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 20813451,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000255882.11",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.912C>G",
"hgvs_p": "p.Ile304Met",
"transcript": "NM_058004.4",
"protein_id": "NP_477352.3",
"transcript_support_level": null,
"aa_start": 304,
"aa_end": null,
"aa_length": 2102,
"cds_start": 912,
"cds_end": null,
"cds_length": 6309,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 6751,
"mane_select": "ENST00000255882.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.912C>G",
"hgvs_p": "p.Ile304Met",
"transcript": "ENST00000255882.11",
"protein_id": "ENSP00000255882.6",
"transcript_support_level": 1,
"aa_start": 304,
"aa_end": null,
"aa_length": 2102,
"cds_start": 912,
"cds_end": null,
"cds_length": 6309,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 6751,
"mane_select": "NM_058004.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.912C>G",
"hgvs_p": "p.Ile304Met",
"transcript": "NM_001362863.2",
"protein_id": "NP_001349792.1",
"transcript_support_level": null,
"aa_start": 304,
"aa_end": null,
"aa_length": 2080,
"cds_start": 912,
"cds_end": null,
"cds_length": 6243,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 6685,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.912C>G",
"hgvs_p": "p.Ile304Met",
"transcript": "NM_001362862.2",
"protein_id": "NP_001349791.1",
"transcript_support_level": null,
"aa_start": 304,
"aa_end": null,
"aa_length": 2071,
"cds_start": 912,
"cds_end": null,
"cds_length": 6216,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 6658,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 51,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.996C>G",
"hgvs_p": "p.Ile332Met",
"transcript": "XM_047441408.1",
"protein_id": "XP_047297364.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 1983,
"cds_start": 996,
"cds_end": null,
"cds_length": 5952,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 5980,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 48,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.996C>G",
"hgvs_p": "p.Ile332Met",
"transcript": "XM_005261635.2",
"protein_id": "XP_005261692.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 1854,
"cds_start": 996,
"cds_end": null,
"cds_length": 5565,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 5923,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.996C>G",
"hgvs_p": "p.Ile332Met",
"transcript": "XM_011530226.2",
"protein_id": "XP_011528528.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 1416,
"cds_start": 996,
"cds_end": null,
"cds_length": 4251,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 4268,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.996C>G",
"hgvs_p": "p.Ile332Met",
"transcript": "XM_047441409.1",
"protein_id": "XP_047297365.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 1286,
"cds_start": 996,
"cds_end": null,
"cds_length": 3861,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 4010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "c.996C>G",
"hgvs_p": "p.Ile332Met",
"transcript": "XM_011530228.3",
"protein_id": "XP_011528530.1",
"transcript_support_level": null,
"aa_start": 332,
"aa_end": null,
"aa_length": 1277,
"cds_start": 996,
"cds_end": null,
"cds_length": 3834,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 3984,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"hgvs_c": "n.999C>G",
"hgvs_p": null,
"transcript": "ENST00000485963.5",
"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": 2301,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PI4KA",
"gene_hgnc_id": 8983,
"dbsnp": "rs764985938",
"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": 0.28910624980926514,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.051,
"revel_prediction": "Benign",
"alphamissense_score": 0.1212,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.27,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 4.004,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000255882.11",
"gene_symbol": "PI4KA",
"hgnc_id": 8983,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.912C>G",
"hgvs_p": "p.Ile304Met"
}
],
"clinvar_disease": "Long QT syndrome",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Long QT syndrome",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}