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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: X-118641602-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=118641602&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 118641602,
"ref": "T",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000276202.9",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4260+297T>G",
"hgvs_p": null,
"transcript": "NM_144658.4",
"protein_id": "NP_653259.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2073,
"cds_start": -4,
"cds_end": null,
"cds_length": 6222,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6719,
"mane_select": "ENST00000276202.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4260+297T>G",
"hgvs_p": null,
"transcript": "ENST00000276202.9",
"protein_id": "ENSP00000276202.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2073,
"cds_start": -4,
"cds_end": null,
"cds_length": 6222,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6719,
"mane_select": "NM_144658.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4260+297T>G",
"hgvs_p": null,
"transcript": "ENST00000276204.10",
"protein_id": "ENSP00000276204.6",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 2077,
"cds_start": -4,
"cds_end": null,
"cds_length": 6234,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6664,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 49,
"intron_rank": 35,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.3747+297T>G",
"hgvs_p": null,
"transcript": "ENST00000633080.1",
"protein_id": "ENSP00000487829.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1902,
"cds_start": -4,
"cds_end": null,
"cds_length": 5709,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6041,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4299+297T>G",
"hgvs_p": null,
"transcript": "XM_005262368.5",
"protein_id": "XP_005262425.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2086,
"cds_start": -4,
"cds_end": null,
"cds_length": 6261,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6758,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4227+297T>G",
"hgvs_p": null,
"transcript": "XM_011531276.4",
"protein_id": "XP_011529578.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2062,
"cds_start": -4,
"cds_end": null,
"cds_length": 6189,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6806,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": 40,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4206+297T>G",
"hgvs_p": null,
"transcript": "XM_005262369.6",
"protein_id": "XP_005262426.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2055,
"cds_start": -4,
"cds_end": null,
"cds_length": 6168,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 11935,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": 39,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.4167+297T>G",
"hgvs_p": null,
"transcript": "XM_047441841.1",
"protein_id": "XP_047297797.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2042,
"cds_start": -4,
"cds_end": null,
"cds_length": 6129,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 11896,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": 27,
"intron_rank_end": null,
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"hgvs_c": "c.2415+297T>G",
"hgvs_p": null,
"transcript": "XM_011531278.3",
"protein_id": "XP_011529580.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1458,
"cds_start": -4,
"cds_end": null,
"cds_length": 4377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "DOCK11",
"gene_hgnc_id": 23483,
"dbsnp": "rs17326758",
"frequency_reference_population": 0.098045565,
"hom_count_reference_population": 3785,
"allele_count_reference_population": 10901,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.0980456,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 10901,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 477,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.8399999737739563,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.84,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.055,
"phylop100way_prediction": "Benign",
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000276202.9",
"gene_symbol": "DOCK11",
"hgnc_id": 23483,
"effects": [
"intron_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "c.4260+297T>G",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}