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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: 8-25861178-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=25861178&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "8",
"pos": 25861178,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_022659.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.1213G>T",
"hgvs_p": "p.Val405Phe",
"transcript": "NM_022659.4",
"protein_id": "NP_073150.2",
"transcript_support_level": null,
"aa_start": 405,
"aa_end": null,
"aa_length": 575,
"cds_start": 1213,
"cds_end": null,
"cds_length": 1728,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000520164.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_022659.4"
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.1213G>T",
"hgvs_p": "p.Val405Phe",
"transcript": "ENST00000520164.6",
"protein_id": "ENSP00000430241.1",
"transcript_support_level": 2,
"aa_start": 405,
"aa_end": null,
"aa_length": 575,
"cds_start": 1213,
"cds_end": null,
"cds_length": 1728,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_022659.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000520164.6"
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.1213G>T",
"hgvs_p": "p.Val405Phe",
"transcript": "ENST00000965179.1",
"protein_id": "ENSP00000635238.1",
"transcript_support_level": null,
"aa_start": 405,
"aa_end": null,
"aa_length": 553,
"cds_start": 1213,
"cds_end": null,
"cds_length": 1662,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000965179.1"
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.862G>T",
"hgvs_p": "p.Val288Phe",
"transcript": "ENST00000901147.1",
"protein_id": "ENSP00000571206.1",
"transcript_support_level": null,
"aa_start": 288,
"aa_end": null,
"aa_length": 458,
"cds_start": 862,
"cds_end": null,
"cds_length": 1377,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000901147.1"
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.769G>T",
"hgvs_p": "p.Val257Phe",
"transcript": "ENST00000408929.7",
"protein_id": "ENSP00000386178.3",
"transcript_support_level": 2,
"aa_start": 257,
"aa_end": null,
"aa_length": 427,
"cds_start": 769,
"cds_end": null,
"cds_length": 1284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000408929.7"
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"hgvs_c": "c.406G>T",
"hgvs_p": "p.Val136Phe",
"transcript": "ENST00000535548.1",
"protein_id": "ENSP00000437909.1",
"transcript_support_level": 2,
"aa_start": 136,
"aa_end": null,
"aa_length": 264,
"cds_start": 406,
"cds_end": null,
"cds_length": 795,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000535548.1"
},
{
"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": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "LOC102723395",
"gene_hgnc_id": null,
"hgvs_c": "n.214-8801C>A",
"hgvs_p": null,
"transcript": "XR_001745848.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_001745848.2"
}
],
"gene_symbol": "EBF2",
"gene_hgnc_id": 19090,
"dbsnp": "rs369134736",
"frequency_reference_population": 0.000012314816,
"hom_count_reference_population": 0,
"allele_count_reference_population": 18,
"gnomad_exomes_af": 0.0000123148,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 18,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.7116806507110596,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.273,
"revel_prediction": "Benign",
"alphamissense_score": 0.2203,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.04,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 6.152,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BS2",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_022659.4",
"gene_symbol": "EBF2",
"hgnc_id": 19090,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1213G>T",
"hgvs_p": "p.Val405Phe"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "XR_001745848.2",
"gene_symbol": "LOC102723395",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.214-8801C>A",
"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
}