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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: 11-110136996-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=110136996&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 110136996,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_033390.2",
"consequences": [
{
"aa_ref": "Q",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"hgvs_c": "c.355C>G",
"hgvs_p": "p.Gln119Glu",
"transcript": "NM_033390.2",
"protein_id": "NP_203748.1",
"transcript_support_level": null,
"aa_start": 119,
"aa_end": null,
"aa_length": 883,
"cds_start": 355,
"cds_end": null,
"cds_length": 2652,
"cdna_start": 375,
"cdna_end": null,
"cdna_length": 8776,
"mane_select": "ENST00000278590.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"hgvs_c": "c.355C>G",
"hgvs_p": "p.Gln119Glu",
"transcript": "ENST00000278590.8",
"protein_id": "ENSP00000278590.3",
"transcript_support_level": 2,
"aa_start": 119,
"aa_end": null,
"aa_length": 883,
"cds_start": 355,
"cds_end": null,
"cds_length": 2652,
"cdna_start": 375,
"cdna_end": null,
"cdna_length": 8776,
"mane_select": "NM_033390.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"hgvs_c": "c.358C>G",
"hgvs_p": "p.Gln120Glu",
"transcript": "NM_001411037.1",
"protein_id": "NP_001397966.1",
"transcript_support_level": null,
"aa_start": 120,
"aa_end": null,
"aa_length": 884,
"cds_start": 358,
"cds_end": null,
"cds_length": 2655,
"cdna_start": 441,
"cdna_end": null,
"cdna_length": 8842,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"hgvs_c": "c.358C>G",
"hgvs_p": "p.Gln120Glu",
"transcript": "ENST00000528673.5",
"protein_id": "ENSP00000431821.1",
"transcript_support_level": 2,
"aa_start": 120,
"aa_end": null,
"aa_length": 884,
"cds_start": 358,
"cds_end": null,
"cds_length": 2655,
"cdna_start": 437,
"cdna_end": null,
"cdna_length": 2931,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"hgvs_c": "c.262C>G",
"hgvs_p": "p.Gln88Glu",
"transcript": "ENST00000453089.2",
"protein_id": "ENSP00000413094.2",
"transcript_support_level": 2,
"aa_start": 88,
"aa_end": null,
"aa_length": 852,
"cds_start": 262,
"cds_end": null,
"cds_length": 2559,
"cdna_start": 1143,
"cdna_end": null,
"cdna_length": 9542,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "RDX",
"gene_hgnc_id": 9944,
"hgvs_c": "n.*251-5266G>C",
"hgvs_p": null,
"transcript": "ENST00000645527.1",
"protein_id": "ENSP00000496121.1",
"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": 3239,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "ZC3H12C",
"gene_hgnc_id": 29362,
"dbsnp": "rs775161683",
"frequency_reference_population": 0.000013139396,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": null,
"gnomad_genomes_af": 0.0000131394,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.11782443523406982,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.113,
"revel_prediction": "Benign",
"alphamissense_score": 0.1326,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.3,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.631,
"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": 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_033390.2",
"gene_symbol": "ZC3H12C",
"hgnc_id": 29362,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.355C>G",
"hgvs_p": "p.Gln119Glu"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000645527.1",
"gene_symbol": "RDX",
"hgnc_id": 9944,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "n.*251-5266G>C",
"hgvs_p": null
}
],
"clinvar_disease": "X-linked Alport syndrome",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "X-linked Alport syndrome",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}