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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: 22-23767438-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=23767438&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 23767438,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000484558.3",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "c.197G>A",
"hgvs_p": "p.Gly66Asp",
"transcript": "NM_213720.3",
"protein_id": "NP_998885.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 142,
"cds_start": 197,
"cds_end": null,
"cds_length": 429,
"cdna_start": 295,
"cdna_end": null,
"cdna_length": 700,
"mane_select": "ENST00000484558.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "c.197G>A",
"hgvs_p": "p.Gly66Asp",
"transcript": "ENST00000484558.3",
"protein_id": "ENSP00000418428.3",
"transcript_support_level": 1,
"aa_start": 66,
"aa_end": null,
"aa_length": 142,
"cds_start": 197,
"cds_end": null,
"cds_length": 429,
"cdna_start": 295,
"cdna_end": null,
"cdna_length": 700,
"mane_select": "NM_213720.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "c.197G>A",
"hgvs_p": "p.Gly66Asp",
"transcript": "NM_001301339.2",
"protein_id": "NP_001288268.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 149,
"cds_start": 197,
"cds_end": null,
"cds_length": 450,
"cdna_start": 295,
"cdna_end": null,
"cdna_length": 721,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "c.197G>A",
"hgvs_p": "p.Gly66Asp",
"transcript": "ENST00000401675.7",
"protein_id": "ENSP00000384973.3",
"transcript_support_level": 5,
"aa_start": 66,
"aa_end": null,
"aa_length": 149,
"cds_start": 197,
"cds_end": null,
"cds_length": 450,
"cdna_start": 265,
"cdna_end": null,
"cdna_length": 691,
"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": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "n.144G>A",
"hgvs_p": null,
"transcript": "ENST00000517886.1",
"protein_id": "ENSP00000429976.1",
"transcript_support_level": 3,
"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": 494,
"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": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "n.242G>A",
"hgvs_p": null,
"transcript": "NR_125755.2",
"protein_id": null,
"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": 647,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "c.41+396G>A",
"hgvs_p": null,
"transcript": "ENST00000520222.1",
"protein_id": "ENSP00000430042.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 55,
"cds_start": -4,
"cds_end": null,
"cds_length": 168,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 384,
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"hgvs_c": "n.139+396G>A",
"hgvs_p": null,
"transcript": "NR_125756.2",
"protein_id": null,
"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": 480,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CHCHD10",
"gene_hgnc_id": 15559,
"dbsnp": "rs730880031",
"frequency_reference_population": 6.883222e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.88322e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.854243278503418,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.613,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.9896,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.22,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 5.757,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.03,
"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": 8,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PM1,PM2,PM5,PP3_Moderate",
"acmg_by_gene": [
{
"score": 8,
"benign_score": 0,
"pathogenic_score": 8,
"criteria": [
"PM1",
"PM2",
"PM5",
"PP3_Moderate"
],
"verdict": "Likely_pathogenic",
"transcript": "ENST00000484558.3",
"gene_symbol": "CHCHD10",
"hgnc_id": 15559,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.197G>A",
"hgvs_p": "p.Gly66Asp"
}
],
"clinvar_disease": "Autosomal dominant mitochondrial myopathy with exercise intolerance,Frontotemporal dementia and/or amyotrophic lateral sclerosis 2,Lower motor neuron syndrome with late-adult onset",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Lower motor neuron syndrome with late-adult onset;Autosomal dominant mitochondrial myopathy with exercise intolerance;Frontotemporal dementia and/or amyotrophic lateral sclerosis 2",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}