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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: M-8993-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=M&pos=8993&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "M",
"pos": 8993,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000361899.2",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 1,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MT-ATP6",
"gene_hgnc_id": 7414,
"hgvs_c": "c.467T>G",
"hgvs_p": "p.Leu156Arg",
"transcript": "ENST00000361899.2",
"protein_id": "ENSP00000354632.2",
"transcript_support_level": 6,
"aa_start": 156,
"aa_end": null,
"aa_length": 226,
"cds_start": 467,
"cds_end": null,
"cds_length": 681,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000361899.2"
},
{
"aa_ref": "L",
"aa_alt": "R",
"canonical": null,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 1,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP6",
"gene_hgnc_id": 7414,
"hgvs_c": "c.467T>G",
"hgvs_p": "p.Leu156Arg",
"transcript": "unassigned_transcript_4805",
"protein_id": null,
"transcript_support_level": null,
"aa_start": 156,
"aa_end": null,
"aa_length": 226,
"cds_start": 467,
"cds_end": null,
"cds_length": 681,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "unassigned_transcript_4805"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 1,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MT-CO3",
"gene_hgnc_id": 7422,
"hgvs_c": "c.-214T>G",
"hgvs_p": null,
"transcript": "ENST00000362079.2",
"protein_id": "ENSP00000354982.2",
"transcript_support_level": 6,
"aa_start": null,
"aa_end": null,
"aa_length": 260,
"cds_start": null,
"cds_end": null,
"cds_length": 784,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000362079.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": null,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 1,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COX3",
"gene_hgnc_id": 7422,
"hgvs_c": "c.-214T>G",
"hgvs_p": null,
"transcript": "unassigned_transcript_4806",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 260,
"cds_start": null,
"cds_end": null,
"cds_length": 784,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "unassigned_transcript_4806"
}
],
"gene_symbol": "MT-ATP6",
"gene_hgnc_id": 7414,
"dbsnp": "rs199476133",
"frequency_reference_population": null,
"hom_count_reference_population": null,
"allele_count_reference_population": null,
"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": 0.9739313125610352,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "Apogee2",
"splice_score_selected": null,
"splice_prediction_selected": null,
"splice_source_selected": null,
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": 0.9212,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 5.929,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": null,
"spliceai_max_prediction": null,
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": 0.9739313125610352,
"apogee2_prediction": "Pathogenic",
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 15,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PS4,PP1_Moderate,PS3_Supporting,PM5,PP3,PM2_Supporting,PM6_Strong",
"acmg_by_gene": [
{
"score": 15,
"benign_score": 0,
"pathogenic_score": 15,
"criteria": [
"PS4",
"PP1_Moderate",
"PS3_Supporting",
"PM5",
"PP3",
"PM2_Supporting",
"PM6_Strong"
],
"verdict": "Pathogenic",
"transcript": "ENST00000361899.2",
"gene_symbol": "MT-ATP6",
"hgnc_id": 7414,
"effects": [
"missense_variant"
],
"inheritance_mode": "Mitochondrial,AD,AR",
"hgvs_c": "c.467T>G",
"hgvs_p": "p.Leu156Arg"
},
{
"score": 15,
"benign_score": 0,
"pathogenic_score": 15,
"criteria": [
"PS4",
"PP1_Moderate",
"PS3_Supporting",
"PM5",
"PP3",
"PM2_Supporting",
"PM6_Strong"
],
"verdict": "Pathogenic",
"transcript": "unassigned_transcript_4805",
"gene_symbol": "ATP6",
"hgnc_id": 7414,
"effects": [
"missense_variant"
],
"inheritance_mode": "Mitochondrial,AD,AR",
"hgvs_c": "c.467T>G",
"hgvs_p": "p.Leu156Arg"
},
{
"score": 15,
"benign_score": 0,
"pathogenic_score": 15,
"criteria": [
"PS4",
"PP1_Moderate",
"PS3_Supporting",
"PM5",
"PP3",
"PM2_Supporting",
"PM6_Strong"
],
"verdict": "Pathogenic",
"transcript": "ENST00000362079.2",
"gene_symbol": "MT-CO3",
"hgnc_id": 7422,
"effects": [
"upstream_gene_variant"
],
"inheritance_mode": "Mitochondrial,AD,AR",
"hgvs_c": "c.-214T>G",
"hgvs_p": null
},
{
"score": 15,
"benign_score": 0,
"pathogenic_score": 15,
"criteria": [
"PS4",
"PP1_Moderate",
"PS3_Supporting",
"PM5",
"PP3",
"PM2_Supporting",
"PM6_Strong"
],
"verdict": "Pathogenic",
"transcript": "unassigned_transcript_4806",
"gene_symbol": "COX3",
"hgnc_id": 7422,
"effects": [
"upstream_gene_variant"
],
"inheritance_mode": "Mitochondrial,AD,AR",
"hgvs_c": "c.-214T>G",
"hgvs_p": null
}
],
"clinvar_disease": " infantile, mitochondrial, mitochondrial type 1,8 conditions,Cerebellar ataxia,Leber optic atrophy,Leigh syndrome,Mitochondrial complex 5 (ATP synthase) deficiency,Mitochondrial disease,NARP syndrome,Rod-cone dystrophy,Striatonigral degeneration,not provided,not specified",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "reviewed by expert panel",
"clinvar_submissions_summary": "P:16 LP:1 O:1",
"phenotype_combined": "NARP-/-Leigh-Disease-/-MILS-/-other,NARP-/-Leigh-Disease-/-MILS-/-other,Leigh syndrome|NARP syndrome|Cerebellar ataxia|not provided|Mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1|8 conditions|Mitochondrial disease|Rod-cone dystrophy|Leber optic atrophy|not specified|Striatonigral degeneration, infantile, mitochondrial",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}