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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: 17-75835666-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=75835666&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 75835666,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_199242.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser",
"transcript": "NM_199242.3",
"protein_id": "NP_954712.1",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 1090,
"cds_start": 1708,
"cds_end": null,
"cds_length": 3273,
"cdna_start": 1775,
"cdna_end": null,
"cdna_length": 4080,
"mane_select": "ENST00000207549.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_199242.3"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser",
"transcript": "ENST00000207549.9",
"protein_id": "ENSP00000207549.3",
"transcript_support_level": 1,
"aa_start": 570,
"aa_end": null,
"aa_length": 1090,
"cds_start": 1708,
"cds_end": null,
"cds_length": 3273,
"cdna_start": 1775,
"cdna_end": null,
"cdna_length": 4080,
"mane_select": "NM_199242.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000207549.9"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser",
"transcript": "ENST00000412096.6",
"protein_id": "ENSP00000388093.1",
"transcript_support_level": 2,
"aa_start": 570,
"aa_end": null,
"aa_length": 1142,
"cds_start": 1708,
"cds_end": null,
"cds_length": 3429,
"cdna_start": 1721,
"cdna_end": null,
"cdna_length": 3648,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000412096.6"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser",
"transcript": "ENST00000868100.1",
"protein_id": "ENSP00000538159.1",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 1090,
"cds_start": 1708,
"cds_end": null,
"cds_length": 3273,
"cdna_start": 1779,
"cdna_end": null,
"cdna_length": 4084,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868100.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser",
"transcript": "ENST00000868101.1",
"protein_id": "ENSP00000538160.1",
"transcript_support_level": null,
"aa_start": 570,
"aa_end": null,
"aa_length": 1090,
"cds_start": 1708,
"cds_end": null,
"cds_length": 3273,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 4078,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000868101.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1657C>A",
"hgvs_p": "p.Arg553Ser",
"transcript": "ENST00000965711.1",
"protein_id": "ENSP00000635770.1",
"transcript_support_level": null,
"aa_start": 553,
"aa_end": null,
"aa_length": 1073,
"cds_start": 1657,
"cds_end": null,
"cds_length": 3222,
"cdna_start": 1752,
"cdna_end": null,
"cdna_length": 4057,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000965711.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.1615C>A",
"hgvs_p": "p.Arg539Ser",
"transcript": "ENST00000965712.1",
"protein_id": "ENSP00000635771.1",
"transcript_support_level": null,
"aa_start": 539,
"aa_end": null,
"aa_length": 1059,
"cds_start": 1615,
"cds_end": null,
"cds_length": 3180,
"cdna_start": 1996,
"cdna_end": null,
"cdna_length": 4301,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000965712.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.643C>A",
"hgvs_p": "p.Arg215Ser",
"transcript": "ENST00000699510.1",
"protein_id": "ENSP00000514405.1",
"transcript_support_level": null,
"aa_start": 215,
"aa_end": null,
"aa_length": 712,
"cds_start": 643,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 643,
"cdna_end": null,
"cdna_length": 2740,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699510.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.883C>A",
"hgvs_p": "p.Arg295Ser",
"transcript": "ENST00000699511.1",
"protein_id": "ENSP00000514406.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 297,
"cds_start": 883,
"cds_end": null,
"cds_length": 896,
"cdna_start": 885,
"cdna_end": null,
"cdna_length": 898,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000699511.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "c.436C>A",
"hgvs_p": "p.Arg146Ser",
"transcript": "ENST00000586147.1",
"protein_id": "ENSP00000466543.1",
"transcript_support_level": 5,
"aa_start": 146,
"aa_end": null,
"aa_length": 187,
"cds_start": 436,
"cds_end": null,
"cds_length": 566,
"cdna_start": 459,
"cdna_end": null,
"cdna_length": 589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000586147.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "n.1978C>A",
"hgvs_p": null,
"transcript": "ENST00000591563.5",
"protein_id": null,
"transcript_support_level": 2,
"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": 4382,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000591563.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"hgvs_c": "n.*384C>A",
"hgvs_p": null,
"transcript": "ENST00000587105.1",
"protein_id": "ENSP00000466377.1",
"transcript_support_level": 3,
"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": 776,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000587105.1"
}
],
"gene_symbol": "UNC13D",
"gene_hgnc_id": 23147,
"dbsnp": "rs549768303",
"frequency_reference_population": 6.844627e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84463e-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": 0.10562187433242798,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.076,
"revel_prediction": "Benign",
"alphamissense_score": 0.1198,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.51,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.421,
"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": 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_199242.3",
"gene_symbol": "UNC13D",
"hgnc_id": 23147,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1708C>A",
"hgvs_p": "p.Arg570Ser"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}