← Back to variant description
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: 19-52283338-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=52283338&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 52283338,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001010851.3",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.199C>T",
"hgvs_p": "p.Pro67Ser",
"transcript": "NM_001010851.3",
"protein_id": "NP_001010851.1",
"transcript_support_level": null,
"aa_start": 67,
"aa_end": null,
"aa_length": 468,
"cds_start": 199,
"cds_end": null,
"cds_length": 1407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000439461.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001010851.3"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.199C>T",
"hgvs_p": "p.Pro67Ser",
"transcript": "ENST00000439461.6",
"protein_id": "ENSP00000409652.1",
"transcript_support_level": 1,
"aa_start": 67,
"aa_end": null,
"aa_length": 468,
"cds_start": 199,
"cds_end": null,
"cds_length": 1407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001010851.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000439461.6"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.229C>T",
"hgvs_p": "p.Pro77Ser",
"transcript": "ENST00000950441.1",
"protein_id": "ENSP00000620500.1",
"transcript_support_level": null,
"aa_start": 77,
"aa_end": null,
"aa_length": 478,
"cds_start": 229,
"cds_end": null,
"cds_length": 1437,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950441.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.244C>T",
"hgvs_p": "p.Pro82Ser",
"transcript": "ENST00000593612.1",
"protein_id": "ENSP00000468950.1",
"transcript_support_level": 2,
"aa_start": 82,
"aa_end": null,
"aa_length": 471,
"cds_start": 244,
"cds_end": null,
"cds_length": 1416,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000593612.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.22C>T",
"hgvs_p": "p.Pro8Ser",
"transcript": "ENST00000593703.1",
"protein_id": "ENSP00000469186.1",
"transcript_support_level": 4,
"aa_start": 8,
"aa_end": null,
"aa_length": 158,
"cds_start": 22,
"cds_end": null,
"cds_length": 477,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000593703.1"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.88C>T",
"hgvs_p": "p.Pro30Ser",
"transcript": "ENST00000595000.5",
"protein_id": "ENSP00000472041.1",
"transcript_support_level": 4,
"aa_start": 30,
"aa_end": null,
"aa_length": 114,
"cds_start": 88,
"cds_end": null,
"cds_length": 345,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000595000.5"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.199C>T",
"hgvs_p": "p.Pro67Ser",
"transcript": "ENST00000599581.5",
"protein_id": "ENSP00000471965.1",
"transcript_support_level": 2,
"aa_start": 67,
"aa_end": null,
"aa_length": 105,
"cds_start": 199,
"cds_end": null,
"cds_length": 318,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000599581.5"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.184C>T",
"hgvs_p": "p.Pro62Ser",
"transcript": "ENST00000600821.5",
"protein_id": "ENSP00000472708.1",
"transcript_support_level": 4,
"aa_start": 62,
"aa_end": null,
"aa_length": 100,
"cds_start": 184,
"cds_end": null,
"cds_length": 303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000600821.5"
},
{
"aa_ref": "P",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.88C>T",
"hgvs_p": "p.Pro30Ser",
"transcript": "ENST00000595149.5",
"protein_id": "ENSP00000471620.1",
"transcript_support_level": 4,
"aa_start": 30,
"aa_end": null,
"aa_length": 82,
"cds_start": 88,
"cds_end": null,
"cds_length": 251,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000595149.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"hgvs_c": "c.*20C>T",
"hgvs_p": null,
"transcript": "ENST00000601711.5",
"protein_id": "ENSP00000472743.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 73,
"cds_start": null,
"cds_end": null,
"cds_length": 224,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000601711.5"
}
],
"gene_symbol": "ZNF766",
"gene_hgnc_id": 28063,
"dbsnp": "rs1333929287",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"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": 0.06368279457092285,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.037,
"revel_prediction": "Benign",
"alphamissense_score": 0.4239,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.63,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.301,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_001010851.3",
"gene_symbol": "ZNF766",
"hgnc_id": 28063,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.199C>T",
"hgvs_p": "p.Pro67Ser"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}