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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: 18-74781491-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=74781491&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "18",
"pos": 74781491,
"ref": "C",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "NM_017757.3",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "NM_017757.3",
"protein_id": "NP_060227.2",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 2248,
"cds_start": 4866,
"cds_end": null,
"cds_length": 6747,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000299687.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_017757.3"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "ENST00000299687.10",
"protein_id": "ENSP00000299687.4",
"transcript_support_level": 1,
"aa_start": 1622,
"aa_end": null,
"aa_length": 2248,
"cds_start": 4866,
"cds_end": null,
"cds_length": 6747,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_017757.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000299687.10"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "NM_001384475.1",
"protein_id": "NP_001371404.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 2248,
"cds_start": 4866,
"cds_end": null,
"cds_length": 6747,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001384475.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "NM_001146189.1",
"protein_id": "NP_001139661.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1815,
"cds_start": 4866,
"cds_end": null,
"cds_length": 5448,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001146189.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "ENST00000577538.5",
"protein_id": "ENSP00000463270.1",
"transcript_support_level": 2,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1815,
"cds_start": 4866,
"cds_end": null,
"cds_length": 5448,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000577538.5"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.3222C>A",
"hgvs_p": "p.Thr1074Thr",
"transcript": "ENST00000949102.1",
"protein_id": "ENSP00000619161.1",
"transcript_support_level": null,
"aa_start": 1074,
"aa_end": null,
"aa_length": 1700,
"cds_start": 3222,
"cds_end": null,
"cds_length": 5103,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949102.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "NM_001146190.1",
"protein_id": "NP_001139662.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1660,
"cds_start": 4866,
"cds_end": null,
"cds_length": 4983,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001146190.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "ENST00000309902.10",
"protein_id": "ENSP00000310359.5",
"transcript_support_level": 2,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1660,
"cds_start": 4866,
"cds_end": null,
"cds_length": 4983,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000309902.10"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "ENST00000582337.5",
"protein_id": "ENSP00000462348.1",
"transcript_support_level": 5,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1660,
"cds_start": 4866,
"cds_end": null,
"cds_length": 4983,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000582337.5"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.276C>A",
"hgvs_p": "p.Thr92Thr",
"transcript": "ENST00000949101.1",
"protein_id": "ENSP00000619160.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 718,
"cds_start": 276,
"cds_end": null,
"cds_length": 2157,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949101.1"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "XM_017025838.3",
"protein_id": "XP_016881327.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1750,
"cds_start": 4866,
"cds_end": null,
"cds_length": 5253,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017025838.3"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "XM_011526069.4",
"protein_id": "XP_011524371.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1688,
"cds_start": 4866,
"cds_end": null,
"cds_length": 5067,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526069.4"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "XM_011526070.3",
"protein_id": "XP_011524372.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1660,
"cds_start": 4866,
"cds_end": null,
"cds_length": 4983,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526070.3"
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr",
"transcript": "XM_006722500.5",
"protein_id": "XP_006722563.1",
"transcript_support_level": null,
"aa_start": 1622,
"aa_end": null,
"aa_length": 1630,
"cds_start": 4866,
"cds_end": null,
"cds_length": 4893,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006722500.5"
}
],
"gene_symbol": "ZNF407",
"gene_hgnc_id": 19904,
"dbsnp": "rs752545983",
"frequency_reference_population": 7.320848e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 7.32085e-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": -0.17000000178813934,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.17,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.306,
"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,BP7",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4",
"BP7"
],
"verdict": "Uncertain_significance",
"transcript": "NM_017757.3",
"gene_symbol": "ZNF407",
"hgnc_id": 19904,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.4866C>A",
"hgvs_p": "p.Thr1622Thr"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}