← 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: 15-62819540-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=62819540&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 62819540,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000636159.2",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 53,
"exon_rank_end": null,
"exon_count": 59,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "c.6796T>G",
"hgvs_p": "p.Phe2266Val",
"transcript": "NM_015059.3",
"protein_id": "NP_055874.2",
"transcript_support_level": null,
"aa_start": 2266,
"aa_end": null,
"aa_length": 2542,
"cds_start": 6796,
"cds_end": null,
"cds_length": 7629,
"cdna_start": 7169,
"cdna_end": null,
"cdna_length": 12023,
"mane_select": "ENST00000636159.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 53,
"exon_rank_end": null,
"exon_count": 59,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "c.6796T>G",
"hgvs_p": "p.Phe2266Val",
"transcript": "ENST00000636159.2",
"protein_id": "ENSP00000490662.2",
"transcript_support_level": 5,
"aa_start": 2266,
"aa_end": null,
"aa_length": 2542,
"cds_start": 6796,
"cds_end": null,
"cds_length": 7629,
"cdna_start": 7169,
"cdna_end": null,
"cdna_length": 12023,
"mane_select": "NM_015059.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "n.4711T>G",
"hgvs_p": null,
"transcript": "ENST00000489129.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 6420,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 52,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "c.6796T>G",
"hgvs_p": "p.Phe2266Val",
"transcript": "NM_001394547.1",
"protein_id": "NP_001381476.1",
"transcript_support_level": null,
"aa_start": 2266,
"aa_end": null,
"aa_length": 2542,
"cds_start": 6796,
"cds_end": null,
"cds_length": 7629,
"cdna_start": 7044,
"cdna_end": null,
"cdna_length": 11898,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 52,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "c.6796T>G",
"hgvs_p": "p.Phe2266Val",
"transcript": "ENST00000561311.5",
"protein_id": "ENSP00000453508.1",
"transcript_support_level": 5,
"aa_start": 2266,
"aa_end": null,
"aa_length": 2542,
"cds_start": 6796,
"cds_end": null,
"cds_length": 7629,
"cdna_start": 7026,
"cdna_end": null,
"cdna_length": 11880,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"hgvs_c": "c.3538T>G",
"hgvs_p": "p.Phe1180Val",
"transcript": "ENST00000494733.5",
"protein_id": "ENSP00000453730.1",
"transcript_support_level": 5,
"aa_start": 1180,
"aa_end": null,
"aa_length": 1471,
"cds_start": 3538,
"cds_end": null,
"cds_length": 4416,
"cdna_start": 3538,
"cdna_end": null,
"cdna_length": 5155,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "TLN2",
"gene_hgnc_id": 15447,
"dbsnp": "rs3816988",
"frequency_reference_population": 0.00002540301,
"hom_count_reference_population": 0,
"allele_count_reference_population": 41,
"gnomad_exomes_af": 0.0000253116,
"gnomad_genomes_af": 0.0000262809,
"gnomad_exomes_ac": 37,
"gnomad_genomes_ac": 4,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.11391925811767578,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.043,
"revel_prediction": "Benign",
"alphamissense_score": 0.071,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.47,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.019,
"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": -6,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate,BS2",
"acmg_by_gene": [
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000636159.2",
"gene_symbol": "TLN2",
"hgnc_id": 15447,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.6796T>G",
"hgvs_p": "p.Phe2266Val"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}