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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: 19-6669936-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=6669936&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 6669936,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_003807.5",
"consequences": [
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "NM_001376887.1",
"protein_id": "NP_001363816.1",
"transcript_support_level": null,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000675206.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001376887.1"
},
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "ENST00000675206.1",
"protein_id": "ENSP00000502837.1",
"transcript_support_level": null,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001376887.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000675206.1"
},
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "ENST00000599359.1",
"protein_id": "ENSP00000469049.1",
"transcript_support_level": 1,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000599359.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.111+23T>C",
"hgvs_p": null,
"transcript": "ENST00000245912.7",
"protein_id": "ENSP00000245912.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 204,
"cds_start": null,
"cds_end": null,
"cds_length": 615,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000245912.7"
},
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "NM_003807.5",
"protein_id": "NP_003798.2",
"transcript_support_level": null,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003807.5"
},
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "ENST00000896417.1",
"protein_id": "ENSP00000566476.1",
"transcript_support_level": null,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896417.1"
},
{
"aa_ref": "L",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser",
"transcript": "ENST00000896418.1",
"protein_id": "ENSP00000566477.1",
"transcript_support_level": null,
"aa_start": 45,
"aa_end": null,
"aa_length": 240,
"cds_start": 134,
"cds_end": null,
"cds_length": 723,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896418.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "c.111+23T>C",
"hgvs_p": null,
"transcript": "NM_172014.3",
"protein_id": "NP_742011.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 204,
"cds_start": null,
"cds_end": null,
"cds_length": 615,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_172014.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"hgvs_c": "n.134T>C",
"hgvs_p": null,
"transcript": "ENST00000850589.1",
"protein_id": "ENSP00000520876.1",
"transcript_support_level": null,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000850589.1"
}
],
"gene_symbol": "TNFSF14",
"gene_hgnc_id": 11930,
"dbsnp": "rs757186501",
"frequency_reference_population": 0.000063823725,
"hom_count_reference_population": 0,
"allele_count_reference_population": 103,
"gnomad_exomes_af": 0.0000697738,
"gnomad_genomes_af": 0.00000658094,
"gnomad_exomes_ac": 102,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.4033771753311157,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.136,
"revel_prediction": "Benign",
"alphamissense_score": 0.1913,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.39,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.075,
"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": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 1,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "NM_003807.5",
"gene_symbol": "TNFSF14",
"hgnc_id": 11930,
"effects": [
"missense_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.134T>C",
"hgvs_p": "p.Leu45Ser"
}
],
"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
}