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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: 11-63143607-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=63143607&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 63143607,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000326192.5",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC22A24",
"gene_hgnc_id": 28542,
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser",
"transcript": "NM_001136506.2",
"protein_id": "NP_001129978.2",
"transcript_support_level": null,
"aa_start": 58,
"aa_end": null,
"aa_length": 552,
"cds_start": 173,
"cds_end": null,
"cds_length": 1659,
"cdna_start": 615,
"cdna_end": null,
"cdna_length": 2101,
"mane_select": "ENST00000612278.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC22A24",
"gene_hgnc_id": 28542,
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser",
"transcript": "ENST00000612278.4",
"protein_id": "ENSP00000480336.1",
"transcript_support_level": 5,
"aa_start": 58,
"aa_end": null,
"aa_length": 552,
"cds_start": 173,
"cds_end": null,
"cds_length": 1659,
"cdna_start": 615,
"cdna_end": null,
"cdna_length": 2101,
"mane_select": "NM_001136506.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SLC22A24",
"gene_hgnc_id": 28542,
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser",
"transcript": "ENST00000417740.5",
"protein_id": "ENSP00000396586.1",
"transcript_support_level": 5,
"aa_start": 58,
"aa_end": null,
"aa_length": 551,
"cds_start": 173,
"cds_end": null,
"cds_length": 1656,
"cdna_start": 615,
"cdna_end": null,
"cdna_length": 2098,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"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": "SLC22A24",
"gene_hgnc_id": 28542,
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser",
"transcript": "ENST00000326192.5",
"protein_id": "ENSP00000321549.5",
"transcript_support_level": 1,
"aa_start": 58,
"aa_end": null,
"aa_length": 322,
"cds_start": 173,
"cds_end": null,
"cds_length": 969,
"cdna_start": 615,
"cdna_end": null,
"cdna_length": 1663,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"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": "SLC22A24",
"gene_hgnc_id": 28542,
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser",
"transcript": "NM_173586.3",
"protein_id": "NP_775857.2",
"transcript_support_level": null,
"aa_start": 58,
"aa_end": null,
"aa_length": 322,
"cds_start": 173,
"cds_end": null,
"cds_length": 969,
"cdna_start": 615,
"cdna_end": null,
"cdna_length": 1663,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SLC22A24",
"gene_hgnc_id": 28542,
"dbsnp": "rs1939748",
"frequency_reference_population": 0.833827,
"hom_count_reference_population": 551601,
"allele_count_reference_population": 1312904,
"gnomad_exomes_af": 0.841692,
"gnomad_genomes_af": 0.760261,
"gnomad_exomes_ac": 1197282,
"gnomad_genomes_ac": 115622,
"gnomad_exomes_homalt": 506064,
"gnomad_genomes_homalt": 45537,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 9.052667451214802e-7,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.086,
"revel_prediction": "Benign",
"alphamissense_score": 0.1326,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.71,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.11,
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000326192.5",
"gene_symbol": "SLC22A24",
"hgnc_id": 28542,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.173C>G",
"hgvs_p": "p.Thr58Ser"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}