← 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: 17-61457626-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=61457626&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 61457626,
"ref": "T",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000644296.1",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala",
"transcript": "NM_001321120.2",
"protein_id": "NP_001308049.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 546,
"cds_start": 276,
"cds_end": null,
"cds_length": 1641,
"cdna_start": 435,
"cdna_end": null,
"cdna_length": 3394,
"mane_select": "ENST00000644296.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala",
"transcript": "ENST00000644296.1",
"protein_id": "ENSP00000495986.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 546,
"cds_start": 276,
"cds_end": null,
"cds_length": 1641,
"cdna_start": 435,
"cdna_end": null,
"cdna_length": 3394,
"mane_select": "NM_001321120.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala",
"transcript": "ENST00000240335.1",
"protein_id": "ENSP00000240335.1",
"transcript_support_level": 1,
"aa_start": 92,
"aa_end": null,
"aa_length": 545,
"cds_start": 276,
"cds_end": null,
"cds_length": 1638,
"cdna_start": 321,
"cdna_end": null,
"cdna_length": 2470,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala",
"transcript": "ENST00000642491.1",
"protein_id": "ENSP00000495714.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 546,
"cds_start": 276,
"cds_end": null,
"cds_length": 1641,
"cdna_start": 303,
"cdna_end": null,
"cdna_length": 2149,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala",
"transcript": "NM_018488.3",
"protein_id": "NP_060958.2",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 545,
"cds_start": 276,
"cds_end": null,
"cds_length": 1638,
"cdna_start": 279,
"cdna_end": null,
"cdna_length": 3235,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.18T>G",
"hgvs_p": "p.Ala6Ala",
"transcript": "ENST00000589003.5",
"protein_id": "ENSP00000467588.1",
"transcript_support_level": 3,
"aa_start": 6,
"aa_end": null,
"aa_length": 134,
"cds_start": 18,
"cds_end": null,
"cds_length": 405,
"cdna_start": 197,
"cdna_end": null,
"cdna_length": 584,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.465T>G",
"hgvs_p": "p.Ala155Ala",
"transcript": "XM_011525490.3",
"protein_id": "XP_011523792.1",
"transcript_support_level": null,
"aa_start": 155,
"aa_end": null,
"aa_length": 609,
"cds_start": 465,
"cds_end": null,
"cds_length": 1830,
"cdna_start": 482,
"cdna_end": null,
"cdna_length": 3441,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.465T>G",
"hgvs_p": "p.Ala155Ala",
"transcript": "XM_011525491.3",
"protein_id": "XP_011523793.1",
"transcript_support_level": null,
"aa_start": 155,
"aa_end": null,
"aa_length": 608,
"cds_start": 465,
"cds_end": null,
"cds_length": 1827,
"cdna_start": 482,
"cdna_end": null,
"cdna_length": 3438,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "A",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"hgvs_c": "c.465T>G",
"hgvs_p": "p.Ala155Ala",
"transcript": "XM_011525495.3",
"protein_id": "XP_011523797.1",
"transcript_support_level": null,
"aa_start": 155,
"aa_end": null,
"aa_length": 417,
"cds_start": 465,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 484,
"cdna_end": null,
"cdna_length": 1705,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "LOC124904042",
"gene_hgnc_id": null,
"hgvs_c": "n.1077A>C",
"hgvs_p": null,
"transcript": "XR_007065872.1",
"protein_id": null,
"transcript_support_level": null,
"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": 5461,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "TBX4",
"gene_hgnc_id": 11603,
"dbsnp": "rs3744447",
"frequency_reference_population": 0.17299758,
"hom_count_reference_population": 26116,
"allele_count_reference_population": 278997,
"gnomad_exomes_af": 0.173653,
"gnomad_genomes_af": 0.166684,
"gnomad_exomes_ac": 253722,
"gnomad_genomes_ac": 25275,
"gnomad_exomes_homalt": 23737,
"gnomad_genomes_homalt": 2379,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.47999998927116394,
"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": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.106,
"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": -21,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
"acmg_by_gene": [
{
"score": -21,
"benign_score": 21,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000644296.1",
"gene_symbol": "TBX4",
"hgnc_id": 11603,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.276T>G",
"hgvs_p": "p.Ala92Ala"
},
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "XR_007065872.1",
"gene_symbol": "LOC124904042",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.1077A>C",
"hgvs_p": null
}
],
"clinvar_disease": "Coxopodopatellar syndrome,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:5",
"phenotype_combined": "Coxopodopatellar syndrome|not specified|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}