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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: 17-9635526-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=9635526&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 9635526,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000352665.10",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1442C>G",
"hgvs_p": "p.Thr481Ser",
"transcript": "NM_145054.5",
"protein_id": "NP_659491.4",
"transcript_support_level": null,
"aa_start": 481,
"aa_end": null,
"aa_length": 620,
"cds_start": 1442,
"cds_end": null,
"cds_length": 1863,
"cdna_start": 1496,
"cdna_end": null,
"cdna_length": 2166,
"mane_select": "ENST00000352665.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1442C>G",
"hgvs_p": "p.Thr481Ser",
"transcript": "ENST00000352665.10",
"protein_id": "ENSP00000339449.5",
"transcript_support_level": 1,
"aa_start": 481,
"aa_end": null,
"aa_length": 620,
"cds_start": 1442,
"cds_end": null,
"cds_length": 1863,
"cdna_start": 1496,
"cdna_end": null,
"cdna_length": 2166,
"mane_select": "NM_145054.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1238C>G",
"hgvs_p": "p.Thr413Ser",
"transcript": "NM_001080556.2",
"protein_id": "NP_001074025.1",
"transcript_support_level": null,
"aa_start": 413,
"aa_end": null,
"aa_length": 552,
"cds_start": 1238,
"cds_end": null,
"cds_length": 1659,
"cdna_start": 1292,
"cdna_end": null,
"cdna_length": 1962,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1238C>G",
"hgvs_p": "p.Thr413Ser",
"transcript": "ENST00000396219.7",
"protein_id": "ENSP00000379521.3",
"transcript_support_level": 2,
"aa_start": 413,
"aa_end": null,
"aa_length": 552,
"cds_start": 1238,
"cds_end": null,
"cds_length": 1659,
"cdna_start": 1307,
"cdna_end": null,
"cdna_length": 1912,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.95C>G",
"hgvs_p": "p.Thr32Ser",
"transcript": "ENST00000574097.1",
"protein_id": "ENSP00000468193.1",
"transcript_support_level": 3,
"aa_start": 32,
"aa_end": null,
"aa_length": 92,
"cds_start": 95,
"cds_end": null,
"cds_length": 279,
"cdna_start": 96,
"cdna_end": null,
"cdna_length": 597,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1442C>G",
"hgvs_p": "p.Thr481Ser",
"transcript": "XM_047435437.1",
"protein_id": "XP_047291393.1",
"transcript_support_level": null,
"aa_start": 481,
"aa_end": null,
"aa_length": 627,
"cds_start": 1442,
"cds_end": null,
"cds_length": 1884,
"cdna_start": 1496,
"cdna_end": null,
"cdna_length": 1938,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1238C>G",
"hgvs_p": "p.Thr413Ser",
"transcript": "XM_047435438.1",
"protein_id": "XP_047291394.1",
"transcript_support_level": null,
"aa_start": 413,
"aa_end": null,
"aa_length": 559,
"cds_start": 1238,
"cds_end": null,
"cds_length": 1680,
"cdna_start": 1292,
"cdna_end": null,
"cdna_length": 1734,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1175C>G",
"hgvs_p": "p.Thr392Ser",
"transcript": "XM_047435439.1",
"protein_id": "XP_047291395.1",
"transcript_support_level": null,
"aa_start": 392,
"aa_end": null,
"aa_length": 538,
"cds_start": 1175,
"cds_end": null,
"cds_length": 1617,
"cdna_start": 1296,
"cdna_end": null,
"cdna_length": 1738,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.1175C>G",
"hgvs_p": "p.Thr392Ser",
"transcript": "XM_017024227.2",
"protein_id": "XP_016879716.1",
"transcript_support_level": null,
"aa_start": 392,
"aa_end": null,
"aa_length": 531,
"cds_start": 1175,
"cds_end": null,
"cds_length": 1596,
"cdna_start": 1296,
"cdna_end": null,
"cdna_length": 1966,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.926C>G",
"hgvs_p": "p.Thr309Ser",
"transcript": "XM_047435440.1",
"protein_id": "XP_047291396.1",
"transcript_support_level": null,
"aa_start": 309,
"aa_end": null,
"aa_length": 455,
"cds_start": 926,
"cds_end": null,
"cds_length": 1368,
"cdna_start": 1159,
"cdna_end": null,
"cdna_length": 1601,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "c.641C>G",
"hgvs_p": "p.Thr214Ser",
"transcript": "XM_047435441.1",
"protein_id": "XP_047291397.1",
"transcript_support_level": null,
"aa_start": 214,
"aa_end": null,
"aa_length": 360,
"cds_start": 641,
"cds_end": null,
"cds_length": 1083,
"cdna_start": 725,
"cdna_end": null,
"cdna_length": 1167,
"mane_select": null,
"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": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "n.*1503C>G",
"hgvs_p": null,
"transcript": "ENST00000576630.5",
"protein_id": "ENSP00000458343.2",
"transcript_support_level": 2,
"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": 2266,
"mane_select": null,
"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": 2,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "n.190C>G",
"hgvs_p": null,
"transcript": "ENST00000576714.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 455,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"hgvs_c": "n.*1503C>G",
"hgvs_p": null,
"transcript": "ENST00000576630.5",
"protein_id": "ENSP00000458343.2",
"transcript_support_level": 2,
"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": 2266,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CFAP52",
"gene_hgnc_id": 16053,
"dbsnp": "rs142289033",
"frequency_reference_population": 6.840507e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84051e-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": 0.12927526235580444,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.03999999910593033,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.1,
"revel_prediction": "Benign",
"alphamissense_score": 0.0967,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.55,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.799,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.04,
"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_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000352665.10",
"gene_symbol": "CFAP52",
"hgnc_id": 16053,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.1442C>G",
"hgvs_p": "p.Thr481Ser"
}
],
"clinvar_disease": "Situs inversus",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Situs inversus",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}