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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: 20-45025072-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=45025072&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "20",
"pos": 45025072,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000372806.8",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1247C>T",
"hgvs_p": "p.Pro416Leu",
"transcript": "NM_006282.5",
"protein_id": "NP_006273.1",
"transcript_support_level": null,
"aa_start": 416,
"aa_end": null,
"aa_length": 487,
"cds_start": 1247,
"cds_end": null,
"cds_length": 1464,
"cdna_start": 1304,
"cdna_end": null,
"cdna_length": 6366,
"mane_select": "ENST00000372806.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1247C>T",
"hgvs_p": "p.Pro416Leu",
"transcript": "ENST00000372806.8",
"protein_id": "ENSP00000361892.3",
"transcript_support_level": 1,
"aa_start": 416,
"aa_end": null,
"aa_length": 487,
"cds_start": 1247,
"cds_end": null,
"cds_length": 1464,
"cdna_start": 1304,
"cdna_end": null,
"cdna_length": 6366,
"mane_select": "NM_006282.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1082C>T",
"hgvs_p": "p.Pro361Leu",
"transcript": "ENST00000499879.8",
"protein_id": "ENSP00000443514.1",
"transcript_support_level": 1,
"aa_start": 361,
"aa_end": null,
"aa_length": 432,
"cds_start": 1082,
"cds_end": null,
"cds_length": 1299,
"cdna_start": 1125,
"cdna_end": null,
"cdna_length": 10380,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"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": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1247C>T",
"hgvs_p": "p.Pro416Leu",
"transcript": "NM_001352385.2",
"protein_id": "NP_001339314.1",
"transcript_support_level": null,
"aa_start": 416,
"aa_end": null,
"aa_length": 462,
"cds_start": 1247,
"cds_end": null,
"cds_length": 1389,
"cdna_start": 1304,
"cdna_end": null,
"cdna_length": 6461,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"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": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1247C>T",
"hgvs_p": "p.Pro416Leu",
"transcript": "ENST00000372801.5",
"protein_id": "ENSP00000361887.1",
"transcript_support_level": 2,
"aa_start": 416,
"aa_end": null,
"aa_length": 462,
"cds_start": 1247,
"cds_end": null,
"cds_length": 1389,
"cdna_start": 1294,
"cdna_end": null,
"cdna_length": 2038,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1019C>T",
"hgvs_p": "p.Pro340Leu",
"transcript": "ENST00000474717.3",
"protein_id": "ENSP00000479564.2",
"transcript_support_level": 3,
"aa_start": 340,
"aa_end": null,
"aa_length": 411,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 1276,
"cdna_end": null,
"cdna_length": 6286,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1208C>T",
"hgvs_p": "p.Pro403Leu",
"transcript": "XM_005260532.5",
"protein_id": "XP_005260589.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 474,
"cds_start": 1208,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 5393,
"cdna_end": null,
"cdna_length": 10455,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1208C>T",
"hgvs_p": "p.Pro403Leu",
"transcript": "XM_017028031.3",
"protein_id": "XP_016883520.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 474,
"cds_start": 1208,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 6768,
"cdna_end": null,
"cdna_length": 11830,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1208C>T",
"hgvs_p": "p.Pro403Leu",
"transcript": "XM_047440425.1",
"protein_id": "XP_047296381.1",
"transcript_support_level": null,
"aa_start": 403,
"aa_end": null,
"aa_length": 474,
"cds_start": 1208,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 6750,
"cdna_end": null,
"cdna_length": 11812,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1160C>T",
"hgvs_p": "p.Pro387Leu",
"transcript": "XM_047440426.1",
"protein_id": "XP_047296382.1",
"transcript_support_level": null,
"aa_start": 387,
"aa_end": null,
"aa_length": 458,
"cds_start": 1160,
"cds_end": null,
"cds_length": 1377,
"cdna_start": 1249,
"cdna_end": null,
"cdna_length": 6311,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.1019C>T",
"hgvs_p": "p.Pro340Leu",
"transcript": "XM_011529018.4",
"protein_id": "XP_011527320.1",
"transcript_support_level": null,
"aa_start": 340,
"aa_end": null,
"aa_length": 411,
"cds_start": 1019,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 5457,
"cdna_end": null,
"cdna_length": 10519,
"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": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "n.*299C>T",
"hgvs_p": null,
"transcript": "ENST00000698221.1",
"protein_id": "ENSP00000513614.1",
"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": 2115,
"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": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "n.*1208C>T",
"hgvs_p": null,
"transcript": "ENST00000698222.1",
"protein_id": "ENSP00000513615.1",
"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": 2010,
"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": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "n.1622C>T",
"hgvs_p": null,
"transcript": "ENST00000698225.1",
"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": 2260,
"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": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "n.*299C>T",
"hgvs_p": null,
"transcript": "ENST00000698221.1",
"protein_id": "ENSP00000513614.1",
"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": 2115,
"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": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "n.*1208C>T",
"hgvs_p": null,
"transcript": "ENST00000698222.1",
"protein_id": "ENSP00000513615.1",
"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": 2010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"hgvs_c": "c.*141C>T",
"hgvs_p": null,
"transcript": "XM_017028033.2",
"protein_id": "XP_016883522.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 388,
"cds_start": -4,
"cds_end": null,
"cds_length": 1167,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1324,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "STK4",
"gene_hgnc_id": 11408,
"dbsnp": "rs33963346",
"frequency_reference_population": 0.01107989,
"hom_count_reference_population": 120,
"allele_count_reference_population": 17870,
"gnomad_exomes_af": 0.0114971,
"gnomad_genomes_af": 0.00707879,
"gnomad_exomes_ac": 16792,
"gnomad_genomes_ac": 1078,
"gnomad_exomes_homalt": 114,
"gnomad_genomes_homalt": 6,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.0074424147605896,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.291,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0762,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.32,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.83,
"phylop100way_prediction": "Uncertain_significance",
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000372806.8",
"gene_symbol": "STK4",
"hgnc_id": 11408,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1247C>T",
"hgvs_p": "p.Pro416Leu"
}
],
"clinvar_disease": "Combined immunodeficiency due to STK4 deficiency,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:3",
"phenotype_combined": "Combined immunodeficiency due to STK4 deficiency|not specified|not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}