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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: 1-150804062-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=150804062&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 150804062,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000271651.8",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "NM_000396.4",
"protein_id": "NP_000387.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 329,
"cds_start": 577,
"cds_end": null,
"cds_length": 990,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1629,
"mane_select": "ENST00000271651.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000271651.8",
"protein_id": "ENSP00000271651.3",
"transcript_support_level": 1,
"aa_start": 193,
"aa_end": null,
"aa_length": 329,
"cds_start": 577,
"cds_end": null,
"cds_length": 990,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1629,
"mane_select": "NM_000396.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.754C>G",
"hgvs_p": "p.Arg252Gly",
"transcript": "ENST00000443913.2",
"protein_id": "ENSP00000405083.2",
"transcript_support_level": 3,
"aa_start": 252,
"aa_end": null,
"aa_length": 388,
"cds_start": 754,
"cds_end": null,
"cds_length": 1167,
"cdna_start": 764,
"cdna_end": null,
"cdna_length": 1768,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.619C>G",
"hgvs_p": "p.Arg207Gly",
"transcript": "ENST00000677887.1",
"protein_id": "ENSP00000503876.1",
"transcript_support_level": null,
"aa_start": 207,
"aa_end": null,
"aa_length": 343,
"cds_start": 619,
"cds_end": null,
"cds_length": 1032,
"cdna_start": 718,
"cdna_end": null,
"cdna_length": 1722,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.613C>G",
"hgvs_p": "p.Arg205Gly",
"transcript": "ENST00000678337.1",
"protein_id": "ENSP00000504759.1",
"transcript_support_level": null,
"aa_start": 205,
"aa_end": null,
"aa_length": 341,
"cds_start": 613,
"cds_end": null,
"cds_length": 1026,
"cdna_start": 1333,
"cdna_end": null,
"cdna_length": 3665,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000676970.1",
"protein_id": "ENSP00000503832.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 333,
"cds_start": 577,
"cds_end": null,
"cds_length": 1002,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1641,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000676751.1",
"protein_id": "ENSP00000502964.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 330,
"cds_start": 577,
"cds_end": null,
"cds_length": 993,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1523,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000676824.1",
"protein_id": "ENSP00000504176.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 329,
"cds_start": 577,
"cds_end": null,
"cds_length": 990,
"cdna_start": 891,
"cdna_end": null,
"cdna_length": 1895,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly",
"transcript": "ENST00000676966.1",
"protein_id": "ENSP00000503723.1",
"transcript_support_level": null,
"aa_start": 193,
"aa_end": null,
"aa_length": 329,
"cds_start": 577,
"cds_end": null,
"cds_length": 990,
"cdna_start": 716,
"cdna_end": null,
"cdna_length": 1720,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.454C>G",
"hgvs_p": "p.Arg152Gly",
"transcript": "ENST00000676716.1",
"protein_id": "ENSP00000504737.1",
"transcript_support_level": null,
"aa_start": 152,
"aa_end": null,
"aa_length": 288,
"cds_start": 454,
"cds_end": null,
"cds_length": 867,
"cdna_start": 455,
"cdna_end": null,
"cdna_length": 1459,
"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": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.3646C>G",
"hgvs_p": null,
"transcript": "ENST00000480670.2",
"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": 4619,
"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": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.577C>G",
"hgvs_p": null,
"transcript": "ENST00000676680.1",
"protein_id": "ENSP00000503270.1",
"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": 1625,
"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": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.2403C>G",
"hgvs_p": null,
"transcript": "ENST00000677330.1",
"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": 3358,
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.429C>G",
"hgvs_p": null,
"transcript": "ENST00000677611.1",
"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": 1427,
"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": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.*469C>G",
"hgvs_p": null,
"transcript": "ENST00000678275.1",
"protein_id": "ENSP00000504796.1",
"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": 1712,
"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": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.1554C>G",
"hgvs_p": null,
"transcript": "ENST00000678725.1",
"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": 2808,
"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": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.1162C>G",
"hgvs_p": null,
"transcript": "ENST00000679090.1",
"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": 2398,
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.3539C>G",
"hgvs_p": null,
"transcript": "ENST00000679148.1",
"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": 4522,
"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": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.2938C>G",
"hgvs_p": null,
"transcript": "ENST00000679171.1",
"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": 4001,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "n.*469C>G",
"hgvs_p": null,
"transcript": "ENST00000678275.1",
"protein_id": "ENSP00000504796.1",
"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": 1712,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 7,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"hgvs_c": "c.399+1799C>G",
"hgvs_p": null,
"transcript": "ENST00000679260.1",
"protein_id": "ENSP00000504534.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 256,
"cds_start": -4,
"cds_end": null,
"cds_length": 771,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1410,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CTSK",
"gene_hgnc_id": 2536,
"dbsnp": "rs747914097",
"frequency_reference_population": 0.0000013680957,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.0000013681,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.09956401586532593,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.366,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0884,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.12,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.092,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM1,PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 2,
"pathogenic_score": 4,
"criteria": [
"PM1",
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000271651.8",
"gene_symbol": "CTSK",
"hgnc_id": 2536,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.577C>G",
"hgvs_p": "p.Arg193Gly"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}