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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: 1-215124745-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=215124745&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 215124745,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000444842.7",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.470C>G",
"hgvs_p": "p.Thr157Ser",
"transcript": "NM_001017425.3",
"protein_id": "NP_001017425.2",
"transcript_support_level": null,
"aa_start": 157,
"aa_end": null,
"aa_length": 426,
"cds_start": 470,
"cds_end": null,
"cds_length": 1281,
"cdna_start": 1119,
"cdna_end": null,
"cdna_length": 3875,
"mane_select": "ENST00000444842.7",
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.470C>G",
"hgvs_p": "p.Thr157Ser",
"transcript": "ENST00000444842.7",
"protein_id": "ENSP00000394033.2",
"transcript_support_level": 1,
"aa_start": 157,
"aa_end": null,
"aa_length": 426,
"cds_start": 470,
"cds_end": null,
"cds_length": 1281,
"cdna_start": 1119,
"cdna_end": null,
"cdna_length": 3875,
"mane_select": "NM_001017425.3",
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.458C>G",
"hgvs_p": "p.Thr153Ser",
"transcript": "ENST00000391895.6",
"protein_id": "ENSP00000375765.2",
"transcript_support_level": 1,
"aa_start": 153,
"aa_end": null,
"aa_length": 422,
"cds_start": 458,
"cds_end": null,
"cds_length": 1269,
"cdna_start": 525,
"cdna_end": null,
"cdna_length": 1410,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.425C>G",
"hgvs_p": "p.Thr142Ser",
"transcript": "ENST00000391894.6",
"protein_id": "ENSP00000375764.2",
"transcript_support_level": 1,
"aa_start": 142,
"aa_end": null,
"aa_length": 411,
"cds_start": 425,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 608,
"cdna_end": null,
"cdna_length": 1491,
"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": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "n.458C>G",
"hgvs_p": null,
"transcript": "ENST00000467031.5",
"protein_id": "ENSP00000420203.1",
"transcript_support_level": 1,
"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": 1200,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.458C>G",
"hgvs_p": "p.Thr153Ser",
"transcript": "NM_001017424.3",
"protein_id": "NP_001017424.1",
"transcript_support_level": null,
"aa_start": 153,
"aa_end": null,
"aa_length": 422,
"cds_start": 458,
"cds_end": null,
"cds_length": 1269,
"cdna_start": 838,
"cdna_end": null,
"cdna_length": 3594,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.425C>G",
"hgvs_p": "p.Thr142Ser",
"transcript": "NM_014217.4",
"protein_id": "NP_055032.1",
"transcript_support_level": null,
"aa_start": 142,
"aa_end": null,
"aa_length": 411,
"cds_start": 425,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 995,
"cdna_end": null,
"cdna_length": 3751,
"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": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.302C>G",
"hgvs_p": "p.Thr101Ser",
"transcript": "ENST00000457122.1",
"protein_id": "ENSP00000413460.1",
"transcript_support_level": 3,
"aa_start": 101,
"aa_end": null,
"aa_length": 123,
"cds_start": 302,
"cds_end": null,
"cds_length": 374,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 644,
"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": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.302C>G",
"hgvs_p": "p.Thr101Ser",
"transcript": "ENST00000478774.5",
"protein_id": "ENSP00000420569.1",
"transcript_support_level": 4,
"aa_start": 101,
"aa_end": null,
"aa_length": 117,
"cds_start": 302,
"cds_end": null,
"cds_length": 354,
"cdna_start": 514,
"cdna_end": null,
"cdna_length": 566,
"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": 4,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.428C>G",
"hgvs_p": "p.Thr143Ser",
"transcript": "XM_017001249.2",
"protein_id": "XP_016856738.1",
"transcript_support_level": null,
"aa_start": 143,
"aa_end": null,
"aa_length": 412,
"cds_start": 428,
"cds_end": null,
"cds_length": 1239,
"cdna_start": 926,
"cdna_end": null,
"cdna_length": 3682,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.302C>G",
"hgvs_p": "p.Thr101Ser",
"transcript": "XM_011509522.3",
"protein_id": "XP_011507824.1",
"transcript_support_level": null,
"aa_start": 101,
"aa_end": null,
"aa_length": 370,
"cds_start": 302,
"cds_end": null,
"cds_length": 1113,
"cdna_start": 485,
"cdna_end": null,
"cdna_length": 3241,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.302C>G",
"hgvs_p": "p.Thr101Ser",
"transcript": "XM_011509524.3",
"protein_id": "XP_011507826.1",
"transcript_support_level": null,
"aa_start": 101,
"aa_end": null,
"aa_length": 370,
"cds_start": 302,
"cds_end": null,
"cds_length": 1113,
"cdna_start": 766,
"cdna_end": null,
"cdna_length": 3522,
"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": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "c.302C>G",
"hgvs_p": "p.Thr101Ser",
"transcript": "XM_047419881.1",
"protein_id": "XP_047275837.1",
"transcript_support_level": null,
"aa_start": 101,
"aa_end": null,
"aa_length": 370,
"cds_start": 302,
"cds_end": null,
"cds_length": 1113,
"cdna_start": 528,
"cdna_end": null,
"cdna_length": 3284,
"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": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "n.425C>G",
"hgvs_p": null,
"transcript": "ENST00000474771.5",
"protein_id": "ENSP00000420499.1",
"transcript_support_level": 5,
"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": 1130,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "n.357+38067C>G",
"hgvs_p": null,
"transcript": "ENST00000470177.5",
"protein_id": "ENSP00000419633.1",
"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": 961,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"hgvs_c": "n.345+38067C>G",
"hgvs_p": null,
"transcript": "ENST00000486921.5",
"protein_id": "ENSP00000418706.1",
"transcript_support_level": 5,
"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": 1662,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "KCNK2",
"gene_hgnc_id": 6277,
"dbsnp": "rs1408770204",
"frequency_reference_population": 0.0000012791747,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 7.08525e-7,
"gnomad_genomes_af": 0.0000065735,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8770415782928467,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05999999865889549,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.63,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.9857,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.25,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.337,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.06,
"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": 4,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3_Moderate",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000444842.7",
"gene_symbol": "KCNK2",
"hgnc_id": 6277,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.470C>G",
"hgvs_p": "p.Thr157Ser"
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}