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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: 11-74457349-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=74457349&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 74457349,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000310128.9",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "NM_005472.5",
"protein_id": "NP_005463.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 556,
"cdna_end": null,
"cdna_length": 3064,
"mane_select": "ENST00000310128.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "ENST00000310128.9",
"protein_id": "ENSP00000310557.4",
"transcript_support_level": 1,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 556,
"cdna_end": null,
"cdna_length": 3064,
"mane_select": "NM_005472.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "ENST00000525550.1",
"protein_id": "ENSP00000433633.1",
"transcript_support_level": 1,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 668,
"cdna_end": null,
"cdna_length": 935,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "ENST00000532569.5",
"protein_id": "ENSP00000431739.1",
"transcript_support_level": 4,
"aa_start": 72,
"aa_end": null,
"aa_length": 98,
"cds_start": 215,
"cds_end": null,
"cds_length": 298,
"cdna_start": 502,
"cdna_end": null,
"cdna_length": 585,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.347T>C",
"hgvs_p": "p.Val116Ala",
"transcript": "XM_011544713.3",
"protein_id": "XP_011543015.1",
"transcript_support_level": null,
"aa_start": 116,
"aa_end": null,
"aa_length": 147,
"cds_start": 347,
"cds_end": null,
"cds_length": 444,
"cdna_start": 407,
"cdna_end": null,
"cdna_length": 2915,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_017017047.2",
"protein_id": "XP_016872536.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 664,
"cdna_end": null,
"cdna_length": 3172,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_017017048.2",
"protein_id": "XP_016872537.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 728,
"cdna_end": null,
"cdna_length": 3236,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_017017049.2",
"protein_id": "XP_016872538.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 3086,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_017017051.3",
"protein_id": "XP_016872540.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 620,
"cdna_end": null,
"cdna_length": 3128,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_047426176.1",
"protein_id": "XP_047282132.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 433,
"cdna_end": null,
"cdna_length": 2941,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala",
"transcript": "XM_047426177.1",
"protein_id": "XP_047282133.1",
"transcript_support_level": null,
"aa_start": 72,
"aa_end": null,
"aa_length": 103,
"cds_start": 215,
"cds_end": null,
"cds_length": 312,
"cdna_start": 3464,
"cdna_end": null,
"cdna_length": 5972,
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000254928",
"gene_hgnc_id": null,
"hgvs_c": "n.830A>G",
"hgvs_p": null,
"transcript": "ENST00000759310.1",
"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": 1329,
"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": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ENSG00000254631",
"gene_hgnc_id": null,
"hgvs_c": "n.155-26828A>G",
"hgvs_p": null,
"transcript": "ENST00000533008.1",
"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": 344,
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.*57T>C",
"hgvs_p": null,
"transcript": "ENST00000531854.5",
"protein_id": "ENSP00000433697.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 51,
"cds_start": -4,
"cds_end": null,
"cds_length": 158,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 607,
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.*66T>C",
"hgvs_p": null,
"transcript": "ENST00000529425.5",
"protein_id": "ENSP00000434890.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 48,
"cds_start": -4,
"cds_end": null,
"cds_length": 149,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 555,
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"hgvs_c": "c.*178T>C",
"hgvs_p": null,
"transcript": "ENST00000526855.1",
"protein_id": "ENSP00000435539.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 11,
"cds_start": -4,
"cds_end": null,
"cds_length": 37,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 550,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "KCNE3",
"gene_hgnc_id": 6243,
"dbsnp": "rs202036216",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5619441270828247,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.566,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.4707,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.21,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 6.11,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000310128.9",
"gene_symbol": "KCNE3",
"hgnc_id": 6243,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.215T>C",
"hgvs_p": "p.Val72Ala"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000759310.1",
"gene_symbol": "ENSG00000254928",
"hgnc_id": null,
"effects": [
"non_coding_transcript_exon_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.830A>G",
"hgvs_p": null
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000533008.1",
"gene_symbol": "ENSG00000254631",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.155-26828A>G",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}