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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: 2-169509975-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=169509975&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 169509975,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_006063.3",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "NM_006063.3",
"protein_id": "NP_006054.2",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 606,
"cds_start": 197,
"cds_end": null,
"cds_length": 1821,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000284669.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006063.3"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "ENST00000284669.2",
"protein_id": "ENSP00000284669.1",
"transcript_support_level": 1,
"aa_start": 66,
"aa_end": null,
"aa_length": 606,
"cds_start": 197,
"cds_end": null,
"cds_length": 1821,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_006063.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000284669.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ENSG00000251569",
"gene_hgnc_id": null,
"hgvs_c": "c.925-4599T>C",
"hgvs_p": null,
"transcript": "ENST00000513963.1",
"protein_id": "ENSP00000424363.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 544,
"cds_start": null,
"cds_end": null,
"cds_length": 1635,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000513963.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "ENST00000946624.1",
"protein_id": "ENSP00000616683.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 617,
"cds_start": 197,
"cds_end": null,
"cds_length": 1854,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946624.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "ENST00000946625.1",
"protein_id": "ENSP00000616684.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 557,
"cds_start": 197,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946625.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "ENST00000946627.1",
"protein_id": "ENSP00000616686.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 544,
"cds_start": 197,
"cds_end": null,
"cds_length": 1635,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946627.1"
},
{
"aa_ref": "I",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr",
"transcript": "ENST00000946626.1",
"protein_id": "ENSP00000616685.1",
"transcript_support_level": null,
"aa_start": 66,
"aa_end": null,
"aa_length": 495,
"cds_start": 197,
"cds_end": null,
"cds_length": 1488,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946626.1"
}
],
"gene_symbol": "KLHL41",
"gene_hgnc_id": 16905,
"dbsnp": "rs116809051",
"frequency_reference_population": 0.00048385738,
"hom_count_reference_population": 1,
"allele_count_reference_population": 781,
"gnomad_exomes_af": 0.000394702,
"gnomad_genomes_af": 0.0013399,
"gnomad_exomes_ac": 577,
"gnomad_genomes_ac": 204,
"gnomad_exomes_homalt": 1,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.003551870584487915,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.115,
"revel_prediction": "Benign",
"alphamissense_score": 0.0542,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.33,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 6.489,
"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": -16,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1",
"acmg_by_gene": [
{
"score": -16,
"benign_score": 16,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1"
],
"verdict": "Benign",
"transcript": "NM_006063.3",
"gene_symbol": "KLHL41",
"hgnc_id": 16905,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.197T>C",
"hgvs_p": "p.Ile66Thr"
},
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong"
],
"verdict": "Benign",
"transcript": "ENST00000513963.1",
"gene_symbol": "ENSG00000251569",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.925-4599T>C",
"hgvs_p": null
}
],
"clinvar_disease": "KLHL41-related disorder,Nemaline myopathy 9,not provided",
"clinvar_classification": "Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:2",
"phenotype_combined": "not provided|Nemaline myopathy 9|KLHL41-related disorder",
"pathogenicity_classification_combined": "Likely benign",
"custom_annotations": null
}
],
"message": null
}