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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: 12-16352362-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=16352362&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 16352362,
"ref": "G",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000396210.8",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_020300.5",
"protein_id": "NP_064696.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": -4,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 925,
"mane_select": "ENST00000396210.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "ENST00000396210.8",
"protein_id": "ENSP00000379513.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": -4,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 925,
"mane_select": "NM_020300.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "ENST00000535309.5",
"protein_id": "ENSP00000438308.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 87,
"cds_start": -4,
"cds_end": null,
"cds_length": 264,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1331,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "n.57+4652G>A",
"hgvs_p": null,
"transcript": "ENST00000542256.5",
"protein_id": null,
"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": 933,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_001414355.1",
"protein_id": "NP_001401284.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 160,
"cds_start": -4,
"cds_end": null,
"cds_length": 483,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 940,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_001414356.1",
"protein_id": "NP_001401285.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 157,
"cds_start": -4,
"cds_end": null,
"cds_length": 474,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 931,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-15-1876G>A",
"hgvs_p": null,
"transcript": "NM_001260511.2",
"protein_id": "NP_001247440.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": -4,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 918,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_001414357.1",
"protein_id": "NP_001401286.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": -4,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1022,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-15-1876G>A",
"hgvs_p": null,
"transcript": "NM_001414358.1",
"protein_id": "NP_001401287.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": -4,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 922,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
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"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_001414359.1",
"protein_id": "NP_001401288.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 155,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "NM_145791.3",
"protein_id": "NP_665734.1",
"transcript_support_level": null,
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},
{
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"strand": true,
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],
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-22-1869G>A",
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"transcript": "NM_145792.3",
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},
{
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],
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-22-1869G>A",
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"transcript": "ENST00000010404.6",
"protein_id": "ENSP00000010404.2",
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"aa_start": null,
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{
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],
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"hgvs_c": "c.-22-1869G>A",
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],
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},
{
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],
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-3-1909G>A",
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"transcript": "NM_001414361.1",
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],
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},
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],
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"intron_rank": 1,
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-22-1869G>A",
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"transcript": "NM_001414363.1",
"protein_id": "NP_001401292.1",
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},
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"strand": true,
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],
"exon_rank": null,
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"intron_rank": 1,
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-22-1869G>A",
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],
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],
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},
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],
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"gene_symbol": "MGST1",
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"hgvs_c": "c.-22-1869G>A",
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"transcript": "NM_001260512.2",
"protein_id": "NP_001247441.1",
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"biotype": null,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "MGST1",
"gene_hgnc_id": 7061,
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null,
"transcript": "ENST00000543076.5",
"protein_id": "ENSP00000442767.1",
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},
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"gnomad_genomes_ac": 106554,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": 37658,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.9100000262260437,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.91,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.341,
"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": -12,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BA1",
"acmg_by_gene": [
{
"score": -12,
"benign_score": 12,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000396210.8",
"gene_symbol": "MGST1",
"hgnc_id": 7061,
"effects": [
"intron_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.-22-1869G>A",
"hgvs_p": null
}
],
"clinvar_disease": " chronic obstructive, susceptibility to,Pulmonary disease",
"clinvar_classification": "association",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Pulmonary disease, chronic obstructive, susceptibility to",
"pathogenicity_classification_combined": "association",
"custom_annotations": null
}
],
"message": null
}