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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: 15-74839331-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=74839331&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 74839331,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001411082.1",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "NM_001099436.4",
"protein_id": "NP_001092906.3",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 472,
"cds_start": 895,
"cds_end": null,
"cds_length": 1419,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000440863.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001099436.4"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000440863.7",
"protein_id": "ENSP00000400312.2",
"transcript_support_level": 2,
"aa_start": 299,
"aa_end": null,
"aa_length": 472,
"cds_start": 895,
"cds_end": null,
"cds_length": 1419,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001099436.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000440863.7"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000569437.5",
"protein_id": "ENSP00000456051.1",
"transcript_support_level": 1,
"aa_start": 299,
"aa_end": null,
"aa_length": 470,
"cds_start": 895,
"cds_end": null,
"cds_length": 1413,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000569437.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "n.1100G>T",
"hgvs_p": null,
"transcript": "ENST00000566479.5",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000566479.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "n.1317G>T",
"hgvs_p": null,
"transcript": "ENST00000570276.5",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000570276.5"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.928G>T",
"hgvs_p": "p.Asp310Tyr",
"transcript": "NM_001411082.1",
"protein_id": "NP_001398011.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 483,
"cds_start": 928,
"cds_end": null,
"cds_length": 1452,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001411082.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.928G>T",
"hgvs_p": "p.Asp310Tyr",
"transcript": "ENST00000568667.5",
"protein_id": "ENSP00000457853.1",
"transcript_support_level": 5,
"aa_start": 310,
"aa_end": null,
"aa_length": 483,
"cds_start": 928,
"cds_end": null,
"cds_length": 1452,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000568667.5"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000894355.1",
"protein_id": "ENSP00000564414.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 478,
"cds_start": 895,
"cds_end": null,
"cds_length": 1437,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894355.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000894356.1",
"protein_id": "ENSP00000564415.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 478,
"cds_start": 895,
"cds_end": null,
"cds_length": 1437,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894356.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000967230.1",
"protein_id": "ENSP00000637289.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 478,
"cds_start": 895,
"cds_end": null,
"cds_length": 1437,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967230.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.892G>T",
"hgvs_p": "p.Asp298Tyr",
"transcript": "ENST00000894360.1",
"protein_id": "ENSP00000564419.1",
"transcript_support_level": null,
"aa_start": 298,
"aa_end": null,
"aa_length": 477,
"cds_start": 892,
"cds_end": null,
"cds_length": 1434,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894360.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000894358.1",
"protein_id": "ENSP00000564417.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 476,
"cds_start": 895,
"cds_end": null,
"cds_length": 1431,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894358.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000967232.1",
"protein_id": "ENSP00000637291.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 476,
"cds_start": 895,
"cds_end": null,
"cds_length": 1431,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967232.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.892G>T",
"hgvs_p": "p.Asp298Tyr",
"transcript": "ENST00000894350.1",
"protein_id": "ENSP00000564409.1",
"transcript_support_level": null,
"aa_start": 298,
"aa_end": null,
"aa_length": 471,
"cds_start": 892,
"cds_end": null,
"cds_length": 1416,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894350.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.892G>T",
"hgvs_p": "p.Asp298Tyr",
"transcript": "ENST00000894351.1",
"protein_id": "ENSP00000564410.1",
"transcript_support_level": null,
"aa_start": 298,
"aa_end": null,
"aa_length": 471,
"cds_start": 892,
"cds_end": null,
"cds_length": 1416,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894351.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000926382.1",
"protein_id": "ENSP00000596441.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 471,
"cds_start": 895,
"cds_end": null,
"cds_length": 1416,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926382.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "NM_001284364.3",
"protein_id": "NP_001271293.2",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 470,
"cds_start": 895,
"cds_end": null,
"cds_length": 1413,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284364.3"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000926383.1",
"protein_id": "ENSP00000596442.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 470,
"cds_start": 895,
"cds_end": null,
"cds_length": 1413,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000926383.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.892G>T",
"hgvs_p": "p.Asp298Tyr",
"transcript": "ENST00000894348.1",
"protein_id": "ENSP00000564407.1",
"transcript_support_level": null,
"aa_start": 298,
"aa_end": null,
"aa_length": 469,
"cds_start": 892,
"cds_end": null,
"cds_length": 1410,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894348.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.892G>T",
"hgvs_p": "p.Asp298Tyr",
"transcript": "ENST00000894353.1",
"protein_id": "ENSP00000564412.1",
"transcript_support_level": null,
"aa_start": 298,
"aa_end": null,
"aa_length": 469,
"cds_start": 892,
"cds_end": null,
"cds_length": 1410,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000894353.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000967231.1",
"protein_id": "ENSP00000637290.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 469,
"cds_start": 895,
"cds_end": null,
"cds_length": 1410,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000967231.1"
},
{
"aa_ref": "D",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ULK3",
"gene_hgnc_id": 19703,
"hgvs_c": "c.895G>T",
"hgvs_p": "p.Asp299Tyr",
"transcript": "ENST00000894354.1",
"protein_id": "ENSP00000564413.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 468,
"cds_start": 895,
"cds_end": null,
"cds_length": 1407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
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"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
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"revel_prediction": "Benign",
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"bayesdelnoaf_score": -0.3,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.843,
"phylop100way_prediction": "Uncertain_significance",
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"acmg_score": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "NM_001411082.1",
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"effects": [
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"inheritance_mode": "AR",
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],
"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
}