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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: 7-66089146-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=66089146&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [
"PM1",
"PM2",
"PM5",
"PP2",
"PP3_Strong",
"PP5"
],
"effects": [
"missense_variant"
],
"gene_symbol": "ASL",
"hgnc_id": 746,
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"inheritance_mode": "AR",
"pathogenic_score": 12,
"score": 12,
"transcript": "NM_000048.4",
"verdict": "Pathogenic"
},
{
"benign_score": 0,
"criteria": [
"PM1",
"PM2",
"PM5",
"PP3_Strong",
"PP5"
],
"effects": [
"missense_variant"
],
"gene_symbol": "ENSG00000249319",
"hgnc_id": null,
"hgvs_c": "c.202C>T",
"hgvs_p": "p.Arg68Trp",
"inheritance_mode": "",
"pathogenic_score": 11,
"score": 11,
"transcript": "ENST00000450043.2",
"verdict": "Pathogenic"
}
],
"acmg_classification": "Pathogenic",
"acmg_criteria": "PM1,PM2,PM5,PP2,PP3_Strong,PP5",
"acmg_score": 12,
"allele_count_reference_population": 4,
"alphamissense_prediction": null,
"alphamissense_score": 0.9226,
"alt": "T",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.57,
"chr": "7",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_disease": "Argininosuccinate lyase deficiency,not specified",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "P:1 LP:1 US:1",
"computational_prediction_selected": "Pathogenic",
"computational_score_selected": 0.9924460053443909,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 464,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2140,
"cdna_start": 970,
"cds_end": null,
"cds_length": 1395,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_000048.4",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000304874.14",
"protein_coding": true,
"protein_id": "NP_000039.2",
"strand": true,
"transcript": "NM_000048.4",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 464,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 2140,
"cdna_start": 970,
"cds_end": null,
"cds_length": 1395,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000304874.14",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_000048.4",
"protein_coding": true,
"protein_id": "ENSP00000307188.9",
"strand": true,
"transcript": "ENST00000304874.14",
"transcript_support_level": 1
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 464,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1608,
"cdna_start": 1082,
"cds_end": null,
"cds_length": 1395,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000395332.8",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000378741.3",
"strand": true,
"transcript": "ENST00000395332.8",
"transcript_support_level": 1
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 306,
"aa_ref": "R",
"aa_start": 68,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 922,
"cdna_start": 202,
"cds_end": null,
"cds_length": 922,
"cds_start": 202,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000450043.2",
"gene_hgnc_id": null,
"gene_symbol": "ENSG00000249319",
"hgvs_c": "c.202C>T",
"hgvs_p": "p.Arg68Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000396527.2",
"strand": true,
"transcript": "ENST00000450043.2",
"transcript_support_level": 5
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 495,
"aa_ref": "R",
"aa_start": 328,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1612,
"cdna_start": 1063,
"cds_end": null,
"cds_length": 1488,
"cds_start": 982,
"consequences": [
"missense_variant"
],
"exon_count": 18,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000906815.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.982C>T",
"hgvs_p": "p.Arg328Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576874.1",
"strand": true,
"transcript": "ENST00000906815.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 474,
"aa_ref": "R",
"aa_start": 307,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1532,
"cdna_start": 985,
"cds_end": null,
"cds_length": 1425,
"cds_start": 919,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906826.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.919C>T",
"hgvs_p": "p.Arg307Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576885.1",
"strand": true,
"transcript": "ENST00000906826.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 474,
"aa_ref": "R",
"aa_start": 307,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1688,
"cdna_start": 1142,
"cds_end": null,
"cds_length": 1425,
"cds_start": 919,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000906828.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.919C>T",
"hgvs_p": "p.Arg307Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576887.1",
"strand": true,
"transcript": "ENST00000906828.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 473,
"aa_ref": "R",
"aa_start": 306,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1605,
"cdna_start": 1058,
"cds_end": null,
"cds_length": 1422,
"cds_start": 916,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000952733.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.916C>T",
"hgvs_p": "p.Arg306Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000622792.1",
"strand": true,
"transcript": "ENST00000952733.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 464,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2322,
"cdna_start": 1152,
"cds_end": null,
"cds_length": 1395,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001024943.2",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020114.1",
"strand": true,
"transcript": "NM_001024943.2",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 464,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2006,
"cdna_start": 1069,
"cds_end": null,
"cds_length": 1395,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906801.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576860.1",
"strand": true,
"transcript": "ENST00000906801.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 463,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1752,
"cdna_start": 970,
"cds_end": null,
"cds_length": 1392,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906807.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576866.1",
"strand": true,
"transcript": "ENST00000906807.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 459,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1497,
"cdna_start": 967,
"cds_end": null,
"cds_length": 1380,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906823.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576882.1",
"strand": true,
"transcript": "ENST00000906823.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 449,
"aa_ref": "R",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1466,
"cdna_start": 925,
"cds_end": null,
"cds_length": 1350,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906824.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.844C>T",
"hgvs_p": "p.Arg282Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576883.1",
"strand": true,
"transcript": "ENST00000906824.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 445,
"aa_ref": "R",
"aa_start": 278,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1558,
"cdna_start": 1011,
"cds_end": null,
"cds_length": 1338,
"cds_start": 832,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000952732.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.832C>T",
"hgvs_p": "p.Arg278Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000622791.1",
"strand": true,
"transcript": "ENST00000952732.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 444,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2262,
"cdna_start": 1152,
"cds_end": null,
"cds_length": 1335,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001024944.2",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020115.1",
"strand": true,
"transcript": "NM_001024944.2",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 444,
"aa_ref": "R",
"aa_start": 297,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1478,
"cdna_start": 1027,
"cds_end": null,
"cds_length": 1335,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000395331.4",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000378740.3",
"strand": true,
"transcript": "ENST00000395331.4",
"transcript_support_level": 5
},
{
"aa_alt": "W",
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"aa_length": 444,
"aa_ref": "R",
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"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1678,
"cdna_start": 970,
"cds_end": null,
"cds_length": 1335,
"cds_start": 889,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000906808.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.889C>T",
"hgvs_p": "p.Arg297Trp",
"intron_rank": null,
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"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000576867.1",
"strand": true,
"transcript": "ENST00000906808.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
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"aa_length": 438,
"aa_ref": "R",
"aa_start": 271,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2244,
"cdna_start": 1074,
"cds_end": null,
"cds_length": 1317,
"cds_start": 811,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "NM_001024946.2",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.811C>T",
"hgvs_p": "p.Arg271Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020117.1",
"strand": true,
"transcript": "NM_001024946.2",
"transcript_support_level": null
},
{
"aa_alt": "W",
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"aa_length": 438,
"aa_ref": "R",
"aa_start": 271,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1974,
"cdna_start": 1046,
"cds_end": null,
"cds_length": 1317,
"cds_start": 811,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000380839.9",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.811C>T",
"hgvs_p": "p.Arg271Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000370219.4",
"strand": true,
"transcript": "ENST00000380839.9",
"transcript_support_level": 5
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 438,
"aa_ref": "R",
"aa_start": 271,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1436,
"cdna_start": 889,
"cds_end": null,
"cds_length": 1317,
"cds_start": 811,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000673518.1",
"gene_hgnc_id": 746,
"gene_symbol": "ASL",
"hgvs_c": "c.811C>T",
"hgvs_p": "p.Arg271Trp",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000499889.1",
"strand": true,
"transcript": "ENST00000673518.1",
"transcript_support_level": null
},
{
"aa_alt": "W",
"aa_end": null,
"aa_length": 438,
"aa_ref": "R",
"aa_start": 271,
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}
],
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}
]
}