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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: 22-28694058-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=28694058&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 2,
"criteria": [
"PM1",
"PM2",
"BP4_Moderate"
],
"effects": [
"missense_variant"
],
"gene_symbol": "CHEK2",
"hgnc_id": 16627,
"hgvs_c": "c.1564G>C",
"hgvs_p": "p.Glu522Gln",
"inheritance_mode": "AD,Unknown",
"pathogenic_score": 4,
"score": 2,
"transcript": "NM_001005735.3",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM1,PM2,BP4_Moderate",
"acmg_score": 2,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": 0.1282,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.42,
"chr": "22",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.15089911222457886,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1844,
"cdna_start": 1493,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_007194.4",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000404276.6",
"protein_coding": true,
"protein_id": "NP_009125.1",
"strand": false,
"transcript": "NM_007194.4",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1844,
"cdna_start": 1493,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000404276.6",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_007194.4",
"protein_coding": true,
"protein_id": "ENSP00000385747.1",
"strand": false,
"transcript": "ENST00000404276.6",
"transcript_support_level": 1
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 586,
"aa_ref": "E",
"aa_start": 522,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1971,
"cdna_start": 1640,
"cds_end": null,
"cds_length": 1761,
"cds_start": 1564,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000382580.6",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1564G>C",
"hgvs_p": "p.Glu522Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000372023.2",
"strand": false,
"transcript": "ENST00000382580.6",
"transcript_support_level": 1
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 476,
"aa_ref": "E",
"aa_start": 412,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1591,
"cdna_start": 1240,
"cds_end": null,
"cds_length": 1431,
"cds_start": 1234,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000402731.6",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1234G>C",
"hgvs_p": "p.Glu412Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000384835.2",
"strand": false,
"transcript": "ENST00000402731.6",
"transcript_support_level": 1
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 452,
"aa_ref": "E",
"aa_start": 388,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1359,
"cdna_start": 1162,
"cds_end": null,
"cds_length": 1359,
"cds_start": 1162,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000403642.5",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1162G>C",
"hgvs_p": "p.Glu388Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000384919.1",
"strand": false,
"transcript": "ENST00000403642.5",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2560,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000416671.5",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "n.*925G>C",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000402225.1",
"strand": false,
"transcript": "ENST00000416671.5",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 2560,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000416671.5",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "n.*925G>C",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000402225.1",
"strand": false,
"transcript": "ENST00000416671.5",
"transcript_support_level": 1
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 586,
"aa_ref": "E",
"aa_start": 522,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1974,
"cdna_start": 1622,
"cds_end": null,
"cds_length": 1761,
"cds_start": 1564,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "NM_001005735.3",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1564G>C",
"hgvs_p": "p.Glu522Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001005735.1",
"strand": false,
"transcript": "NM_001005735.3",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 574,
"aa_ref": "E",
"aa_start": 510,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1938,
"cdna_start": 1586,
"cds_end": null,
"cds_length": 1725,
"cds_start": 1528,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "NM_001438293.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1528G>C",
"hgvs_p": "p.Glu510Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425222.1",
"strand": false,
"transcript": "NM_001438293.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 557,
"aa_ref": "E",
"aa_start": 493,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1887,
"cdna_start": 1535,
"cds_end": null,
"cds_length": 1674,
"cds_start": 1477,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001438294.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1477G>C",
"hgvs_p": "p.Glu493Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425223.1",
"strand": false,
"transcript": "NM_001438294.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 546,
"aa_ref": "E",
"aa_start": 482,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1859,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1641,
"cds_start": 1444,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000928685.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1444G>C",
"hgvs_p": "p.Glu482Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000598744.1",
"strand": false,
"transcript": "ENST00000928685.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 545,
"aa_ref": "E",
"aa_start": 481,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1851,
"cdna_start": 1499,
"cds_end": null,
"cds_length": 1638,
"cds_start": 1441,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001438295.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1441G>C",
"hgvs_p": "p.Glu481Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001425224.1",
"strand": false,
"transcript": "NM_001438295.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1959,
"cdna_start": 1627,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000405598.5",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000386087.1",
"strand": false,
"transcript": "ENST00000405598.5",
"transcript_support_level": 5
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1923,
"cdna_start": 1595,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000650281.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000497000.1",
"strand": false,
"transcript": "ENST00000650281.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2522,
"cdna_start": 2172,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899937.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569996.1",
"strand": false,
"transcript": "ENST00000899937.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2601,
"cdna_start": 2250,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000928690.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000598749.1",
"strand": false,
"transcript": "ENST00000928690.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1886,
"cdna_start": 1536,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000928691.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000598750.1",
"strand": false,
"transcript": "ENST00000928691.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2042,
"cdna_start": 1691,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 15,
"exon_rank_end": null,
"feature": "ENST00000928694.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000598753.1",
"strand": false,
"transcript": "ENST00000928694.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 543,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2011,
"cdna_start": 1661,
"cds_end": null,
"cds_length": 1632,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 14,
"exon_rank_end": null,
"feature": "ENST00000954618.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000624677.1",
"strand": false,
"transcript": "ENST00000954618.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 541,
"aa_ref": "E",
"aa_start": 477,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1874,
"cdna_start": 1518,
"cds_end": null,
"cds_length": 1626,
"cds_start": 1429,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000928683.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1429G>C",
"hgvs_p": "p.Glu477Gln",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000598742.1",
"strand": false,
"transcript": "ENST00000928683.1",
"transcript_support_level": null
},
{
"aa_alt": "Q",
"aa_end": null,
"aa_length": 539,
"aa_ref": "E",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1820,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1620,
"cds_start": 1435,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "ENST00000928693.1",
"gene_hgnc_id": 16627,
"gene_symbol": "CHEK2",
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
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