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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: 11-65871185-AT-GC (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=65871185&ref=AT&alt=GC&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 0,
"criteria": [],
"effects": [
"missense_variant"
],
"gene_symbol": "EFEMP2",
"hgnc_id": 3219,
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"inheritance_mode": "AR,AD",
"pathogenic_score": 0,
"score": 0,
"transcript": "NM_016938.5",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "",
"acmg_score": 0,
"allele_count_reference_population": 0,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "GC",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": null,
"bayesdelnoaf_score": null,
"chr": "11",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": null,
"computational_score_selected": null,
"computational_source_selected": null,
"consequences": [
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1934,
"cdna_start": 464,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NM_016938.5",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000307998.11",
"protein_coding": true,
"protein_id": "NP_058634.4",
"strand": false,
"transcript": "NM_016938.5",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1934,
"cdna_start": 464,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000307998.11",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_016938.5",
"protein_coding": true,
"protein_id": "ENSP00000309953.6",
"strand": false,
"transcript": "ENST00000307998.11",
"transcript_support_level": 1
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "retained_intron",
"canonical": false,
"cdna_end": null,
"cdna_length": 1562,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 4,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000527969.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "n.17_18delATinsGC",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000527969.1",
"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": 1813,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 12,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000531972.5",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "n.338_339delATinsGC",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000435295.1",
"strand": false,
"transcript": "ENST00000531972.5",
"transcript_support_level": 1
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 516,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1718,
"cdna_start": 433,
"cds_end": null,
"cds_length": 1551,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907927.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577986.1",
"strand": false,
"transcript": "ENST00000907927.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 471,
"aa_ref": "Y",
"aa_start": 141,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2049,
"cdna_start": 586,
"cds_end": null,
"cds_length": 1416,
"cds_start": 422,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947418.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.422_423delATinsGC",
"hgvs_p": "p.Tyr141Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617477.1",
"strand": false,
"transcript": "ENST00000947418.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 445,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1588,
"cdna_start": 493,
"cds_end": null,
"cds_length": 1338,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907924.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577983.1",
"strand": false,
"transcript": "ENST00000907924.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1933,
"cdna_start": 469,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907916.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577975.1",
"strand": false,
"transcript": "ENST00000907916.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2485,
"cdna_start": 1015,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907917.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577976.1",
"strand": false,
"transcript": "ENST00000907917.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1573,
"cdna_start": 494,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907918.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577977.1",
"strand": false,
"transcript": "ENST00000907918.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1936,
"cdna_start": 472,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907919.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577978.1",
"strand": false,
"transcript": "ENST00000907919.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1912,
"cdna_start": 448,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907920.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577979.1",
"strand": false,
"transcript": "ENST00000907920.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1900,
"cdna_start": 437,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907922.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577981.1",
"strand": false,
"transcript": "ENST00000907922.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1894,
"cdna_start": 433,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907923.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577982.1",
"strand": false,
"transcript": "ENST00000907923.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2365,
"cdna_start": 896,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947415.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617474.1",
"strand": false,
"transcript": "ENST00000947415.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2251,
"cdna_start": 782,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947416.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617475.1",
"strand": false,
"transcript": "ENST00000947416.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2015,
"cdna_start": 936,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947417.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617476.1",
"strand": false,
"transcript": "ENST00000947417.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 443,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1957,
"cdna_start": 492,
"cds_end": null,
"cds_length": 1332,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947419.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617478.1",
"strand": false,
"transcript": "ENST00000947419.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 442,
"aa_ref": "Y",
"aa_start": 112,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1910,
"cdna_start": 440,
"cds_end": null,
"cds_length": 1329,
"cds_start": 335,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000907921.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.335_336delATinsGC",
"hgvs_p": "p.Tyr112Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000577980.1",
"strand": false,
"transcript": "ENST00000907921.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 442,
"aa_ref": "Y",
"aa_start": 112,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1687,
"cdna_start": 604,
"cds_end": null,
"cds_length": 1329,
"cds_start": 335,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000947421.1",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.335_336delATinsGC",
"hgvs_p": "p.Tyr112Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000617480.1",
"strand": false,
"transcript": "ENST00000947421.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 436,
"aa_ref": "Y",
"aa_start": 113,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1504,
"cdna_start": 407,
"cds_end": null,
"cds_length": 1311,
"cds_start": 338,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": null,
"exon_rank_end": null,
"feature": "ENST00000528176.5",
"gene_hgnc_id": 3219,
"gene_symbol": "EFEMP2",
"hgvs_c": "c.338_339delATinsGC",
"hgvs_p": "p.Tyr113Cys",
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