← Back to variant description
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: 11-132529107-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=132529107&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 8,
"criteria": [
"BP4_Moderate",
"BP6",
"BP7",
"BS2"
],
"effects": [
"synonymous_variant"
],
"gene_symbol": "OPCML",
"hgnc_id": 8143,
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -8,
"transcript": "NM_001319103.2",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Moderate,BP6,BP7,BS2",
"acmg_score": -8,
"allele_count_reference_population": 1138,
"alphamissense_prediction": null,
"alphamissense_score": null,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.46,
"chr": "11",
"clinvar_classification": "Likely benign",
"clinvar_disease": "OPCML-related disorder",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"computational_prediction_selected": "Benign",
"computational_score_selected": -0.46000000834465027,
"computational_source_selected": "BayesDel_noAF",
"consequences": [
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 338,
"aa_ref": "I",
"aa_start": 153,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6406,
"cdna_start": 636,
"cds_end": null,
"cds_length": 1017,
"cds_start": 459,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001012393.5",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.459T>C",
"hgvs_p": "p.Ile153Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000524381.6",
"protein_coding": true,
"protein_id": "NP_001012393.1",
"strand": false,
"transcript": "NM_001012393.5",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 338,
"aa_ref": "I",
"aa_start": 153,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 6406,
"cdna_start": 636,
"cds_end": null,
"cds_length": 1017,
"cds_start": 459,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000524381.6",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.459T>C",
"hgvs_p": "p.Ile153Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001012393.5",
"protein_coding": true,
"protein_id": "ENSP00000434750.1",
"strand": false,
"transcript": "ENST00000524381.6",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 345,
"aa_ref": "I",
"aa_start": 160,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6833,
"cdna_start": 1059,
"cds_end": null,
"cds_length": 1038,
"cds_start": 480,
"consequences": [
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000331898.11",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000330862.7",
"strand": false,
"transcript": "ENST00000331898.11",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 304,
"aa_ref": "I",
"aa_start": 119,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1302,
"cdna_start": 571,
"cds_end": null,
"cds_length": 915,
"cds_start": 357,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000374778.4",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.357T>C",
"hgvs_p": "p.Ile119Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000363910.4",
"strand": false,
"transcript": "ENST00000374778.4",
"transcript_support_level": 1
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 354,
"aa_ref": "I",
"aa_start": 160,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7021,
"cdna_start": 1224,
"cds_end": null,
"cds_length": 1065,
"cds_start": 480,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001319103.2",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001306032.1",
"strand": false,
"transcript": "NM_001319103.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 354,
"aa_ref": "I",
"aa_start": 160,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 7021,
"cdna_start": 1224,
"cds_end": null,
"cds_length": 1065,
"cds_start": 480,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000541867.6",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000445496.1",
"strand": false,
"transcript": "ENST00000541867.6",
"transcript_support_level": 5
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 345,
"aa_ref": "I",
"aa_start": 160,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6994,
"cdna_start": 1224,
"cds_end": null,
"cds_length": 1038,
"cds_start": 480,
"consequences": [
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_002545.5",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_002536.1",
"strand": false,
"transcript": "NM_002545.5",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 344,
"aa_ref": "I",
"aa_start": 160,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6991,
"cdna_start": 1224,
"cds_end": null,
"cds_length": 1035,
"cds_start": 480,
"consequences": [
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001319106.2",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.480T>C",
"hgvs_p": "p.Ile160Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001306035.1",
"strand": false,
"transcript": "NM_001319106.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 304,
"aa_ref": "I",
"aa_start": 119,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6409,
"cdna_start": 639,
"cds_end": null,
"cds_length": 915,
"cds_start": 357,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "NM_001319105.2",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.357T>C",
"hgvs_p": "p.Ile119Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001306034.1",
"strand": false,
"transcript": "NM_001319105.2",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 245,
"aa_ref": "I",
"aa_start": 60,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6321,
"cdna_start": 551,
"cds_end": null,
"cds_length": 738,
"cds_start": 180,
"consequences": [
"synonymous_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "NM_001319104.4",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.180T>C",
"hgvs_p": "p.Ile60Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001306033.1",
"strand": false,
"transcript": "NM_001319104.4",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 337,
"aa_ref": "I",
"aa_start": 153,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6403,
"cdna_start": 636,
"cds_end": null,
"cds_length": 1014,
"cds_start": 459,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "XM_006718846.4",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.459T>C",
"hgvs_p": "p.Ile153Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006718909.1",
"strand": false,
"transcript": "XM_006718846.4",
"transcript_support_level": null
},
{
"aa_alt": "I",
"aa_end": null,
"aa_length": 304,
"aa_ref": "I",
"aa_start": 119,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6323,
"cdna_start": 553,
"cds_end": null,
"cds_length": 915,
"cds_start": 357,
"consequences": [
"synonymous_variant"
],
"exon_count": 8,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "XM_047427032.1",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "c.357T>C",
"hgvs_p": "p.Ile119Ile",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047282988.1",
"strand": false,
"transcript": "XM_047427032.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 1343,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 7,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000529038.5",
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"hgvs_c": "n.452T>C",
"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": "ENST00000529038.5",
"transcript_support_level": 5
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs145182728",
"effect": "synonymous_variant",
"frequency_reference_population": 0.0007052894,
"gene_hgnc_id": 8143,
"gene_symbol": "OPCML",
"gnomad_exomes_ac": 1070,
"gnomad_exomes_af": 0.00073226,
"gnomad_exomes_homalt": 2,
"gnomad_genomes_ac": 68,
"gnomad_genomes_af": 0.000446511,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 2,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Likely benign",
"phenotype_combined": "OPCML-related disorder",
"phylop100way_prediction": "Benign",
"phylop100way_score": 0.596,
"pos": 132529107,
"ref": "A",
"revel_prediction": null,
"revel_score": null,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_001319103.2"
}
]
}