← 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: 6-138865022-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=138865022&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 12,
"criteria": [
"BP4_Strong",
"BS1",
"BS2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "ECT2L",
"hgnc_id": 21118,
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"inheritance_mode": "AR",
"pathogenic_score": 0,
"score": -12,
"transcript": "NM_001077706.3",
"verdict": "Benign"
}
],
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BS1,BS2",
"acmg_score": -12,
"allele_count_reference_population": 6255,
"alphamissense_prediction": null,
"alphamissense_score": 0.0499,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Benign",
"bayesdelnoaf_score": -0.59,
"chr": "6",
"clinvar_classification": "not provided",
"clinvar_disease": "not specified",
"clinvar_review_status": "no classification provided",
"clinvar_submissions_summary": "O:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.0023939907550811768,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 904,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4507,
"cdna_start": 1667,
"cds_end": null,
"cds_length": 2715,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001077706.3",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000541398.7",
"protein_coding": true,
"protein_id": "NP_001071174.1",
"strand": true,
"transcript": "NM_001077706.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 904,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 4507,
"cdna_start": 1667,
"cds_end": null,
"cds_length": 2715,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000541398.7",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_001077706.3",
"protein_coding": true,
"protein_id": "ENSP00000442307.2",
"strand": true,
"transcript": "ENST00000541398.7",
"transcript_support_level": 5
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 904,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4343,
"cdna_start": 1503,
"cds_end": null,
"cds_length": 2715,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001195037.2",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001181966.1",
"strand": true,
"transcript": "NM_001195037.2",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 904,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4343,
"cdna_start": 1503,
"cds_end": null,
"cds_length": 2715,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 21,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000367682.6",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000356655.2",
"strand": true,
"transcript": "ENST00000367682.6",
"transcript_support_level": 5
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 946,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4633,
"cdna_start": 1667,
"cds_end": null,
"cds_length": 2841,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_006715472.4",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006715535.1",
"strand": true,
"transcript": "XM_006715472.4",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 946,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4493,
"cdna_start": 1527,
"cds_end": null,
"cds_length": 2841,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_011535795.3",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011534097.1",
"strand": true,
"transcript": "XM_011535795.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 946,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4595,
"cdna_start": 1629,
"cds_end": null,
"cds_length": 2841,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 23,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_017010828.2",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866317.1",
"strand": true,
"transcript": "XM_017010828.2",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 915,
"aa_ref": "W",
"aa_start": 409,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4540,
"cdna_start": 1574,
"cds_end": null,
"cds_length": 2748,
"cds_start": 1225,
"consequences": [
"missense_variant"
],
"exon_count": 22,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_017010829.2",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1225T>G",
"hgvs_p": "p.Trp409Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866318.1",
"strand": true,
"transcript": "XM_017010829.2",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 877,
"aa_ref": "W",
"aa_start": 371,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4169,
"cdna_start": 1203,
"cds_end": null,
"cds_length": 2634,
"cds_start": 1111,
"consequences": [
"missense_variant"
],
"exon_count": 20,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "XM_011535797.3",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1111T>G",
"hgvs_p": "p.Trp371Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011534099.1",
"strand": true,
"transcript": "XM_011535797.3",
"transcript_support_level": null
},
{
"aa_alt": "G",
"aa_end": null,
"aa_length": 603,
"aa_ref": "W",
"aa_start": 440,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2180,
"cdna_start": 1667,
"cds_end": null,
"cds_length": 1812,
"cds_start": 1318,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_017010830.2",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "c.1318T>G",
"hgvs_p": "p.Trp440Gly",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016866319.1",
"strand": true,
"transcript": "XM_017010830.2",
"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": 649,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 6,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "ENST00000495970.1",
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"hgvs_c": "n.306T>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "ENST00000495970.1",
"transcript_support_level": 3
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs79294486",
"effect": "missense_variant",
"frequency_reference_population": 0.0038767618,
"gene_hgnc_id": 21118,
"gene_symbol": "ECT2L",
"gnomad_exomes_ac": 3965,
"gnomad_exomes_af": 0.00271368,
"gnomad_exomes_homalt": 57,
"gnomad_genomes_ac": 2290,
"gnomad_genomes_af": 0.015032,
"gnomad_genomes_homalt": 41,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 98,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "not provided",
"phenotype_combined": "not specified",
"phylop100way_prediction": "Benign",
"phylop100way_score": -0.617,
"pos": 138865022,
"ref": "T",
"revel_prediction": "Benign",
"revel_score": 0.114,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0.019999999552965164,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0.02,
"transcript": "NM_001077706.3"
}
]
}