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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: X-71224281-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=71224281&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 71224281,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000361726.7",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "NM_000166.6",
"protein_id": "NP_000157.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 702,
"cdna_end": null,
"cdna_length": 1937,
"mane_select": "ENST00000361726.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000361726.7",
"protein_id": "ENSP00000354900.6",
"transcript_support_level": 1,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 702,
"cdna_end": null,
"cdna_length": 1937,
"mane_select": "NM_000166.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "NM_001097642.3",
"protein_id": "NP_001091111.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 642,
"cdna_end": null,
"cdna_length": 1877,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "NM_001440770.1",
"protein_id": "NP_001427699.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 825,
"cdna_end": null,
"cdna_length": 2060,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000374029.2",
"protein_id": "ENSP00000363141.1",
"transcript_support_level": 5,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 706,
"cdna_end": null,
"cdna_length": 1625,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000447581.2",
"protein_id": "ENSP00000407223.2",
"transcript_support_level": 5,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 805,
"cdna_end": null,
"cdna_length": 2040,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000645009.2",
"protein_id": "ENSP00000494142.2",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 834,
"cdna_end": null,
"cdna_length": 2069,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000646835.1",
"protein_id": "ENSP00000494596.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 941,
"cdna_end": null,
"cdna_length": 1860,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000647424.1",
"protein_id": "ENSP00000495960.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 669,
"cdna_end": null,
"cdna_length": 1603,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000674549.1",
"protein_id": "ENSP00000502766.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 625,
"cdna_end": null,
"cdna_length": 1860,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000674844.1",
"protein_id": "ENSP00000502556.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 703,
"cdna_end": null,
"cdna_length": 1938,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000675209.1",
"protein_id": "ENSP00000501813.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 851,
"cdna_end": null,
"cdna_length": 2086,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000675368.1",
"protein_id": "ENSP00000501757.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 2639,
"cdna_end": null,
"cdna_length": 3874,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe",
"transcript": "ENST00000675609.1",
"protein_id": "ENSP00000501571.1",
"transcript_support_level": null,
"aa_start": 192,
"aa_end": null,
"aa_length": 283,
"cds_start": 574,
"cds_end": null,
"cds_length": 852,
"cdna_start": 796,
"cdna_end": null,
"cdna_length": 1717,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "GJB1",
"gene_hgnc_id": 4283,
"dbsnp": "rs771579861",
"frequency_reference_population": 0.000005475327,
"hom_count_reference_population": 3,
"allele_count_reference_population": 6,
"gnomad_exomes_af": 0.00000547533,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 6,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.91124427318573,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.764,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.1648,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.59,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 5.566,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.01,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": 1,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM1,PP2,PP3_Moderate,BS2",
"acmg_by_gene": [
{
"score": 1,
"benign_score": 4,
"pathogenic_score": 5,
"criteria": [
"PM1",
"PP2",
"PP3_Moderate",
"BS2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000361726.7",
"gene_symbol": "GJB1",
"hgnc_id": 4283,
"effects": [
"missense_variant"
],
"inheritance_mode": "XL",
"hgvs_c": "c.574G>T",
"hgvs_p": "p.Val192Phe"
}
],
"clinvar_disease": "Charcot-Marie-Tooth Neuropathy X,Charcot-Marie-Tooth disease,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "Charcot-Marie-Tooth disease|not specified|Charcot-Marie-Tooth Neuropathy X",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}