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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: 7-41972561-GT-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=41972561&ref=GT&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 41972561,
"ref": "GT",
"alt": "G",
"effect": "frameshift_variant",
"transcript": "ENST00000395925.8",
"consequences": [
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "NM_000168.6",
"protein_id": "NP_000159.3",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2159,
"cdna_end": null,
"cdna_length": 8405,
"mane_select": "ENST00000395925.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "ENST00000395925.8",
"protein_id": "ENSP00000379258.3",
"transcript_support_level": 5,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2159,
"cdna_end": null,
"cdna_length": 8405,
"mane_select": "NM_000168.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "ENST00000677605.1",
"protein_id": "ENSP00000503743.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 1977,
"cdna_end": null,
"cdna_length": 8223,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "ENST00000678429.1",
"protein_id": "ENSP00000502957.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 1991,
"cdna_end": null,
"cdna_length": 8237,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1704delA",
"hgvs_p": "p.Lys568fs",
"transcript": "ENST00000677288.1",
"protein_id": "ENSP00000503986.1",
"transcript_support_level": null,
"aa_start": 568,
"aa_end": null,
"aa_length": 1522,
"cds_start": 1704,
"cds_end": null,
"cds_length": 4569,
"cdna_start": 1835,
"cdna_end": null,
"cdna_length": 8081,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1701delA",
"hgvs_p": "p.Lys567fs",
"transcript": "ENST00000479210.1",
"protein_id": "ENSP00000496377.1",
"transcript_support_level": 2,
"aa_start": 567,
"aa_end": null,
"aa_length": 1521,
"cds_start": 1701,
"cds_end": null,
"cds_length": 4566,
"cdna_start": 1855,
"cdna_end": null,
"cdna_length": 4968,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "XM_047420205.1",
"protein_id": "XP_047276161.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2078,
"cdna_end": null,
"cdna_length": 8324,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "XM_047420206.1",
"protein_id": "XP_047276162.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 10009,
"cdna_end": null,
"cdna_length": 16255,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "XM_047420207.1",
"protein_id": "XP_047276163.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2041,
"cdna_end": null,
"cdna_length": 8287,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "XM_047420208.1",
"protein_id": "XP_047276164.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2195,
"cdna_end": null,
"cdna_length": 8441,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs",
"transcript": "XM_047420209.1",
"protein_id": "XP_047276165.1",
"transcript_support_level": null,
"aa_start": 626,
"aa_end": null,
"aa_length": 1580,
"cds_start": 1878,
"cds_end": null,
"cds_length": 4743,
"cdna_start": 2009,
"cdna_end": null,
"cdna_length": 8255,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1875delA",
"hgvs_p": "p.Lys625fs",
"transcript": "XM_017011997.2",
"protein_id": "XP_016867486.1",
"transcript_support_level": null,
"aa_start": 625,
"aa_end": null,
"aa_length": 1579,
"cds_start": 1875,
"cds_end": null,
"cds_length": 4740,
"cdna_start": 11850,
"cdna_end": null,
"cdna_length": 18096,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "K",
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"frameshift_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "c.1701delA",
"hgvs_p": "p.Lys567fs",
"transcript": "XM_011515274.3",
"protein_id": "XP_011513576.1",
"transcript_support_level": null,
"aa_start": 567,
"aa_end": null,
"aa_length": 1521,
"cds_start": 1701,
"cds_end": null,
"cds_length": 4566,
"cdna_start": 1855,
"cdna_end": null,
"cdna_length": 8101,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"hgvs_c": "n.431delA",
"hgvs_p": null,
"transcript": "ENST00000464291.1",
"protein_id": null,
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 553,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "GLI3",
"gene_hgnc_id": 4319,
"dbsnp": "rs1554306093",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": null,
"computational_prediction_selected": null,
"computational_source_selected": null,
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 1.465,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"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": 12,
"acmg_classification": "Pathogenic",
"acmg_criteria": "PVS1,PM2,PP5_Moderate",
"acmg_by_gene": [
{
"score": 12,
"benign_score": 0,
"pathogenic_score": 12,
"criteria": [
"PVS1",
"PM2",
"PP5_Moderate"
],
"verdict": "Pathogenic",
"transcript": "ENST00000395925.8",
"gene_symbol": "GLI3",
"hgnc_id": 4319,
"effects": [
"frameshift_variant"
],
"inheritance_mode": "AD,AR",
"hgvs_c": "c.1878delA",
"hgvs_p": "p.Lys626fs"
}
],
"clinvar_disease": "Greig cephalopolysyndactyly syndrome,Pallister-Hall syndrome",
"clinvar_classification": "Pathogenic",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "P:1",
"phenotype_combined": "Pallister-Hall syndrome;Greig cephalopolysyndactyly syndrome",
"pathogenicity_classification_combined": "Pathogenic",
"custom_annotations": null
}
],
"message": null
}