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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: 14-67748497-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=67748497&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 67748497,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000347230.9",
"consequences": [
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7559G>C",
"hgvs_p": "p.Cys2520Ser",
"transcript": "NM_015346.4",
"protein_id": "NP_056161.2",
"transcript_support_level": null,
"aa_start": 2520,
"aa_end": null,
"aa_length": 2539,
"cds_start": 7559,
"cds_end": null,
"cds_length": 7620,
"cdna_start": 7699,
"cdna_end": null,
"cdna_length": 9674,
"mane_select": "ENST00000347230.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7559G>C",
"hgvs_p": "p.Cys2520Ser",
"transcript": "ENST00000347230.9",
"protein_id": "ENSP00000251119.5",
"transcript_support_level": 1,
"aa_start": 2520,
"aa_end": null,
"aa_length": 2539,
"cds_start": 7559,
"cds_end": null,
"cds_length": 7620,
"cdna_start": 7699,
"cdna_end": null,
"cdna_length": 9674,
"mane_select": "NM_015346.4",
"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": 41,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "n.8314G>C",
"hgvs_p": null,
"transcript": "ENST00000554523.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 8582,
"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": 40,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "n.*5537G>C",
"hgvs_p": null,
"transcript": "ENST00000554557.5",
"protein_id": "ENSP00000450431.1",
"transcript_support_level": 1,
"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": 7466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 40,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "n.*5537G>C",
"hgvs_p": null,
"transcript": "ENST00000554557.5",
"protein_id": "ENSP00000450431.1",
"transcript_support_level": 1,
"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": 7466,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7604G>C",
"hgvs_p": "p.Cys2535Ser",
"transcript": "ENST00000678386.1",
"protein_id": "ENSP00000503677.1",
"transcript_support_level": null,
"aa_start": 2535,
"aa_end": null,
"aa_length": 2554,
"cds_start": 7604,
"cds_end": null,
"cds_length": 7665,
"cdna_start": 7744,
"cdna_end": null,
"cdna_length": 9719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7577G>C",
"hgvs_p": "p.Cys2526Ser",
"transcript": "ENST00000676512.1",
"protein_id": "ENSP00000504552.1",
"transcript_support_level": null,
"aa_start": 2526,
"aa_end": null,
"aa_length": 2545,
"cds_start": 7577,
"cds_end": null,
"cds_length": 7638,
"cdna_start": 7717,
"cdna_end": null,
"cdna_length": 9692,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 42,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7481G>C",
"hgvs_p": "p.Cys2494Ser",
"transcript": "ENST00000676620.1",
"protein_id": "ENSP00000504587.1",
"transcript_support_level": null,
"aa_start": 2494,
"aa_end": null,
"aa_length": 2513,
"cds_start": 7481,
"cds_end": null,
"cds_length": 7542,
"cdna_start": 7621,
"cdna_end": null,
"cdna_length": 9596,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.5234G>C",
"hgvs_p": "p.Cys1745Ser",
"transcript": "XM_047431174.1",
"protein_id": "XP_047287130.1",
"transcript_support_level": null,
"aa_start": 1745,
"aa_end": null,
"aa_length": 1764,
"cds_start": 5234,
"cds_end": null,
"cds_length": 5295,
"cdna_start": 5405,
"cdna_end": null,
"cdna_length": 7380,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "C",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.5141G>C",
"hgvs_p": "p.Cys1714Ser",
"transcript": "XM_047431175.1",
"protein_id": "XP_047287131.1",
"transcript_support_level": null,
"aa_start": 1714,
"aa_end": null,
"aa_length": 1733,
"cds_start": 5141,
"cds_end": null,
"cds_length": 5202,
"cdna_start": 5248,
"cdna_end": null,
"cdna_length": 7223,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "n.2679+2555G>C",
"hgvs_p": null,
"transcript": "ENST00000394455.6",
"protein_id": null,
"transcript_support_level": 2,
"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": 4134,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": 41,
"intron_rank_end": null,
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"hgvs_c": "c.7416+2555G>C",
"hgvs_p": null,
"transcript": "XM_047431173.1",
"protein_id": "XP_047287129.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2497,
"cds_start": -4,
"cds_end": null,
"cds_length": 7494,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8484,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "ZFYVE26",
"gene_hgnc_id": 20761,
"dbsnp": "rs1555392769",
"frequency_reference_population": 0.0000061589167,
"hom_count_reference_population": 0,
"allele_count_reference_population": 9,
"gnomad_exomes_af": 0.00000615892,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 9,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.9219850301742554,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.564,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.8188,
"alphamissense_prediction": "Pathogenic",
"bayesdelnoaf_score": 0.24,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.474,
"phylop100way_prediction": "Uncertain_significance",
"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": 4,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,PP3_Moderate",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 0,
"pathogenic_score": 4,
"criteria": [
"PM2",
"PP3_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000347230.9",
"gene_symbol": "ZFYVE26",
"hgnc_id": 20761,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.7559G>C",
"hgvs_p": "p.Cys2520Ser"
}
],
"clinvar_disease": "Spastic paraplegia",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "Spastic paraplegia",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}