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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: 14-67748470-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=67748470&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 67748470,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000347230.9",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "R",
"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.7586C>G",
"hgvs_p": "p.Pro2529Arg",
"transcript": "NM_015346.4",
"protein_id": "NP_056161.2",
"transcript_support_level": null,
"aa_start": 2529,
"aa_end": null,
"aa_length": 2539,
"cds_start": 7586,
"cds_end": null,
"cds_length": 7620,
"cdna_start": 7726,
"cdna_end": null,
"cdna_length": 9674,
"mane_select": "ENST00000347230.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"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.7586C>G",
"hgvs_p": "p.Pro2529Arg",
"transcript": "ENST00000347230.9",
"protein_id": "ENSP00000251119.5",
"transcript_support_level": 1,
"aa_start": 2529,
"aa_end": null,
"aa_length": 2539,
"cds_start": 7586,
"cds_end": null,
"cds_length": 7620,
"cdna_start": 7726,
"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.8341C>G",
"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.*5564C>G",
"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.*5564C>G",
"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": "P",
"aa_alt": "R",
"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.7631C>G",
"hgvs_p": "p.Pro2544Arg",
"transcript": "ENST00000678386.1",
"protein_id": "ENSP00000503677.1",
"transcript_support_level": null,
"aa_start": 2544,
"aa_end": null,
"aa_length": 2554,
"cds_start": 7631,
"cds_end": null,
"cds_length": 7665,
"cdna_start": 7771,
"cdna_end": null,
"cdna_length": 9719,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"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.7604C>G",
"hgvs_p": "p.Pro2535Arg",
"transcript": "ENST00000676512.1",
"protein_id": "ENSP00000504552.1",
"transcript_support_level": null,
"aa_start": 2535,
"aa_end": null,
"aa_length": 2545,
"cds_start": 7604,
"cds_end": null,
"cds_length": 7638,
"cdna_start": 7744,
"cdna_end": null,
"cdna_length": 9692,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"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.7508C>G",
"hgvs_p": "p.Pro2503Arg",
"transcript": "ENST00000676620.1",
"protein_id": "ENSP00000504587.1",
"transcript_support_level": null,
"aa_start": 2503,
"aa_end": null,
"aa_length": 2513,
"cds_start": 7508,
"cds_end": null,
"cds_length": 7542,
"cdna_start": 7648,
"cdna_end": null,
"cdna_length": 9596,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"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.5261C>G",
"hgvs_p": "p.Pro1754Arg",
"transcript": "XM_047431174.1",
"protein_id": "XP_047287130.1",
"transcript_support_level": null,
"aa_start": 1754,
"aa_end": null,
"aa_length": 1764,
"cds_start": 5261,
"cds_end": null,
"cds_length": 5295,
"cdna_start": 5432,
"cdna_end": null,
"cdna_length": 7380,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "R",
"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.5168C>G",
"hgvs_p": "p.Pro1723Arg",
"transcript": "XM_047431175.1",
"protein_id": "XP_047287131.1",
"transcript_support_level": null,
"aa_start": 1723,
"aa_end": null,
"aa_length": 1733,
"cds_start": 5168,
"cds_end": null,
"cds_length": 5202,
"cdna_start": 5275,
"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+2582C>G",
"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+2582C>G",
"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": "rs143198225",
"frequency_reference_population": 0.0009076863,
"hom_count_reference_population": 15,
"allele_count_reference_population": 1464,
"gnomad_exomes_af": 0.000507349,
"gnomad_genomes_af": 0.0047454,
"gnomad_exomes_ac": 741,
"gnomad_genomes_ac": 723,
"gnomad_exomes_homalt": 7,
"gnomad_genomes_homalt": 8,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.002698242664337158,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.062,
"revel_prediction": "Benign",
"alphamissense_score": 0.0759,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.74,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.368,
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000347230.9",
"gene_symbol": "ZFYVE26",
"hgnc_id": 20761,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.7586C>G",
"hgvs_p": "p.Pro2529Arg"
}
],
"clinvar_disease": "Hereditary spastic paraplegia,Hereditary spastic paraplegia 15,Spastic paraplegia,not provided",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:3 B:3",
"phenotype_combined": "Hereditary spastic paraplegia 15|Spastic paraplegia|not provided|Hereditary spastic paraplegia",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}