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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: 5-132703040-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=132703040&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 132703040,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001300791.2",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1492A>G",
"hgvs_p": "p.Lys498Glu",
"transcript": "NM_001300791.2",
"protein_id": "NP_001287720.1",
"transcript_support_level": null,
"aa_start": 498,
"aa_end": null,
"aa_length": 726,
"cds_start": 1492,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000403231.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300791.2"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1492A>G",
"hgvs_p": "p.Lys498Glu",
"transcript": "ENST00000403231.6",
"protein_id": "ENSP00000385808.1",
"transcript_support_level": 2,
"aa_start": 498,
"aa_end": null,
"aa_length": 726,
"cds_start": 1492,
"cds_end": null,
"cds_length": 2181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001300791.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000403231.6"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1420A>G",
"hgvs_p": "p.Lys474Glu",
"transcript": "ENST00000378735.5",
"protein_id": "ENSP00000368009.1",
"transcript_support_level": 1,
"aa_start": 474,
"aa_end": null,
"aa_length": 702,
"cds_start": 1420,
"cds_end": null,
"cds_length": 2109,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000378735.5"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1489A>G",
"hgvs_p": "p.Lys497Glu",
"transcript": "ENST00000618515.4",
"protein_id": "ENSP00000483023.1",
"transcript_support_level": 5,
"aa_start": 497,
"aa_end": null,
"aa_length": 725,
"cds_start": 1489,
"cds_end": null,
"cds_length": 2178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000618515.4"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1483A>G",
"hgvs_p": "p.Lys495Glu",
"transcript": "ENST00000875777.1",
"protein_id": "ENSP00000545836.1",
"transcript_support_level": null,
"aa_start": 495,
"aa_end": null,
"aa_length": 723,
"cds_start": 1483,
"cds_end": null,
"cds_length": 2172,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000875777.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1420A>G",
"hgvs_p": "p.Lys474Glu",
"transcript": "NM_001300792.2",
"protein_id": "NP_001287721.1",
"transcript_support_level": null,
"aa_start": 474,
"aa_end": null,
"aa_length": 702,
"cds_start": 1420,
"cds_end": null,
"cds_length": 2109,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001300792.2"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1411A>G",
"hgvs_p": "p.Lys471Glu",
"transcript": "NM_007054.7",
"protein_id": "NP_008985.3",
"transcript_support_level": null,
"aa_start": 471,
"aa_end": null,
"aa_length": 699,
"cds_start": 1411,
"cds_end": null,
"cds_length": 2100,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_007054.7"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1411A>G",
"hgvs_p": "p.Lys471Glu",
"transcript": "ENST00000378746.8",
"protein_id": "ENSP00000368020.3",
"transcript_support_level": 5,
"aa_start": 471,
"aa_end": null,
"aa_length": 699,
"cds_start": 1411,
"cds_end": null,
"cds_length": 2100,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000378746.8"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1408A>G",
"hgvs_p": "p.Lys470Glu",
"transcript": "ENST00000928467.1",
"protein_id": "ENSP00000598526.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 698,
"cds_start": 1408,
"cds_end": null,
"cds_length": 2097,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928467.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1411A>G",
"hgvs_p": "p.Lys471Glu",
"transcript": "ENST00000928468.1",
"protein_id": "ENSP00000598527.1",
"transcript_support_level": null,
"aa_start": 471,
"aa_end": null,
"aa_length": 676,
"cds_start": 1411,
"cds_end": null,
"cds_length": 2031,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928468.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1492A>G",
"hgvs_p": "p.Lys498Glu",
"transcript": "XM_006714526.5",
"protein_id": "XP_006714589.1",
"transcript_support_level": null,
"aa_start": 498,
"aa_end": null,
"aa_length": 724,
"cds_start": 1492,
"cds_end": null,
"cds_length": 2175,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006714526.5"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.1411A>G",
"hgvs_p": "p.Lys471Glu",
"transcript": "XM_017008996.3",
"protein_id": "XP_016864485.1",
"transcript_support_level": null,
"aa_start": 471,
"aa_end": null,
"aa_length": 697,
"cds_start": 1411,
"cds_end": null,
"cds_length": 2094,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017008996.3"
},
{
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "n.174A>G",
"hgvs_p": null,
"transcript": "ENST00000487055.1",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000487055.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ENSG00000230612",
"gene_hgnc_id": null,
"hgvs_c": "n.273+13206T>C",
"hgvs_p": null,
"transcript": "ENST00000431165.1",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000431165.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000230612",
"gene_hgnc_id": null,
"hgvs_c": "n.111+13206T>C",
"hgvs_p": null,
"transcript": "ENST00000628061.1",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000628061.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"hgvs_c": "c.-6A>G",
"hgvs_p": null,
"transcript": "ENST00000450441.5",
"protein_id": "ENSP00000405619.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 185,
"cds_start": null,
"cds_end": null,
"cds_length": 558,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000450441.5"
}
],
"gene_symbol": "KIF3A",
"gene_hgnc_id": 6319,
"dbsnp": "rs759731870",
"frequency_reference_population": 0.000038460727,
"hom_count_reference_population": 0,
"allele_count_reference_population": 62,
"gnomad_exomes_af": 0.0000397304,
"gnomad_genomes_af": 0.0000262822,
"gnomad_exomes_ac": 58,
"gnomad_genomes_ac": 4,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5027873516082764,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.354,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.7991,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.23,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 8.017,
"phylop100way_prediction": "Pathogenic",
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BS2",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BS2"
],
"verdict": "Likely_benign",
"transcript": "NM_001300791.2",
"gene_symbol": "KIF3A",
"hgnc_id": 6319,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1492A>G",
"hgvs_p": "p.Lys498Glu"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000431165.1",
"gene_symbol": "ENSG00000230612",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.273+13206T>C",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}