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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: 2-19937881-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=19937881&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 19937881,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000281405.9",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.2162G>C",
"hgvs_p": "p.Arg721Pro",
"transcript": "NM_001006657.2",
"protein_id": "NP_001006658.1",
"transcript_support_level": null,
"aa_start": 721,
"aa_end": null,
"aa_length": 1181,
"cds_start": 2162,
"cds_end": null,
"cds_length": 3546,
"cdna_start": 2252,
"cdna_end": null,
"cdna_length": 6931,
"mane_select": null,
"mane_plus": "ENST00000345530.8",
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.2162G>C",
"hgvs_p": "p.Arg721Pro",
"transcript": "ENST00000345530.8",
"protein_id": "ENSP00000314444.5",
"transcript_support_level": 1,
"aa_start": 721,
"aa_end": null,
"aa_length": 1181,
"cds_start": 2162,
"cds_end": null,
"cds_length": 3546,
"cdna_start": 2252,
"cdna_end": null,
"cdna_length": 6931,
"mane_select": null,
"mane_plus": "NM_001006657.2",
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.2129G>C",
"hgvs_p": "p.Arg710Pro",
"transcript": "NM_020779.4",
"protein_id": "NP_065830.2",
"transcript_support_level": null,
"aa_start": 710,
"aa_end": null,
"aa_length": 1170,
"cds_start": 2129,
"cds_end": null,
"cds_length": 3513,
"cdna_start": 2219,
"cdna_end": null,
"cdna_length": 6898,
"mane_select": "ENST00000281405.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.2129G>C",
"hgvs_p": "p.Arg710Pro",
"transcript": "ENST00000281405.9",
"protein_id": "ENSP00000281405.5",
"transcript_support_level": 1,
"aa_start": 710,
"aa_end": null,
"aa_length": 1170,
"cds_start": 2129,
"cds_end": null,
"cds_length": 3513,
"cdna_start": 2219,
"cdna_end": null,
"cdna_length": 6898,
"mane_select": "NM_020779.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.767G>C",
"hgvs_p": "p.Arg256Pro",
"transcript": "ENST00000453014.1",
"protein_id": "ENSP00000404409.1",
"transcript_support_level": 1,
"aa_start": 256,
"aa_end": null,
"aa_length": 406,
"cds_start": 767,
"cds_end": null,
"cds_length": 1221,
"cdna_start": 767,
"cdna_end": null,
"cdna_length": 1624,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.857G>C",
"hgvs_p": "p.Arg286Pro",
"transcript": "XM_011533007.3",
"protein_id": "XP_011531309.1",
"transcript_support_level": null,
"aa_start": 286,
"aa_end": null,
"aa_length": 746,
"cds_start": 857,
"cds_end": null,
"cds_length": 2241,
"cdna_start": 962,
"cdna_end": null,
"cdna_length": 5641,
"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": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "n.2162G>C",
"hgvs_p": null,
"transcript": "ENST00000414212.5",
"protein_id": "ENSP00000390802.1",
"transcript_support_level": 5,
"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": 3483,
"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": 13,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "n.*853G>C",
"hgvs_p": null,
"transcript": "ENST00000445063.5",
"protein_id": "ENSP00000390105.1",
"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": 2788,
"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": 19,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "n.2219G>C",
"hgvs_p": null,
"transcript": "XR_426989.4",
"protein_id": null,
"transcript_support_level": null,
"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": 3061,
"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": 13,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "n.*853G>C",
"hgvs_p": null,
"transcript": "ENST00000445063.5",
"protein_id": "ENSP00000390105.1",
"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": 2788,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"hgvs_c": "c.*51G>C",
"hgvs_p": null,
"transcript": "XM_047445199.1",
"protein_id": "XP_047301155.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 673,
"cds_start": -4,
"cds_end": null,
"cds_length": 2022,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2216,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "WDR35",
"gene_hgnc_id": 29250,
"dbsnp": "rs370797645",
"frequency_reference_population": 0.0000013681425,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000136814,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.8715973496437073,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.65,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.8286,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.2,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 1.736,
"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": 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": "ENST00000281405.9",
"gene_symbol": "WDR35",
"hgnc_id": 29250,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2129G>C",
"hgvs_p": "p.Arg710Pro"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}