← Back to variant description
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: 10-120589457-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=120589457&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 120589457,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000398250.6",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.771C>A",
"hgvs_p": "p.Ser257Arg",
"transcript": "NM_001030059.3",
"protein_id": "NP_001025230.1",
"transcript_support_level": null,
"aa_start": 257,
"aa_end": null,
"aa_length": 271,
"cds_start": 771,
"cds_end": null,
"cds_length": 816,
"cdna_start": 850,
"cdna_end": null,
"cdna_length": 3458,
"mane_select": "ENST00000398250.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.771C>A",
"hgvs_p": "p.Ser257Arg",
"transcript": "ENST00000398250.6",
"protein_id": "ENSP00000381302.1",
"transcript_support_level": 1,
"aa_start": 257,
"aa_end": null,
"aa_length": 271,
"cds_start": 771,
"cds_end": null,
"cds_length": 816,
"cdna_start": 850,
"cdna_end": null,
"cdna_length": 3458,
"mane_select": "NM_001030059.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.582C>A",
"hgvs_p": "p.Ser194Arg",
"transcript": "NM_001318167.2",
"protein_id": "NP_001305096.1",
"transcript_support_level": null,
"aa_start": 194,
"aa_end": null,
"aa_length": 208,
"cds_start": 582,
"cds_end": null,
"cds_length": 627,
"cdna_start": 661,
"cdna_end": null,
"cdna_length": 3269,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.765C>A",
"hgvs_p": "p.Ser255Arg",
"transcript": "XM_011539444.4",
"protein_id": "XP_011537746.1",
"transcript_support_level": null,
"aa_start": 255,
"aa_end": null,
"aa_length": 269,
"cds_start": 765,
"cds_end": null,
"cds_length": 810,
"cdna_start": 931,
"cdna_end": null,
"cdna_length": 3539,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.732C>A",
"hgvs_p": "p.Ser244Arg",
"transcript": "XM_047424709.1",
"protein_id": "XP_047280665.1",
"transcript_support_level": null,
"aa_start": 244,
"aa_end": null,
"aa_length": 258,
"cds_start": 732,
"cds_end": null,
"cds_length": 777,
"cdna_start": 792,
"cdna_end": null,
"cdna_length": 3400,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.600C>A",
"hgvs_p": "p.Ser200Arg",
"transcript": "XM_005269592.3",
"protein_id": "XP_005269649.1",
"transcript_support_level": null,
"aa_start": 200,
"aa_end": null,
"aa_length": 214,
"cds_start": 600,
"cds_end": null,
"cds_length": 645,
"cdna_start": 679,
"cdna_end": null,
"cdna_length": 3287,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.408C>A",
"hgvs_p": "p.Ser136Arg",
"transcript": "XM_017015821.3",
"protein_id": "XP_016871310.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 150,
"cds_start": 408,
"cds_end": null,
"cds_length": 453,
"cdna_start": 688,
"cdna_end": null,
"cdna_length": 3296,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.408C>A",
"hgvs_p": "p.Ser136Arg",
"transcript": "XM_017015822.2",
"protein_id": "XP_016871311.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 150,
"cds_start": 408,
"cds_end": null,
"cds_length": 453,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 3268,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.408C>A",
"hgvs_p": "p.Ser136Arg",
"transcript": "XM_024447862.2",
"protein_id": "XP_024303630.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 150,
"cds_start": 408,
"cds_end": null,
"cds_length": 453,
"cdna_start": 500,
"cdna_end": null,
"cdna_length": 3108,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.408C>A",
"hgvs_p": "p.Ser136Arg",
"transcript": "XM_047424710.1",
"protein_id": "XP_047280666.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 150,
"cds_start": 408,
"cds_end": null,
"cds_length": 453,
"cdna_start": 596,
"cdna_end": null,
"cdna_length": 3204,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "n.741C>A",
"hgvs_p": null,
"transcript": "ENST00000369073.3",
"protein_id": null,
"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": 1135,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "n.635C>A",
"hgvs_p": null,
"transcript": "NR_134516.1",
"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": 1042,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.*64C>A",
"hgvs_p": null,
"transcript": "NM_001318166.2",
"protein_id": "NP_001305095.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 193,
"cds_start": -4,
"cds_end": null,
"cds_length": 582,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3333,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.*200C>A",
"hgvs_p": null,
"transcript": "NM_001318168.2",
"protein_id": "NP_001305097.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 96,
"cds_start": -4,
"cds_end": null,
"cds_length": 291,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3178,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"hgvs_c": "c.*29C>A",
"hgvs_p": null,
"transcript": "NM_001318169.2",
"protein_id": "NP_001305098.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 96,
"cds_start": -4,
"cds_end": null,
"cds_length": 291,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3007,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PLPP4",
"gene_hgnc_id": 23531,
"dbsnp": "rs1047369",
"frequency_reference_population": 6.840675e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.84068e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.08009609580039978,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.029,
"revel_prediction": "Benign",
"alphamissense_score": 0.1432,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.54,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.026,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000398250.6",
"gene_symbol": "PLPP4",
"hgnc_id": 23531,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.771C>A",
"hgvs_p": "p.Ser257Arg"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}