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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: 11-111737534-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=111737534&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 111737534,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_181699.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "ENST00000311129.9",
"protein_id": "ENSP00000311344.5",
"transcript_support_level": 1,
"aa_start": 609,
"aa_end": null,
"aa_length": 667,
"cds_start": 1825,
"cds_end": null,
"cds_length": 2004,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000311129.9"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "NM_181699.3",
"protein_id": "NP_859050.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 667,
"cds_start": 1825,
"cds_end": null,
"cds_length": 2004,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_181699.3"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1633G>A",
"hgvs_p": "p.Val545Met",
"transcript": "NM_181700.2",
"protein_id": "NP_859051.1",
"transcript_support_level": null,
"aa_start": 545,
"aa_end": null,
"aa_length": 603,
"cds_start": 1633,
"cds_end": null,
"cds_length": 1812,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_181700.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1633G>A",
"hgvs_p": "p.Val545Met",
"transcript": "ENST00000426998.6",
"protein_id": "ENSP00000410671.2",
"transcript_support_level": 2,
"aa_start": 545,
"aa_end": null,
"aa_length": 603,
"cds_start": 1633,
"cds_end": null,
"cds_length": 1812,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000426998.6"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427196.1",
"protein_id": "XP_047283152.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 688,
"cds_start": 1825,
"cds_end": null,
"cds_length": 2067,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427196.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427189.1",
"protein_id": "XP_047283145.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 661,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1986,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427189.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427190.1",
"protein_id": "XP_047283146.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 661,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1986,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427190.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427191.1",
"protein_id": "XP_047283147.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 661,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1986,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427191.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427192.1",
"protein_id": "XP_047283148.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 661,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1986,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427192.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427193.1",
"protein_id": "XP_047283149.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 640,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1923,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427193.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427194.1",
"protein_id": "XP_047283150.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 640,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1923,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427194.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met",
"transcript": "XM_047427195.1",
"protein_id": "XP_047283151.1",
"transcript_support_level": null,
"aa_start": 609,
"aa_end": null,
"aa_length": 640,
"cds_start": 1825,
"cds_end": null,
"cds_length": 1923,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047427195.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1690G>A",
"hgvs_p": "p.Val564Met",
"transcript": "XM_017017960.2",
"protein_id": "XP_016873449.1",
"transcript_support_level": null,
"aa_start": 564,
"aa_end": null,
"aa_length": 622,
"cds_start": 1690,
"cds_end": null,
"cds_length": 1869,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017017960.2"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "c.1690G>A",
"hgvs_p": "p.Val564Met",
"transcript": "XM_024448600.2",
"protein_id": "XP_024304368.1",
"transcript_support_level": null,
"aa_start": 564,
"aa_end": null,
"aa_length": 595,
"cds_start": 1690,
"cds_end": null,
"cds_length": 1788,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024448600.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"hgvs_c": "n.-31G>A",
"hgvs_p": null,
"transcript": "ENST00000526287.1",
"protein_id": null,
"transcript_support_level": 1,
"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": "ENST00000526287.1"
}
],
"gene_symbol": "PPP2R1B",
"gene_hgnc_id": 9303,
"dbsnp": "rs45568137",
"frequency_reference_population": 0.0000013680939,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000136809,
"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": 0.16678380966186523,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.031,
"revel_prediction": "Benign",
"alphamissense_score": 0.0986,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.54,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.088,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.03,
"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": "NM_181699.3",
"gene_symbol": "PPP2R1B",
"hgnc_id": 9303,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1825G>A",
"hgvs_p": "p.Val609Met"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}