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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: 9-35740225-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=35740225&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 35740225,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000378103.7",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "NM_020944.3",
"protein_id": "NP_065995.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 927,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2784,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 3611,
"mane_select": "ENST00000378103.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "ENST00000378103.7",
"protein_id": "ENSP00000367343.3",
"transcript_support_level": 1,
"aa_start": 423,
"aa_end": null,
"aa_length": 927,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2784,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 3611,
"mane_select": "NM_020944.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "ENST00000378094.4",
"protein_id": "ENSP00000367334.4",
"transcript_support_level": 1,
"aa_start": 423,
"aa_end": null,
"aa_length": 877,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2634,
"cdna_start": 1781,
"cdna_end": null,
"cdna_length": 3757,
"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": 4,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "n.839G>A",
"hgvs_p": null,
"transcript": "ENST00000467252.5",
"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": 1913,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "NM_001330660.2",
"protein_id": "NP_001317589.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 877,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2634,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 3768,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Gly429Ser",
"transcript": "XM_006716809.5",
"protein_id": "XP_006716872.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 933,
"cds_start": 1285,
"cds_end": null,
"cds_length": 2802,
"cdna_start": 1809,
"cdna_end": null,
"cdna_length": 3629,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Gly429Ser",
"transcript": "XM_005251526.6",
"protein_id": "XP_005251583.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 911,
"cds_start": 1285,
"cds_end": null,
"cds_length": 2736,
"cdna_start": 1809,
"cdna_end": null,
"cdna_length": 3563,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "XM_017014937.3",
"protein_id": "XP_016870426.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 905,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2718,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 3545,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1285G>A",
"hgvs_p": "p.Gly429Ser",
"transcript": "XM_017014938.3",
"protein_id": "XP_016870427.1",
"transcript_support_level": null,
"aa_start": 429,
"aa_end": null,
"aa_length": 883,
"cds_start": 1285,
"cds_end": null,
"cds_length": 2652,
"cdna_start": 1809,
"cdna_end": null,
"cdna_length": 3786,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser",
"transcript": "XM_017014939.3",
"protein_id": "XP_016870428.1",
"transcript_support_level": null,
"aa_start": 423,
"aa_end": null,
"aa_length": 855,
"cds_start": 1267,
"cds_end": null,
"cds_length": 2568,
"cdna_start": 1791,
"cdna_end": null,
"cdna_length": 3702,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1048G>A",
"hgvs_p": "p.Gly350Ser",
"transcript": "XM_017014940.3",
"protein_id": "XP_016870429.1",
"transcript_support_level": null,
"aa_start": 350,
"aa_end": null,
"aa_length": 854,
"cds_start": 1048,
"cds_end": null,
"cds_length": 2565,
"cdna_start": 1572,
"cdna_end": null,
"cdna_length": 3392,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.1048G>A",
"hgvs_p": "p.Gly350Ser",
"transcript": "XM_017014941.3",
"protein_id": "XP_016870430.1",
"transcript_support_level": null,
"aa_start": 350,
"aa_end": null,
"aa_length": 804,
"cds_start": 1048,
"cds_end": null,
"cds_length": 2415,
"cdna_start": 1572,
"cdna_end": null,
"cdna_length": 3549,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.832G>A",
"hgvs_p": "p.Gly278Ser",
"transcript": "XM_017014942.3",
"protein_id": "XP_016870431.1",
"transcript_support_level": null,
"aa_start": 278,
"aa_end": null,
"aa_length": 782,
"cds_start": 832,
"cds_end": null,
"cds_length": 2349,
"cdna_start": 923,
"cdna_end": null,
"cdna_length": 2743,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.814G>A",
"hgvs_p": "p.Gly272Ser",
"transcript": "XM_017014943.3",
"protein_id": "XP_016870432.1",
"transcript_support_level": null,
"aa_start": 272,
"aa_end": null,
"aa_length": 776,
"cds_start": 814,
"cds_end": null,
"cds_length": 2331,
"cdna_start": 905,
"cdna_end": null,
"cdna_length": 2725,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.730G>A",
"hgvs_p": "p.Gly244Ser",
"transcript": "XM_017014944.1",
"protein_id": "XP_016870433.1",
"transcript_support_level": null,
"aa_start": 244,
"aa_end": null,
"aa_length": 748,
"cds_start": 730,
"cds_end": null,
"cds_length": 2247,
"cdna_start": 854,
"cdna_end": null,
"cdna_length": 2674,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.712G>A",
"hgvs_p": "p.Gly238Ser",
"transcript": "XM_017014945.1",
"protein_id": "XP_016870434.1",
"transcript_support_level": null,
"aa_start": 238,
"aa_end": null,
"aa_length": 742,
"cds_start": 712,
"cds_end": null,
"cds_length": 2229,
"cdna_start": 836,
"cdna_end": null,
"cdna_length": 2656,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"hgvs_c": "c.712G>A",
"hgvs_p": "p.Gly238Ser",
"transcript": "XM_047423612.1",
"protein_id": "XP_047279568.1",
"transcript_support_level": null,
"aa_start": 238,
"aa_end": null,
"aa_length": 742,
"cds_start": 712,
"cds_end": null,
"cds_length": 2229,
"cdna_start": 934,
"cdna_end": null,
"cdna_length": 2754,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "GBA2",
"gene_hgnc_id": 18986,
"dbsnp": "rs79325774",
"frequency_reference_population": 0.0024013233,
"hom_count_reference_population": 79,
"allele_count_reference_population": 3876,
"gnomad_exomes_af": 0.00128946,
"gnomad_genomes_af": 0.0130768,
"gnomad_exomes_ac": 1885,
"gnomad_genomes_ac": 1991,
"gnomad_exomes_homalt": 35,
"gnomad_genomes_homalt": 44,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.002217531204223633,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.051,
"revel_prediction": "Benign",
"alphamissense_score": 0.0796,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.51,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.729,
"phylop100way_prediction": "Uncertain_significance",
"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": "ENST00000378103.7",
"gene_symbol": "GBA2",
"hgnc_id": 18986,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1267G>A",
"hgvs_p": "p.Gly423Ser"
}
],
"clinvar_disease": "Hereditary spastic paraplegia,Spastic paraplegia,not provided,not specified",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:5",
"phenotype_combined": "not provided|Spastic paraplegia|not specified|Hereditary spastic paraplegia",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}