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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: 3-122284209-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=122284209&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 122284209,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000639785.2",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "NM_000388.4",
"protein_id": "NP_000379.3",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 2642,
"cdna_end": null,
"cdna_length": 10062,
"mane_select": "ENST00000639785.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "ENST00000639785.2",
"protein_id": "ENSP00000491584.2",
"transcript_support_level": 1,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 2642,
"cdna_end": null,
"cdna_length": 10062,
"mane_select": "NM_000388.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2285G>A",
"hgvs_p": "p.Arg762His",
"transcript": "ENST00000498619.4",
"protein_id": "ENSP00000420194.1",
"transcript_support_level": 1,
"aa_start": 762,
"aa_end": null,
"aa_length": 1088,
"cds_start": 2285,
"cds_end": null,
"cds_length": 3267,
"cdna_start": 2723,
"cdna_end": null,
"cdna_length": 5009,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2285G>A",
"hgvs_p": "p.Arg762His",
"transcript": "NM_001178065.2",
"protein_id": "NP_001171536.2",
"transcript_support_level": null,
"aa_start": 762,
"aa_end": null,
"aa_length": 1088,
"cds_start": 2285,
"cds_end": null,
"cds_length": 3267,
"cdna_start": 2730,
"cdna_end": null,
"cdna_length": 10150,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "ENST00000638421.1",
"protein_id": "ENSP00000492190.1",
"transcript_support_level": 5,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 2794,
"cdna_end": null,
"cdna_length": 5088,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2024G>A",
"hgvs_p": "p.Arg675His",
"transcript": "ENST00000490131.7",
"protein_id": "ENSP00000418685.2",
"transcript_support_level": 5,
"aa_start": 675,
"aa_end": null,
"aa_length": 1001,
"cds_start": 2024,
"cds_end": null,
"cds_length": 3006,
"cdna_start": 2266,
"cdna_end": null,
"cdna_length": 4015,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "XM_006713789.4",
"protein_id": "XP_006713852.1",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 2700,
"cdna_end": null,
"cdna_length": 10120,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "XM_017007324.2",
"protein_id": "XP_016862813.1",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 4574,
"cdna_end": null,
"cdna_length": 11994,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His",
"transcript": "XM_017007325.2",
"protein_id": "XP_016862814.1",
"transcript_support_level": null,
"aa_start": 752,
"aa_end": null,
"aa_length": 1078,
"cds_start": 2255,
"cds_end": null,
"cds_length": 3237,
"cdna_start": 2599,
"cdna_end": null,
"cdna_length": 10019,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "H",
"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": "CASR",
"gene_hgnc_id": 1514,
"hgvs_c": "c.1772G>A",
"hgvs_p": "p.Arg591His",
"transcript": "XM_047449065.1",
"protein_id": "XP_047305021.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 917,
"cds_start": 1772,
"cds_end": null,
"cds_length": 2754,
"cdna_start": 2393,
"cdna_end": null,
"cdna_length": 9813,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "CASR",
"gene_hgnc_id": 1514,
"dbsnp": "rs771529256",
"frequency_reference_population": 0.00001301233,
"hom_count_reference_population": 0,
"allele_count_reference_population": 21,
"gnomad_exomes_af": 0.0000129987,
"gnomad_genomes_af": 0.0000131432,
"gnomad_exomes_ac": 19,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.5552722215652466,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.616,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.1173,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.01,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 2.539,
"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": "PM1,PM5,PP2,BP6",
"acmg_by_gene": [
{
"score": 4,
"benign_score": 1,
"pathogenic_score": 5,
"criteria": [
"PM1",
"PM5",
"PP2",
"BP6"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000639785.2",
"gene_symbol": "CASR",
"hgnc_id": 1514,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR,AD",
"hgvs_c": "c.2255G>A",
"hgvs_p": "p.Arg752His"
}
],
"clinvar_disease": " 8, idiopathic generalized, susceptibility to,Autosomal dominant hypocalcemia 1,Epilepsy,Familial hypocalciuric hypercalcemia,Familial hypocalciuric hypercalcemia 1,Familial hypoparathyroidism,Neonatal severe primary hyperparathyroidism,Nephrolithiasis/nephrocalcinosis",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "US:5 LB:2",
"phenotype_combined": "Familial hypocalciuric hypercalcemia;Autosomal dominant hypocalcemia 1|Familial hypocalciuric hypercalcemia 1|Neonatal severe primary hyperparathyroidism|Familial hypoparathyroidism|Neonatal severe primary hyperparathyroidism;Familial hypocalciuric hypercalcemia 1;Autosomal dominant hypocalcemia 1;Epilepsy, idiopathic generalized, susceptibility to, 8|Autosomal dominant hypocalcemia 1|Nephrolithiasis/nephrocalcinosis",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}