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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: 1-3414590-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=3414590&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 3414590,
"ref": "C",
"alt": "T",
"effect": "synonymous_variant",
"transcript": "ENST00000270722.10",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro",
"transcript": "NM_022114.4",
"protein_id": "NP_071397.3",
"transcript_support_level": null,
"aa_start": 878,
"aa_end": null,
"aa_length": 1276,
"cds_start": 2634,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 2691,
"cdna_end": null,
"cdna_length": 8698,
"mane_select": "ENST00000270722.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro",
"transcript": "ENST00000270722.10",
"protein_id": "ENSP00000270722.5",
"transcript_support_level": 1,
"aa_start": 878,
"aa_end": null,
"aa_length": 1276,
"cds_start": 2634,
"cds_end": null,
"cds_length": 3831,
"cdna_start": 2691,
"cdna_end": null,
"cdna_length": 8698,
"mane_select": "NM_022114.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro",
"transcript": "ENST00000378391.6",
"protein_id": "ENSP00000367643.2",
"transcript_support_level": 1,
"aa_start": 878,
"aa_end": null,
"aa_length": 1257,
"cds_start": 2634,
"cds_end": null,
"cds_length": 3774,
"cdna_start": 2697,
"cdna_end": null,
"cdna_length": 5447,
"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": 9,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "n.2412C>T",
"hgvs_p": null,
"transcript": "ENST00000512462.5",
"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": 3723,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro",
"transcript": "NM_199454.3",
"protein_id": "NP_955533.2",
"transcript_support_level": null,
"aa_start": 878,
"aa_end": null,
"aa_length": 1257,
"cds_start": 2634,
"cds_end": null,
"cds_length": 3774,
"cdna_start": 2691,
"cdna_end": null,
"cdna_length": 8641,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2637C>T",
"hgvs_p": "p.Pro879Pro",
"transcript": "ENST00000511072.5",
"protein_id": "ENSP00000426975.1",
"transcript_support_level": 5,
"aa_start": 879,
"aa_end": null,
"aa_length": 1178,
"cds_start": 2637,
"cds_end": null,
"cds_length": 3537,
"cdna_start": 2729,
"cdna_end": null,
"cdna_length": 4282,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro",
"transcript": "ENST00000514189.5",
"protein_id": "ENSP00000421400.1",
"transcript_support_level": 5,
"aa_start": 878,
"aa_end": null,
"aa_length": 1177,
"cds_start": 2634,
"cds_end": null,
"cds_length": 3534,
"cdna_start": 2683,
"cdna_end": null,
"cdna_length": 4236,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "P",
"aa_alt": "P",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"hgvs_c": "c.2058C>T",
"hgvs_p": "p.Pro686Pro",
"transcript": "ENST00000509860.1",
"protein_id": "ENSP00000425796.1",
"transcript_support_level": 5,
"aa_start": 686,
"aa_end": null,
"aa_length": 1084,
"cds_start": 2058,
"cds_end": null,
"cds_length": 3255,
"cdna_start": 2058,
"cdna_end": null,
"cdna_length": 3737,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PRDM16",
"gene_hgnc_id": 14000,
"dbsnp": "rs201338158",
"frequency_reference_population": 0.0010338095,
"hom_count_reference_population": 2,
"allele_count_reference_population": 1668,
"gnomad_exomes_af": 0.00107853,
"gnomad_genomes_af": 0.00060446,
"gnomad_exomes_ac": 1576,
"gnomad_genomes_ac": 92,
"gnomad_exomes_homalt": 2,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.47999998927116394,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.009999999776482582,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.48,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.459,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.01,
"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": -17,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS2",
"acmg_by_gene": [
{
"score": -17,
"benign_score": 17,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BP7",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000270722.10",
"gene_symbol": "PRDM16",
"hgnc_id": 14000,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.2634C>T",
"hgvs_p": "p.Pro878Pro"
}
],
"clinvar_disease": "Inborn genetic diseases,Left ventricular noncompaction 8,PRDM16-related disorder,not provided,not specified",
"clinvar_classification": "Benign/Likely benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "LB:4 B:2",
"phenotype_combined": "not specified|Left ventricular noncompaction 8|Inborn genetic diseases|not provided|PRDM16-related disorder",
"pathogenicity_classification_combined": "Benign/Likely benign",
"custom_annotations": null
}
],
"message": null
}