← 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: 10-119933734-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=119933734&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 119933734,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000369075.8",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "c.2970A>G",
"hgvs_p": "p.Thr990Thr",
"transcript": "NM_007190.4",
"protein_id": "NP_009121.1",
"transcript_support_level": null,
"aa_start": 990,
"aa_end": null,
"aa_length": 1000,
"cds_start": 2970,
"cds_end": null,
"cds_length": 3003,
"cdna_start": 3023,
"cdna_end": null,
"cdna_length": 7148,
"mane_select": "ENST00000369075.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "c.2970A>G",
"hgvs_p": "p.Thr990Thr",
"transcript": "ENST00000369075.8",
"protein_id": "ENSP00000358071.3",
"transcript_support_level": 1,
"aa_start": 990,
"aa_end": null,
"aa_length": 1000,
"cds_start": 2970,
"cds_end": null,
"cds_length": 3003,
"cdna_start": 3023,
"cdna_end": null,
"cdna_length": 7148,
"mane_select": "NM_007190.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "c.2967A>G",
"hgvs_p": "p.Thr989Thr",
"transcript": "NM_001411070.1",
"protein_id": "NP_001397999.1",
"transcript_support_level": null,
"aa_start": 989,
"aa_end": null,
"aa_length": 999,
"cds_start": 2967,
"cds_end": null,
"cds_length": 3000,
"cdna_start": 3020,
"cdna_end": null,
"cdna_length": 7145,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "c.2967A>G",
"hgvs_p": "p.Thr989Thr",
"transcript": "ENST00000705471.1",
"protein_id": "ENSP00000516127.1",
"transcript_support_level": null,
"aa_start": 989,
"aa_end": null,
"aa_length": 999,
"cds_start": 2967,
"cds_end": null,
"cds_length": 3000,
"cdna_start": 3043,
"cdna_end": null,
"cdna_length": 4613,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "c.2970A>G",
"hgvs_p": "p.Thr990Thr",
"transcript": "XM_047424537.1",
"protein_id": "XP_047280493.1",
"transcript_support_level": null,
"aa_start": 990,
"aa_end": null,
"aa_length": 1000,
"cds_start": 2970,
"cds_end": null,
"cds_length": 3003,
"cdna_start": 3023,
"cdna_end": null,
"cdna_length": 3127,
"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": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "n.516A>G",
"hgvs_p": null,
"transcript": "ENST00000475542.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 552,
"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": 17,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "n.2490A>G",
"hgvs_p": null,
"transcript": "NR_037771.2",
"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": 6615,
"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": 18,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "n.3020A>G",
"hgvs_p": null,
"transcript": "XR_007061940.1",
"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": 4315,
"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": 18,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"hgvs_c": "n.3023A>G",
"hgvs_p": null,
"transcript": "XR_246061.3",
"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": 4318,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "SEC23IP",
"gene_hgnc_id": 17018,
"dbsnp": "rs34826964",
"frequency_reference_population": 0.06746383,
"hom_count_reference_population": 6289,
"allele_count_reference_population": 107565,
"gnomad_exomes_af": 0.0688082,
"gnomad_genomes_af": 0.0547325,
"gnomad_exomes_ac": 99230,
"gnomad_genomes_ac": 8335,
"gnomad_exomes_homalt": 5857,
"gnomad_genomes_homalt": 432,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.550000011920929,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.55,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.549,
"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": -14,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6,BP7,BA1",
"acmg_by_gene": [
{
"score": -14,
"benign_score": 14,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6",
"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000369075.8",
"gene_symbol": "SEC23IP",
"hgnc_id": 17018,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2970A>G",
"hgvs_p": "p.Thr990Thr"
}
],
"clinvar_disease": "SEC23IP-related disorder",
"clinvar_classification": "Benign",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "SEC23IP-related disorder",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}