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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: 19-18219036-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=18219036&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 18219036,
"ref": "C",
"alt": "T",
"effect": "splice_region_variant,synonymous_variant",
"transcript": "ENST00000262805.17",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.873G>A",
"hgvs_p": "p.Glu291Glu",
"transcript": "NM_001098818.4",
"protein_id": "NP_001092288.1",
"transcript_support_level": null,
"aa_start": 291,
"aa_end": null,
"aa_length": 680,
"cds_start": 873,
"cds_end": null,
"cds_length": 2043,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 5030,
"mane_select": "ENST00000262805.17",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.873G>A",
"hgvs_p": "p.Glu291Glu",
"transcript": "ENST00000262805.17",
"protein_id": "ENSP00000262805.10",
"transcript_support_level": 1,
"aa_start": 291,
"aa_end": null,
"aa_length": 680,
"cds_start": 873,
"cds_end": null,
"cds_length": 2043,
"cdna_start": 896,
"cdna_end": null,
"cdna_length": 5030,
"mane_select": "NM_001098818.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": null,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "ENST00000355502.7",
"protein_id": "ENSP00000347689.2",
"transcript_support_level": 2,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1841,
"cdna_end": null,
"cdna_length": 5979,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "ENST00000594465.7",
"protein_id": "ENSP00000470210.1",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1449,
"cdna_end": null,
"cdna_length": 2988,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "ENST00000594617.7",
"protein_id": "ENSP00000469696.1",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1208,
"cdna_end": null,
"cdna_length": 4655,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.651G>A",
"hgvs_p": "p.Glu217Glu",
"transcript": "ENST00000447275.7",
"protein_id": "ENSP00000402091.1",
"transcript_support_level": 1,
"aa_start": 217,
"aa_end": null,
"aa_length": 606,
"cds_start": 651,
"cds_end": null,
"cds_length": 1821,
"cdna_start": 986,
"cdna_end": null,
"cdna_length": 2542,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.276G>A",
"hgvs_p": "p.Glu92Glu",
"transcript": "ENST00000539010.5",
"protein_id": "ENSP00000439470.1",
"transcript_support_level": 1,
"aa_start": 92,
"aa_end": null,
"aa_length": 481,
"cds_start": 276,
"cds_end": null,
"cds_length": 1446,
"cdna_start": 431,
"cdna_end": null,
"cdna_length": 1699,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.389G>A",
"hgvs_p": null,
"transcript": "ENST00000597297.1",
"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": 1559,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.*245G>A",
"hgvs_p": null,
"transcript": "ENST00000598111.7",
"protein_id": "ENSP00000474591.4",
"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": 1284,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.*245G>A",
"hgvs_p": null,
"transcript": "ENST00000598111.7",
"protein_id": "ENSP00000474591.4",
"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": 1284,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "NM_000923.6",
"protein_id": "NP_000914.2",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1208,
"cdna_end": null,
"cdna_length": 5342,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "NM_001330172.2",
"protein_id": "NP_001317101.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1207,
"cdna_end": null,
"cdna_length": 5341,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.969G>A",
"hgvs_p": "p.Glu323Glu",
"transcript": "NM_001414480.1",
"protein_id": "NP_001401409.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 712,
"cds_start": 969,
"cds_end": null,
"cds_length": 2139,
"cdna_start": 1784,
"cdna_end": null,
"cdna_length": 5918,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.651G>A",
"hgvs_p": "p.Glu217Glu",
"transcript": "NM_001098819.4",
"protein_id": "NP_001092289.1",
"transcript_support_level": null,
"aa_start": 217,
"aa_end": null,
"aa_length": 606,
"cds_start": 651,
"cds_end": null,
"cds_length": 1821,
"cdna_start": 986,
"cdna_end": null,
"cdna_length": 5120,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.651G>A",
"hgvs_p": "p.Glu217Glu",
"transcript": "NM_001395274.1",
"protein_id": "NP_001382203.1",
"transcript_support_level": null,
"aa_start": 217,
"aa_end": null,
"aa_length": 606,
"cds_start": 651,
"cds_end": null,
"cds_length": 1821,
"cdna_start": 1640,
"cdna_end": null,
"cdna_length": 5774,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"splice_region_variant",
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "c.276G>A",
"hgvs_p": "p.Glu92Glu",
"transcript": "NM_001369701.2",
"protein_id": "NP_001356630.1",
"transcript_support_level": null,
"aa_start": 92,
"aa_end": null,
"aa_length": 481,
"cds_start": 276,
"cds_end": null,
"cds_length": 1446,
"cdna_start": 846,
"cdna_end": null,
"cdna_length": 4980,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.1964G>A",
"hgvs_p": null,
"transcript": "ENST00000597360.5",
"protein_id": null,
"transcript_support_level": 2,
"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": 3511,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"splice_region_variant",
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.*127G>A",
"hgvs_p": null,
"transcript": "ENST00000599188.5",
"protein_id": "ENSP00000473713.2",
"transcript_support_level": 5,
"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": 2101,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"hgvs_c": "n.*127G>A",
"hgvs_p": null,
"transcript": "ENST00000599188.5",
"protein_id": "ENSP00000473713.2",
"transcript_support_level": 5,
"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": 2101,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "ENSG00000268650",
"gene_hgnc_id": null,
"hgvs_c": "n.571-473C>T",
"hgvs_p": null,
"transcript": "ENST00000594805.3",
"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": 855,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "PDE4C",
"gene_hgnc_id": 8782,
"dbsnp": "rs3179757",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.5,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0.03999999910593033,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.5,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.672,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.04,
"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": -3,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Strong,BP7",
"acmg_by_gene": [
{
"score": -3,
"benign_score": 5,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000262805.17",
"gene_symbol": "PDE4C",
"hgnc_id": 8782,
"effects": [
"splice_region_variant",
"synonymous_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.873G>A",
"hgvs_p": "p.Glu291Glu"
},
{
"score": -2,
"benign_score": 4,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000594805.3",
"gene_symbol": "ENSG00000268650",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.571-473C>T",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}