Annotation Detail
Information
- Associated Genes
- PIK3CA
- Associated Variants
-
PIK3CA p.Gly118Asp (p.G118D)
(
ENST00000263967.4,
ENST00000643187.1 )
PIK3CA p.Gly118Asp (p.G118D) ( ENST00000263967.4, ENST00000643187.1 ) - Associated Disease
- Cowden syndrome
- Source Database
- ClinVar
- Description
- NM_006218.4(PIK3CA):c.353G>A (p.Gly118Asp) AND Cowden syndrome
- ClinVar Allele ID
- 166218
- ClinVar RefSeq Alternation Syntax
- NM_006218.4:c.353G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-06-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002512561
- ClinVar Disease
- Cowden syndrome
- Observed Origin Sample
- germline
Drugs