Annotation Detail
Information
- Associated Genes
- PIK3CA
- Associated Variants
-
PIK3CA p.Cys378Tyr (p.C378Y)
(
ENST00000263967.4,
ENST00000643187.1 )
PIK3CA p.Cys378Tyr (p.C378Y) ( ENST00000263967.4, ENST00000643187.1 ) - Associated Disease
- PIK3CA-related disorder
- Source Database
- ClinVar
- Description
- NM_006218.4(PIK3CA):c.1133G>A (p.Cys378Tyr) AND PIK3CA-related disorder
- ClinVar Allele ID
- 48303
- ClinVar RefSeq Alternation Syntax
- NM_006218.4:c.1133G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-08-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004532477
- ClinVar Disease
- PIK3CA-related disorder
- Observed Origin Sample
- germline
Drugs