Annotation Detail
Information
- Associated Genes
- PTGS2
- Associated Variants
-
PTGS2 c.*427T>C
(
ENST00000680451.1,
ENST00000367468.10 )
PTGS2 c.*427T>C ( ENST00000367468.10, ENST00000680451.1 ) - Source Database
- ClinVar
- Description
- NM_000963.4(PTGS2):c.*427T>C AND Cholangiocarcinoma
- ClinVar Allele ID
- 2736345
- ClinVar RefSeq Alternation Syntax
- NM_000963.4:c.*427T>C
- Clinical Significance Description
- other
- Clinical Significance Last Update
- 2022-12-10
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003312793
- Observed Origin Sample
- germline
Drugs