Annotation Detail
Information
- Associated Genes
- WRN
- Associated Variants
-
WRN p.Leu1074Phe (p.L1074F)
(
ENST00000298139.7 )
WRN p.Leu1074Phe (p.L1074F) ( ENST00000298139.7 ) - Associated Disease
- Werner syndrome
- Source Database
- ClinVar
- Description
- NM_000553.6(WRN):c.3222G>T (p.Leu1074Phe) AND Werner syndrome
- ClinVar Allele ID
- 136205
- ClinVar RefSeq Alternation Syntax
- NM_000553.6:c.3222G>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-02-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000281792
- ClinVar Disease
- Werner syndrome
- Observed Origin Sample
- germline
Drugs