Annotation Detail
Information
- Associated Genes
- MSH3
- Associated Variants
-
MSH3 p.Ala1045Thr (p.A1045T)
(
ENST00000265081.7,
ENST00000658259.1,
ENST00000667069.1 )
MSH3 p.Ala1045Thr (p.A1045T) ( ENST00000265081.7, ENST00000658259.1, ENST00000667069.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002439.5(MSH3):c.3133G>A (p.Ala1045Thr) AND not provided
- ClinVar Allele ID
- 808716
- ClinVar RefSeq Alternation Syntax
- NM_002439.5:c.3133G>A
- 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/RCV001520312
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs