Annotation Detail
Information
- Associated Genes
- MSH2
- Associated Variants
-
MSH2 p.Arg389Ter (p.R389*)
(
ENST00000233146.7,
ENST00000406134.5,
ENST00000543555.6,
ENST00000645506.1,
ENST00000713854.1,
ENST00000713860.1,
ENST00000713861.1,
ENST00000713919.1 )
MSH2 p.Arg389Ter (p.R389*) ( ENST00000233146.7, ENST00000406134.5, ENST00000543555.6, ENST00000645506.1, ENST00000713854.1, ENST00000713860.1, ENST00000713861.1, ENST00000713919.1 ) - Associated Disease
- Hereditary nonpolyposis colorectal neoplasms
- Source Database
- ClinVar
- Description
- NM_000251.3(MSH2):c.1165C>T (p.Arg389Ter) AND Hereditary nonpolyposis colorectal neoplasms
- ClinVar Allele ID
- 96032
- ClinVar RefSeq Alternation Syntax
- NM_001258281.1:c.967C>T
- ClinVar RefSeq Alternation Syntax
- NM_000251.3:c.1165C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000524332
- ClinVar Disease
- Hereditary nonpolyposis colorectal neoplasms
- Observed Origin Sample
- germline
Drugs