Annotation Detail
Information
- Associated Genes
- MSH2
- Associated Variants
-
MSH2 p.Ala2Thr (p.A2T)
(
ENST00000233146.7,
ENST00000406134.5,
ENST00000543555.6,
ENST00000645506.1,
ENST00000713854.1,
ENST00000713860.1,
ENST00000713861.1,
ENST00000713919.1 )
MSH2 p.Ala2Thr (p.A2T) ( 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.4G>A (p.Ala2Thr) AND Hereditary nonpolyposis colorectal neoplasms
- ClinVar Allele ID
- 50089
- ClinVar RefSeq Alternation Syntax
- NM_001258281.1:c.-31+20G>A
- ClinVar RefSeq Alternation Syntax
- NM_000251.3:c.4G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001083980
- ClinVar Disease
- Hereditary nonpolyposis colorectal neoplasms
- Observed Origin Sample
- germline
Drugs