The UMD-MSH2 mutations database
Record ID: 418

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1571G>Ap.Arg524His

wt codonwt aamutant codonmutant aamutational eventmutation type
CGTArgCATHisG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization NoYes

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
10.00 (pathogenous)71 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
8_35760_9111941_08-242160Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data