The UMD-MSH2 mutations database
Record ID: 907

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1963G>Ap.Val655Ile

wt codonwt aamutant codonmutant aamutational eventmutation type
GTAValATAIleG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 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)
10.29 (non pathogenous)23 (Polymorphism)

Patient and sample data


Sample IDPatient status
20_20-1246_1246-72_---Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data