The UMD-MSH2 mutations database
Record ID: 442

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2442T>Cp.Leu814Leu

wt codonwt aamutant codonmutant aamutational eventmutation type
CTTLeuCTCLeuT->CTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase Yes, coding strandNo

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)
11.00 (non pathogenous)18 (Polymorphism)

Patient and sample data


Sample IDPatient status
8_44224_78075_08-797021EGRelative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data