The UMD-MSH2 mutations database
Record ID: 3048

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.835C>Gp.Leu279Val

wt codonwt aamutant codonmutant aamutational eventmutation type
CTCLeuGTCValC->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 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)
0.990.31 (non pathogenous)29 (Polymorphism)

Patient and sample data


Sample IDPatient status
19_2425324253-00124253-001Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data