The UMD-MSH2 mutations database
Record ID: 2108

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.339G>Ap.Lys113Lys

wt codonwt aamutant codonmutant aamutational eventmutation type
AAGLysAAALysG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding Yes, non 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)
0.651.00 (non pathogenous)18 (Polymorphism)

Patient and sample data


Sample IDPatient status
7_5389 (05K267)4961E06010Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data