The UMD-MSH2 mutations database
Record ID: 1041

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.734T>Gp.Leu245Trp

wt codonwt aamutant codonmutant aamutational eventmutation type
TTGLeuTGGTrpT->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 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)
0.990.00 (pathogenous)82 (Pathogenous)

Patient and sample data


Sample IDPatient status
31_H743_H743-1_H743-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data