The UMD-MSH2 mutations database
Record ID: 899

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1147C>Tp.Arg383X

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgTGAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization Yes, coding strandYes

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Patient and sample data


Sample IDPatient status
20_20-1509_1509-01_4835Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data