The UMD-MSH2 mutations database
Record ID: 963

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1216C>Tp.Arg406X

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
31_H92_H92_4_H92_4_ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data