The UMD-MSH2 mutations database
Record ID: 14

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1165C>Tp.Arg389X

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
2_02-DDM4505_23242_23242Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data