The UMD-MSH2 mutations database
Record ID: 1887

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2131C>Tp.Arg711X

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgTGAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 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
7_-36903927E050548Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data