The UMD-MSH2 mutations database
Record ID: 435

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2038C>Tp.Arg680X

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgTGAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 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
8_F765_B031444_G1-Nç829Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data