The UMD-MSH2 mutations database
Record ID: 1223

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1861C>Tp.Arg621X

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgTGAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase NoYes

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
37_F07.158_6574_62642Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data