The UMD-MSH2 mutations database
Record ID: 388

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.940C>Tp.Gln314X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlnTAGStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization Yes, coding strandNo

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
6_606216_200604864_S6620Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data