The UMD-MSH2 mutations database
Record ID: 359

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1418C>Gp.Ser473X

wt codonwt aamutant codonmutant aamutational eventmutation type
TCASerTGAStopC->GTv

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_611261_B00069807_S 2809Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data