The UMD-MSH2 mutations database
Record ID: 426

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1689T>Gp.Tyr563X

wt codonwt aamutant codonmutant aamutational eventmutation type
TATTyrTAGStopT->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization NoNo

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_44620_83274_08-397321EGRelative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data