The UMD-MSH2 mutations database
Record ID: 1441

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1255C>Tp.Gln419X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlnTAGStopC->TTs

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
7_-1011C010121Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data