The UMD-MSH2 mutations database
Record ID: 3177

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.790C>Tp.Gln264X

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
4_JCS1312309434600Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data