The UMD-MSH2 mutations database
Record ID: 636

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1186A>Tp.Arg396X

wt codonwt aamutant codonmutant aamutational eventmutation type
AGAArgTGAStopA->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization Yes, non 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
19_13174_13174-001_13174-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data