The UMD-MSH2 mutations database
Record ID: 2394

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.332_333insCCp.Ser112HisfsX63

wt codonwt aamutant codonmutant aamutational eventmutation type
GCAAlains2cFs.Stop at 174

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 

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
SO_-881---G01555Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data