The UMD-MSH2 mutations database
Record ID: 2621

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.394dupp.Glu132GlyfsX7

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluins1bFs.Stop at 138

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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_-4080---G06842Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data