The UMD-MSH2 mutations database
Record ID: 1352

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.943_1076delp.Gly315IlefsX29

wt codonwt aamutant codonmutant aamutational eventmutation type
GGTGlydel134aFs.Stop at 343Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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
37_L11.083_20239_131455Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data