The UMD-MSH2 mutations database
Record ID: 2459

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.793_942delp.Val265_Gln314del

wt codonwt aamutant codonmutant aamutational eventmutation type
GTTValdel150aInFIn frame delInF

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
SO_-2526---G03192Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data