The UMD-MSH2 mutations database
Record ID: 857

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.793_1076delp.Val265IlefsX29

wt codonwt aamutant codonmutant aamutational eventmutation type
GTTValdel284aFs.Stop at 293Fr.

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
19_15755_15755-004_15755-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data