The UMD-MSH2 mutations database
Record ID: 2959

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.792delGp.Val265LeufsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlndel1cFs.Stop at 273Fr.

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
31_H1289H1289-1H1289-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data