The UMD-MSH2 mutations database
Record ID: 1053

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.873_876delGACTp.Thr292LeufsX8

wt codonwt aamutant codonmutant aamutational eventmutation type
CTGLeudel4cFs.Stop at 299Fr.

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_H700_H700-1_H700-1BRelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data