The UMD-MSH2 mutations database
Record ID: 2608

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.847delGp.Asp283IlefsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
GATAspdel1aFs.Stop at 291Fr.

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_-4487---G06643Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data