The UMD-MSH2 mutations database
Record ID: 269

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1413dupp.Pro472ThrfsX4

wt codonwt aamutant codonmutant aamutational eventmutation type
CCTProins1aFs.Stop at 475

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
5_2005009_20060788_AAA808Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data