The UMD-MSH2 mutations database
Record ID: 477

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1221_1222delCTp.Tyr408SerfsX8

wt codonwt aamutant codonmutant aamutational eventmutation type
CTCLeudel2cFs.Stop at 415Fr.

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
14_F0785_04C510_04C510Relative

Clinical data


Symptom

Reference


Reference IDReference
14Unpublished data