The UMD-MSH2 mutations database
Record ID: 318

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2432dupp.Leu811PhefsX13

wt codonwt aamutant codonmutant aamutational eventmutation type
TTALeuins1cFs.Stop at 823

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

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_2005110_20052068_AAA723Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data