The UMD-MSH2 mutations database
Record ID: 3137

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2254delAp.Arg752GlufsX11

wt codonwt aamutant codonmutant aamutational eventmutation type
AGAArgdel1aFs.Stop at 762Fr.

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
31_H1426H1426-5H1426-5ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data