The UMD-MSH2 mutations database
Record ID: 976

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.163delCp.Arg55GlyfsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
CGGArgdel1aFs.Stop at 63Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 

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_H10_H10_1_H10_1_ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data