The UMD-MSH2 mutations database
Record ID: 1648

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.803delCp.Ser268TyrfsX6

wt codonwt aamutant codonmutant aamutational eventmutation type
TCASerdel1bFs.Stop at 273Fr.

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
7_4353 (04K223)2478E04060Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data