The UMD-MSH2 mutations database
Record ID: 2033

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.592G>Tp.Glu198X

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluTAAStopG->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector Yes, non coding strandNo

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_-6065---E051239Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data