The UMD-MSH2 mutations database
Record ID: 286

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1699A>Tp.Lys567X

wt codonwt aamutant codonmutant aamutational eventmutation type
AAALysTAAStopA->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 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
5_1998009_20032925_AAA990Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data