The UMD-MSH2 mutations database
Record ID: 278

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS10-18T>C (c.1662-18T>C)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerspl-18Spl.T>C

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

Impact on splicing
Splice site type Wild type sequence CV Mutant type sequence CV Variation (%)

Patient and sample data


Sample IDPatient status
5_2011438_20113682_AAF518Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data