The UMD-MSH2 mutations database
Record ID: 1691

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS6-43T>G (c.1077-43T>G)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGAArgspl-43Spl.T>G

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
7_-57912947E040799Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data