The UMD-MSH2 mutations database
Record ID: 2673

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS7-10T>C (c.1277-10T>C)

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlyspl-10Spl.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 (%)
Acceptor
actttcttttagGA
84.4 _
accttcttttagGA
83.7 _
-0.8 %

Patient and sample data


Sample IDPatient status
SO_-5037---G07710Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data