The UMD-MSH2 mutations database
Record ID: 44

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS10-9G>A (c.1662-9G>A)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerspl-9Spl.G>A

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
ttcgatttgcagCA
87 _
ttcaatttgcagCA
86.8 _
-0.1 %

Patient and sample data


Sample IDPatient status
2_02-DDM6993_27261_27261Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data