The UMD-MSH2 mutations database
Record ID: 316

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS13-1G>A (c.2211-1G>A)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGGArgspl-1Spl.G>A

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

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
tatgtgcttcagGT
89.1 _
tatgtgcttcaaGT
60.1 _ *
-32.5 %

Patient and sample data


Sample IDPatient status
5_2010454_20100088_AAE470Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data