The UMD-MSH2 mutations database
Record ID: 377

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS15-3C>T (c.2635-3C>T)

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnspl-3Spl.C>T

StructureKey Residue (HCD)Pyrimidin doubletCpG
MSH3/MSH6 interaction 

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
catgtgtttcagCA
82.3 _
catgtgttttagCA
74.6 _
-9.3 %

Patient and sample data


Sample IDPatient status
6_601146_20063661_S7476Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data