The UMD-MSH2 mutations database
Record ID: 1507

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS15-1G>T (c.2635-1G>T)

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnspl-1Spl.G>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 _
catgtgtttcatCA
53.3 _ *
-35.2 %

Patient and sample data


Sample IDPatient status
7_7631205E02377Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data