The UMD-MSH2 mutations database
Record ID: 793

Mutation description


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

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

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 _
catgtgtttaagCA
72.9 _ *
-11.4 %

Patient and sample data


Sample IDPatient status
19_531_531-001_531-001-1Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data