The UMD-MSH2 mutations database
Record ID: 2371

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS12-2A>G (c.2006-2A>G)

wt codonwt aamutant codonmutant aamutational eventmutation type
GGCGlyspl-2Spl.A>G

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 

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
tttgttttgtagGC
86.1 _
tttgttttgtggGC
57.1 _ *
-33.6 %

Patient and sample data


Sample IDPatient status
SO_-2229---G01105Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data