The UMD-MSH2 mutations database
Record ID: 2098

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS12-6T>C (c.2006-6T>C)

wt codonwt aamutant codonmutant aamutational eventmutation type
GGCGlyspl-6Spl.T>C

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 _
tttgttctgtagGC
86.7 _
0.8 %

Patient and sample data


Sample IDPatient status
7_5393 (05K274)4965E06010Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data