The UMD-MSH2 mutations database
Record ID: 3256

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS13-14A>C (c.2211-14A>C)

wt codonwt aamutant codonmutant aamutational eventmutation type
AGGArgspl-14Spl.A>C

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

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
tatgtgcttcagGT
89.1 _
ctatgtgcttcagGT
21.4 _ *
-76 %

Patient and sample data


Sample IDPatient status
8_466718967908-367141Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data