The UMD-MSH2 mutations database
Record ID: 901

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS7-2A>C (c.1277-2A>C)

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlyspl-2Spl.A>C

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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
actttcttttagGA
84.4 _
actttcttttcgGA
55.5 _ *
-34.3 %

Patient and sample data


Sample IDPatient status
20_20-1503_1503-14_5054Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data