The UMD-MSH2 mutations database
Record ID: 3151

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.IVS15-106T>A (c.2635-106T>A)

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnspl-106Spl.T>A

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 (%)

Patient and sample data


Sample IDPatient status
31_H1814H1814-1H1814-1ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data