The UMD-MSH6 mutations database
Record ID: 2114

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1641A>Cp.Glu547Asp

wt codonwt aamutant codonmutant aamutational eventmutation type
GAAGluGACAspA->CTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector Yes, non coding strandNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Conservation (0-1)SIFT (0-1)UMD-predictor (0-100)
0.860.51 (non pathogenous)23 (Polymorphism)

Patient and sample data


Sample IDPatient status
4_Gr2012-7035677---Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data