The UMD-MSH2 mutations database
Record ID: 3139

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2430C>Gp.Thr810Thr

wt codonwt aamutant codonmutant aamutational eventmutation type
ACCThrACGThrC->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase Yes, 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)
0.980.67 (non pathogenous)18 (Polymorphism)

Patient and sample data


Sample IDPatient status
37_L13.13816818147896Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data