The UMD-MSH2 mutations database
Record ID: 2951

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2038C>Ap.Arg680Arg

wt codonwt aamutant codonmutant aamutational eventmutation type
CGAArgAGAArgC->ATv

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 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)
0.991.00 (non pathogenous)18 (Polymorphism)

Patient and sample data


Sample IDPatient status
4_11165266403652Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data