The UMD-MSH2 mutations database
Record ID: 2302

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1967A>Gp.Tyr656Cys

wt codonwt aamutant codonmutant aamutational eventmutation type
TACTyrTGCCysA->GTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase NoNo

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)
10.03 (pathogenous)86 (Pathogenous)

Patient and sample data


Sample IDPatient status
7_1255285E2K268Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data