The UMD-MSH2 mutations database
Record ID: 277

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1661G>Cp.Ser554Thr

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerACCThrG->CTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 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)
10.21 (non pathogenous)88 (Pathogenous)

Patient and sample data


Sample IDPatient status
5_1995020_20082736_AAC588Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data