The UMD-MSH2 mutations database
Record ID: 701

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1660A>Tp.Ser554Cys

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerTGCCysA->TTv

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)
10.01 (pathogenous)70 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
19_11296_11296-003_11296-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data