The UMD-MSH2 mutations database
Record ID: 200

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2111T>Cp.Ile704Thr

wt codonwt aamutant codonmutant aamutational eventmutation type
ATTIleACTThrT->CTs

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)
10.00 (pathogenous)88 (Pathogenous)

Patient and sample data


Sample IDPatient status
4_BCR0910_23796_2890Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data