The UMD-MSH2 mutations database
Record ID: 912

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2154A>Gp.Gln718Gln

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnCAGGlnA->GTs

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

Patient and sample data


Sample IDPatient status
20_20-1195_1195-05_---Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data