The UMD-MSH2 mutations database
Record ID: 910

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2009C>Tp.Pro670Leu

wt codonwt aamutant codonmutant aamutational eventmutation type
CCCProCTCLeuC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 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)
0.990.00 (pathogenous)71 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
20_20-2819_2819-02_12049Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data