The UMD-MSH2 mutations database
Record ID: 457

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.518T>Cp.Leu173Pro

wt codonwt aamutant codonmutant aamutational eventmutation type
CTALeuCCAProT->CTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 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)
0.980.00 (pathogenous)71 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
8_34876_11081924_B051630Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data