The UMD-MSH2 mutations database
Record ID: 186

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1881A>Cp.Lys627Asn

wt codonwt aamutant codonmutant aamutational eventmutation type
AAALysAACAsnA->CTv

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)
10.05 (pathogenous)68 (Probably pathogenous)

Patient and sample data


Sample IDPatient status
4_B9707_---_---Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data