The UMD-MSH2 mutations database
Record ID: 3218

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.643C>Tp.Gln215X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlnTAGStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector NoNo

Mutation impact


At the mRNA levelOn restriction map
New restriction site(s): none
Lost restriction site(s): none

Patient and sample data


Sample IDPatient status
20_20-43654365-01---Relative

Clinical data


Symptom

Reference


Reference IDReference
20Unpublished data