The UMD-MSH2 mutations database
Record ID: 751

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.198C>Gp.Tyr66X

wt codonwt aamutant codonmutant aamutational eventmutation type
TACTyrTAGStopC->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 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
19_2543_2543-006_2543-006Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data