The UMD-MSH2 mutations database
Record ID: 454

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.508C>Tp.Gln170X

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
8_34479_4051966_08-922280Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data