The UMD-MSH2 mutations database
Record ID: 373

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.226C>Tp.Gln76X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlnTAGStopC->TTs

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
6_603018_200500499_S3554Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data