The UMD-MSH2 mutations database
Record ID: 2257

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.350G>Ap.Trp117X

wt codonwt aamutant codonmutant aamutational eventmutation type
TGGTrpTAGStopG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding Yes, non coding strandNo

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
7_1215715203E120033Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data