The UMD-MSH2 mutations database
Record ID: 776

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2292G>Ap.Trp764X

wt codonwt aamutant codonmutant aamutational eventmutation type
TGGTrpTGAStopG->ATs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 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
19_14997_14997-003_14997-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data