The UMD-MSH2 mutations database
Record ID: 315

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2152C>Tp.Gln718X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlnTAAStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase Yes, 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
5_2002201_20024934_---Relative

Clinical data


Symptom

Reference


Reference IDReference
5Unpublished data