The UMD-MSH2 mutations database
Record ID: 697

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1528C>Tp.Gln510X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlnTAGStopC->TTs

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 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
19_7803_7803-002_7803-002Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data