The UMD-MSH2 mutations database
Record ID: 811

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.425C>Ap.Ser142X

wt codonwt aamutant codonmutant aamutational eventmutation type
TCASerTAAStopC->ATv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 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
19_4768_4768-003_4768-003Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data