The UMD-MSH2 mutations database
Record ID: 1222

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1835C>Gp.Ser612X

wt codonwt aamutant codonmutant aamutational eventmutation type
TCASerTGAStopC->GTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
Lever 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
37_L10.067_11968_101745Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data