The UMD-MSH2 mutations database
Record ID: 1244

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2017G>Tp.Gly673X

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlyTGAStopG->TTv

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATP binding 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
37_L03.19_1693_15109Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data