The UMD-MSH2 mutations database
Record ID: 3098

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1662_2458delp.Ser554ArgfsX4

wt codonwt aamutant codonmutant aamutational eventmutation type
AGCSerdel797cFs.Stop at 557Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Lever 

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
17_141124718726001---Relative

Clinical data


Symptom

Reference


Reference IDReference
17Unpublished data