The UMD-MSH2 mutations database
Record ID: 995

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1874delTp.Leu625TrpfsX10

wt codonwt aamutant codonmutant aamutational eventmutation type
TTGLeudel1bFs.Stop at 634Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ATPase 

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
31_H436_H436-2_H436-2ARelative

Clinical data


Symptom

Reference


Reference IDReference
31Unpublished data