The UMD-MSH2 mutations database
Record ID: 2357

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.749delGp.Gly250GlufsX4

wt codonwt aamutant codonmutant aamutational eventmutation type
GGAGlydel1bFs.Stop at 253Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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
SO_-2088---G00872Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data