The UMD-MSH2 mutations database
Record ID: 119

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.638_639delTGp.Leu213GlnfsX18

wt codonwt aamutant codonmutant aamutational eventmutation type
CTGLeudel2bFs.Stop at 230Fr.

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
2_02-DDM6018_24616_24616Relative

Clinical data


Symptom

Reference


Reference IDReference
2Unpublished data