The UMD-MSH2 mutations database
Record ID: 1206

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.126delCp.Tyr43IlefsX21

wt codonwt aamutant codonmutant aamutational eventmutation type
TTCPhedel1cFs.Stop at 63Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Mismatch binding 

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_L10.075_19883_130655Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data