The UMD-MSH6 mutations database
Record ID: 2030

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.3724_3726delCGTp.Arg1242del

wt codonwt aamutant codonmutant aamutational eventmutation type
CGTArgdel3aInFIn frame delInF

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
37_L14.12626170160524Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data