The UMD-MSH2 mutations database
Record ID: 3172

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.571_573delCTCp.Leu191del

wt codonwt aamutant codonmutant aamutational eventmutation type
CTCLeudel3aInFIn frame delInF

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
17_130837917314001---Relative

Clinical data


Symptom

Reference


Reference IDReference
17Unpublished data