The UMD-MSH2 mutations database
Record ID: 379

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.279_281delTCTp.Leu94del

wt codonwt aamutant codonmutant aamutational eventmutation type
CTTLeudel3cInFIn frame delInF

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
6_609051_B67182_S6550Relative

Clinical data


Symptom

Reference


Reference IDReference
6Unpublished data