The UMD-MSH2 mutations database
Record ID: 444

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.264delTp.Phe88LeufsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
TTTPhedel1cFs.Stop at 89Fr.

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
8_42232_15041971_08-32700Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data