The UMD-MSH2 mutations database
Record ID: 779

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2336delTp.Met779SerfsX33

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel1bFs.Stop at 811Fr.

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
19_11997_11997-001_11997-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data