The UMD-MSH2 mutations database
Record ID: 785

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2499delTp.Ala834LeufsX7

wt codonwt aamutant codonmutant aamutational eventmutation type
CTTLeudel1cFs.Stop at 840Fr.

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_14321_14321-001_14321-Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data