The UMD-MSH2 mutations database
Record ID: 1075

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.20delAp.Glu7GlyfsX57

wt codonwt aamutant codonmutant aamutational eventmutation type
GAGGludel1bFs.Stop at 63Fr.

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
33_TNN193__03-099Relative

Clinical data


Symptom

Reference


Reference IDReference
33Unpublished data