The UMD-MSH2 mutations database
Record ID: 422

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1627delGp.Asp543IlefsX14

wt codonwt aamutant codonmutant aamutational eventmutation type
GATAspdel1aFs.Stop at 556Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
EXO1 stabilization 

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_43171_9031973_08-202201Relative

Clinical data


Symptom

Reference


Reference IDReference
8Unpublished data