The UMD-MSH2 mutations database
Record ID: 1090

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1delAp.Met1?

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel1aFs.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
37_L11.022_19412_128246Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data