The UMD-MSH2 mutations database
Record ID: 138

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1_1276delp.Met1?

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel1276aFs.Stop at 12Fr.

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
4_H-H05043_19298_1462Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data