The UMD-MSH2 mutations database
Record ID: 1318

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.454delAp.Met152CysfsX22

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel1aFs.Stop at 173Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
Connector 

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_L08.049_9112_79514Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data