The UMD-MSH2 mutations database
Record ID: 849

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.646_792delp.Ile216_Gln264del

wt codonwt aamutant codonmutant aamutational eventmutation type
ATAIledel147aInFIn frame delInF

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
19_6509_6509-002_6509-002Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data