The UMD-APC mutations database
Record ID: 3637

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2033delGp.Ser678IlefsX40

wt codonwt aamutant codonmutant aamutational eventmutation type
AGTSerdel1bFs.Stop at 717Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ASEF binding domain ARM5 

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
SO_-332792792Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data