The UMD-APC mutations database
Record ID: 5092

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2275delGp.Ala759ProfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
GCCAladel1aFs.Stop at 760Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ASEF binding domain ARM7 

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_-732G05336G05336Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data