The UMD-APC mutations database
Record ID: 4395

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2204delCp.Ala735GlyfsX26

wt codonwt aamutant codonmutant aamutational eventmutation type
GCGAladel1bFs.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_-1865G01305G01305Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data