The UMD-APC mutations database
Record ID: 5043

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1847delTp.Leu616TrpfsX14

wt codonwt aamutant codonmutant aamutational eventmutation type
TTGLeudel1bFs.Stop at 629Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ASEF binding domain ARM4 

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_-3670G05077G05077Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data