The UMD-APC mutations database
Record ID: 3283

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1726delGp.Ala576LeufsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
GCTAladel1aFs.Stop at 577Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
ASEF binding domain ARM3 

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
37_P99.05241---Relative

Clinical data


Symptom

Reference


Reference IDReference
37Unpublished data