The UMD-APC mutations database
Record ID: 2202

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1861_1864delACTTp.Tyr622GlyfsX7

wt codonwt aamutant codonmutant aamutational eventmutation type
ACTThrdel4aFs.Stop at 628Fr.

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
4_28210---28210Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data