The UMD-APC mutations database
Record ID: 2218

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.3901_3905delACCCTp.Thr1301AlafsX12

wt codonwt aamutant codonmutant aamutational eventmutation type
ACCThrdel5aFs.Stop at 1312Fr.

StructureKey Residue (HCD)Pyrimidin doubletCpG
 

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_32697---32697Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data