The UMD-APC mutations database
Record ID: 2152

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1201delAp.Arg401GlyfsX53

wt codonwt aamutant codonmutant aamutational eventmutation type
AGGArgdel1aFs.Stop at 453Fr.

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_20876---20876Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data