The UMD-APC mutations database
Record ID: 4418

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2614_2636delp.Thr872AspfsX32

wt codonwt aamutant codonmutant aamutational eventmutation type
ACTThrdel23aFs.Stop at 903Fr.

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
SO_-259G01388G01388Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data