The UMD-APC mutations database
Record ID: 2159

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.4666delAp.Thr1556LeufsX9

wt codonwt aamutant codonmutant aamutational eventmutation type
ACTThrdel1aFs.Stop at 1564Fr.

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_30381---30381Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data