The UMD-APC mutations database
Record ID: 5702

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1313_1408delp.Met438_Gly470delinsArg

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel96bInFIn frame delInF

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
7_-3173ILP0711663E072047Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data