The UMD-APC mutations database
Record ID: 3117

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.598delAp.Met200TrpfsX5

wt codonwt aamutant codonmutant aamutational eventmutation type
ATGMetdel1aFs.Stop at 204Fr.

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
33_PSL3315---10-1262Relative

Clinical data


Symptom

Reference


Reference IDReference
33Unpublished data