The UMD-APC mutations database
Record ID: 2788

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.5514delTp.Phe1838LeufsX25

wt codonwt aamutant codonmutant aamutational eventmutation type
TTTPhedel1cFs.Stop at 1862Fr.

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
19_6062---6062.003Relative

Clinical data


Symptom

Reference


Reference IDReference
19Unpublished data