The UMD-APC mutations database
Record ID: 5696

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.4881delAp.Lys1628SerfsX22

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlndel1cFs.Stop at 1649Fr.

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_-5726ILP0711254E071527Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data