The UMD-APC mutations database
Record ID: 4767

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2756delGp.Arg919LysfsX36

wt codonwt aamutant codonmutant aamutational eventmutation type
AGAArgdel1bFs.Stop at 954Fr.

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
SO_-3363G03667G03667Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data