The UMD-APC mutations database
Record ID: 4215

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.1824insAp.Val609CysfsX25

wt codonwt aamutant codonmutant aamutational eventmutation type
GCTAlains1cFs.Stop at 633

StructureKey Residue (HCD)Pyrimidin doubletCpG
ASEF binding domain ARM4 

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_-1792G00427G00427Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data