The UMD-APC mutations database
Record ID: 5558

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.3579_3582delGTCAp.Gln1193HisfsX71

wt codonwt aamutant codonmutant aamutational eventmutation type
CAGGlndel4cFs.Stop at 1263Fr.

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_-6086ILP0512141E051246Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data