The UMD-APC mutations database
Record ID: 3676

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2490_2491delGTp.Leu831ThrfsX12

wt codonwt aamutant codonmutant aamutational eventmutation type
GTGValdel2cFs.Stop at 842Fr.

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_-395955955Relative

Clinical data


Symptom

Reference


Reference IDReference
71Unpublished data