The UMD-APC mutations database
Record ID: 3128

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.2385_2386delCTp.Tyr796TrpfsX2

wt codonwt aamutant codonmutant aamutational eventmutation type
CTCLeudel2cFs.Stop at 797Fr.

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
33_PSL2995---10-236Relative

Clinical data


Symptom

Reference


Reference IDReference
33Unpublished data