The UMD-APC mutations database
Record ID: 2193

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.3186_3187delAAp.Ser1063X

wt codonwt aamutant codonmutant aamutational eventmutation type
CAAGlndel2cFs.Stop at 1063Fr.

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
4_19451---19451Relative

Clinical data


Symptom

Reference


Reference IDReference
4Unpublished data