The UMD-APC mutations database
Record ID: 5646

Mutation description


Variation name (cDNA level)Variation name (protein level)Variation status
c.3736delGp.Ala1246LeufsX19

wt codonwt aamutant codonmutant aamutational eventmutation type
GCTAladel1aFs.Stop at 1264Fr.

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_-1155ILP0612098E061737-Relative

Clinical data


Symptom

Reference


Reference IDReference
7Unpublished data