One PubMed reference (PMID: 21806386) indicates that corresponds with CYP3A5*6. However, this seems doubtful. CYP3A5 allele nomenclature found at http://www.cypalleles.ki.se/cyp3a5.htm indicates that CYP3A5*6 (also known as 14690G>A) is a splicing defect resulting in essentially no activity in the gene. This does not correspond with dbSNP, which indicates that is a nucleotide substition (624G-A) which only results in a "silent" substitution of AAG (Lysine) to AAA (Lysine).
- Agreed. Adjusted. Appreciated. --- cariaso 12:31, 20 March 2013 (UTC)