CYP4A11 allele nomenclature

*Allele*	*Protein*	Nucleotide changes, Gene	*Effect*	*Enzyme_activity*		*References*
*Allele*	*Protein*	Nucleotide changes, Gene	*Effect*	*In_vivo*	*In vitro*	*References*
CYP4A111*	CYP4A11.1	None	None
Additional SNPs, where the haplotype has not yet been determined
		4126T>C	W126R			NCBI dbSNP
		4648G>A	G130S			NCBI dbSNP
		4714T>A	Y152N			NCBI dbSNP
		5829G>T	V185F			NCBI dbSNP
		6911A>C	K276T			NCBI dbSNP
		7227A>G	S353G			Cho et al., 2005
		8447C>T	P428L			NCBI dbSNP
		8610T>C	F434S	Incr. risk for hypertension	Decr.	Gainer et al., 2005 Mayer et al., 2005
		11284C>T	L509F			NCBI dbSNP

Changes made since the last update (27-Mar-2007) are marked in red.

Links to the NCBI dbSNP homepage are available for functional SNPs when present in NCBI's database.

Nucleotide variations in bold are the major SNPs/alterations responsible for the phenotype of the corresponding allele.