Variants | cDNA Change | Location | Amino Acid Change | Allele No. or dbSNP Identification No. | Allele Frequencya | ||
---|---|---|---|---|---|---|---|
Whites | Blacks | Asians | |||||
CYP2C19.1A | None | None | CYP2C19*1A | ||||
CYP2C19.1B | 99C>T, 991A>G | Exon7 | I331V | CYP2C19*1B | N.R. | N.R. | 0.6–0.955 (1,2) |
CYP2C19.5B | 99C>T, 991A>G, 1297C>T | Exon9 | I331V, R433W | CYP2C19*5B | 0 (3) | N.R. | 0–0.001 (3) |
CYP2C19.6 | 99C>T, 395G>A, 991A>G | Exon3 | R132Q, I331V | CYP2C19*6 | 0–0.003 (4) | N.R. | N.R. |
CYP2C19.8 | 99C>T, 358T>C | Exon3 | W120R | CYP2C19*8 | 0–0.007 (5) | N.R. | N.R. |
CYP2C19.9 | 991A>G | Exon3 | R144H, I331V | CYP2C19*9 | 0–0.0029 (6–8) | 0.04–0.06 (6,7) | 0 (6,7) |
CYP2C19.10 | 99C>T, 680C>T, 991A>G | Exon5 | P227L, I331V | CYP2C19*10 | 0 (6,8) | 0.02 (6) | 0 (6) |
CYP2C19.11 | 99C>T, 449G>A, 991A>G | Exon3 | R150H, I331V | CYP2C19*11 | 0–0.03 (6,8) | 0 (6) | 0 (6) |
CYP2C19.13 | 99C>T, 991A>G, 1228C>T | Exon8 | I331V, R410C | CYP2C19*13 | 0 (6,8) | 0.02 (6) | 0 (6) |
CYP2C19.14 | 96C>T, 99C>T, 991A>G | Exon1 | L17P, I331V | CYP2C19*14 | 0 (6) | 0.02 (6) | 0 (6) |
CYP2C19.15 | 55A>C, 99C>T | Exon1 | I19L | CYP2C19*15 | 0 (6) | 0.02 (6) | 0 (6) |
CYP2C19.16 | 99C>T, 1324C>T | Exon9 | R442C | CYP2C19*16 | N.R. | N.R. | 0–0.017 (9) |
CYP2C19.18 | 99C>T, 986G>A; | Exon7 | R329H | CYP2C19*18 | N.R. | N.R. | 0.002 (1) |
CYP2C19.19 | 99C>T, 151A>G; | Exon1 | S51G | CYP2C19*19 | N.R. | N.R. | 0.002 (1) |
E92D | 99C>T, 276G>C, 991A>G | Exon2 | E92D, I331V | CYP2C19*2B | 0.02–0.0047 (6,8) | 0 (6) | 0 (6) |
A161P | 99C>T, 481G>C, 991A>G, | Exon3 | A161P, I331V | CYP2C19*2C | N.R. | N.R. | 0.006 (1) |
D360N | 99C>T, 991A>G, 1078G>A | Exon7 | D360N, I331V | CYP2C19*3B | N.R. | N.R. | 0.002–0.02 (1,2) |
M74T | 221T>C | Exon2 | M74T | rs28399505 | 0 (7) | 0 (7) | 0.05 (7) |
F168L | 502T>C | Exon4 | F168L | rs28399510 | 0.02 (7) | 0 (7) | 0 (7) |
E122A | 356A>C | Exon3 | E122A | rs17885179 | 0.006 (mixed population in North America) (10) | ||
W212C | 636G>T | Exon4 | W212C | rs4986893 |
N.R., not reported.
↵a The allele frequencies are from the following references: 1, Fukushima-Uesaka et al. (2005); 2, Zhou et al. (2009); 3, Ibeanu et al. (1998a); 4, Ibeanu et al. (1998b); 5, Ibeanu et al. (1999); 6, Blaisdell et al. (2002); 7, Solus et al. (2004); 8, Nakamoto et al. (2007); 9, Morita et al. (2004); and 10, http://www.ncbi.nlm.nih.gov/snp/.