TABLE 3

Human GSTO1 haplotypes with frequencies ≥1%

If a haplotype included a variant amino acid sequence, it was included in the table even if its frequency fell below the 1% cutoff. Nucleotide positions are numbered as described in the legend for Table 1. Variant nucleotides compared with the ′reference sequence′, i.e., the most common sequence in AA subject, are highlighted as white type against a black background. The initial column lists ′observed′ (o) and inferred (i) haplotypes. ′D′ indicates a 3-bp deletion. Dashes represent lack of that haplotype in the population indicated.