Nucleotide substitution: A352G. Nucleotide substitution: A362T. Nucleotide substitution: C478T. Nucleotide substitution: T534A. Nucleotide substitution: T539G. Nucleotide substitution: A626G. Nucleotide substitution: C635A. Nucleotide substitution: C731T. Nucleotide substitution: G759A. Nucleotide substitution: C818T. Nucleotide substitution: G820A. Nucleotide substitution: G907A. Nucleotide substitution: T921A. Nucleotide substitution: T931C. Nucleotide substitution: C1114T. Nucleotide substitution: T1162C. Nucleotide substitution: T1248C. Nucleotide substitution: C1299T. Nucleotide substitution: T1380C. Nucleotide substitution: T1645A. Nucleotide substitution: C1648T. Nucleotide substitution: C1658A. Nucleotide substitution: C1673A. Nucleotide substitution: A1781G. Nucleotide substitution: C1784T. Nucleotides 537 and 834 are absent (relative to the consensus haplotype). Nucleotide 1646 (which is absent in the consensus haplotype) is: A. Nucleotides are numbered relative to the first position of the start codon, which is numbered as +80.
Isolated from: Kyoto, Japan population (July 2002).