Nucleotide substitution: T11G. Nucleotide substitution: G24C. Nucleotide substitution: A67G. Nucleotide substitution: G549C. Nucleotide substitution: A696G. Nucleotide substitution: T713G. Nucleotide substitution: G820T. Nucleotide substitution: A926G. Nucleotide substitution: C1018T. Nucleotide substitution: C1114T. Nucleotide substitution: T1162C. Nucleotide substitution: G1224A. Nucleotide substitution: T1248C. Nucleotide substitution: A1272C. Nucleotide substitution: T1645A. Nucleotide substitution: A1650T. Nucleotide substitution: A1656T. Nucleotide substitution: C1659T. Nucleotide substitution: T1662A. Nucleotide substitution: C1691T. Nucleotide substitution: A1692G. Nucleotide substitution: A1693T. Nucleotides 46-51 (which are absent in the consensus haplotype) are: TTAGTC. Nucleotides are numbered relative to the first position of the start codon, which is numbered as +80.
Isolated from: Kyoto, Japan population (July 2002).