Nucleotide substitution: T275A. Nucleotide substitution: C338A. Nucleotide substitution: G368A. Nucleotide substitution: C382G. Nucleotide substitution: T433C. Nucleotide substitution: T494C. Nucleotide substitution: C518T. Nucleotide substitution: A544G. Nucleotide substitution: C570T. Nucleotide substitution: T589G. Nucleotide substitution: G643T. Nucleotide substitution: G653T. Nucleotide substitution: A662G. Nucleotide substitution: A690C. Nucleotide substitution: C1254T. Nucleotide substitution: G1387T. Nucleotide substitution: A1570T. Nucleotide substitution: A1955G. Nucleotide substitution: A1985G. Nucleotide substitution: T2089C. Nucleotide substitution: A2092G. Nucleotide substitution: T2093C. Nucleotide substitution: T2173C. Nucleotide substitution: T2250C. Nucleotide substitution: G2272T. Nucleotide substitution: T2294C. Nucleotide substitution: C2305T. Nucleotide substitution: C2417T. Nucleotide substitution: G2803A. Nucleotide substitution: C2874A. Nucleotide substitution: A2889C. Nucleotide substitution: A2922G. Nucleotide substitution: A2923C. Nucleotide substitution: T2941G. Nucleotide substitution: T2996A. Nucleotide substitution: T3022C. 5bp deletion of CTTTT starting at nucleotide position 325. Also lacks the 35bp insertion starting at nucleotide position 392 which is present in the "S26-F" strain. (Substitutions are relative to the "S26-F" strain. Transcription start site corresponds to nucleotide position 1184).