Nucleotide substitution: C338A. Nucleotide substitution: G368A. Nucleotide substitution: T494C. Nucleotide substitution: C518T. Nucleotide substitution: C532G. Nucleotide substitution: A544G. Nucleotide substitution: C570T. Nucleotide substitution: T589G. Nucleotide substitution: G643T. Nucleotide substitution: G653T. Nucleotide substitution: A662G. Nucleotide substitution: A690C. Nucleotide substitution: A1501G. Nucleotide substitution: C1561T. Nucleotide substitution: T1774C. Nucleotide substitution: T1888C. Nucleotide substitution: A1955G. Nucleotide substitution: A1985G. Nucleotide substitution: C2032T. Nucleotide substitution: T2089C. Nucleotide substitution: A2092G. Nucleotide substitution: T2093C. Nucleotide substitution: T2408G. Nucleotide substitution: T2551C. Nucleotide substitution: T2588A. Nucleotide substitution: A2629G. Nucleotide substitution: T2756G. Nucleotide substitution: G2936T. Nucleotide substitution: G2953A. 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).