Contains an insertion of an extra base C at nt 2457, an extra base C at nt 1234, a 14bp insertion of ATAGAGAAATTATC at nt 2622, a 6bp insertion of TTTTTC at nt 2650 and a 4bp insertion of AGTA at nt 2663. Contains a deletion of the sequence ATTGT at nucleotide 2151 onwards and a deletion of the base A at 526. Nucleotide positions correspond to GenBank accession X04426. Substitutions are relative to DdcR6, GenBank accession AY197756.
Nucleotide substitution: C420T.
Nucleotide substitution: T440G.
Nucleotide substitution: T507A.
Nucleotide substitution: A517T.
Nucleotide substitution: T644G.
Nucleotide substitution: C758T.
Nucleotide substitution: G916A.
Nucleotide substitution: T928C.
Nucleotide substitution: G1690A.
Nucleotide substitution: C1790T.
Nucleotide substitution: C1803T.
Nucleotide substitution: C1923G.
Nucleotide substitution: A1926T.
Nucleotide substitution: T1932C.
Nucleotide substitution: T1957C.
Nucleotide substitution: G1972A.
Nucleotide substitution: C1981T.
Nucleotide substitution: A2014G.
Nucleotide substitution: A2116G.
Nucleotide substitution: C2155A.
Nucleotide substitution: A2173G.
Nucleotide substitution: C2365T.
Nucleotide substitution: A2413T.
Nucleotide substitution: A2452C.
Nucleotide substitution: G2453C.
Nucleotide substitution: T2454C.
Nucleotide substitution: T2455A.
Nucleotide substitution: A2594G.
Nucleotide substitution: T2598C.
Nucleotide substitution: G2610A.
Nucleotide substitution: A2614T.
Nucleotide substitution: C2640T.
Nucleotide substitution: T2642A.
Nucleotide substitution: A2648T.
Nucleotide substitution: C2665T.
Nucleotide substitution: T2738G.
Nucleotide substitution: A2860T.
Nucleotide substitution: T3068A.
Nucleotide substitution: A3554G.
Nucleotide substitution: T4214C.
Nucleotide substitution: C4497A.
Nucleotide substitution: A4498T.
Nucleotide substitution: T4654G.
Nucleotide substitution: G4694A.
Nucleotide substitution: A4939C.
Isolated from: Raleigh, North Carolina, USA, 1999