Polytene chromosomes normal.
Amino acid replacement: L223F.
Nucleotide substitution: A669T.
The nucleotide substitution A669T results in the L223F amino acid replacement. The mutant allele also contains the nucleotide polymorphism C2102A, which results in a P701H protein polymorphism (coordinates of the lesions are the position in the 2-μ-4a spliced form of pb).
Amino acid replacement: P701H.
Nucleotide substitution: C2102A.
A6711847T
A669T
L223F | pb-PA; L218F | pb-PB; L218F | pb-PC; L213F | pb-PD
L223F
A polymorphism (P701H) is also seen in this strain. Reported coordinates are with respect to pb-RA and pb-PA.
Cain.