Nucleotide substitution: T?C. Amino acid replacement: I11T. Nucleotide substitution: C?G and G?A. Amino acid replacement: Q19E.
T14972770C
T?C
I11T | Brd-PA
I11T
Mutation induced on Brd1 chromosome; one of three base pair changes in mutan, two of which occur in the same codon.
C14972793G
C?G
Q19E | Brd-PA
Q19E
Mutation induced on Brd1 chromosome; one of three base pair changes in mutant, two of which occur in codon Q19 (CAG to GAA).
Viable when heterozygous with Df(3L)Brd12, adults exhibit no external mutant phenotype.
Leviten.
Revertant.
Brd bristle multiplication phenotype is reverted.