Amino acid replacement: L224F.
C8064700T
L224F | mys-PA; L224F | mys-PB; L224F | mys-PC; L224F | mys-PD
L224F
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. Same mutation as mysb61.
Weak allele.
Selected as: a mutation that permits the survival of an F1 male.