Amino acid replacement: C701Y.
G8068410A
C701Y | mys-PA; C701Y | mys-PB; C701Y | mys-PC; C701Y | mys-PD
C701Y
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Weak allele.
Selected as: a mutation that permits the survival of an F1 male.