Amino acid replacement: V775D.
T8068632A
V775D | mys-PA; V775D | mys-PB; V775D | mys-PC; V775D | mys-PD
V775D
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.