Amino acid replacement: V409D.
Amino acid replacement: V409D. Nucleotide substitution: T1226A.
T8067471A
V409D | mys-PA; V409D | mys-PB; V409D | mys-PC; V409D | mys-PD
V409D
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.