Amino acid replacement: V763M.
G8068595A
V763M | mys-PA; V763M | mys-PB; V763M | mys-PC; V763M | mys-PD
V763M
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.