Amino acid replacement: R676C.
C8068334T
R676C | mys-PA; R676C | mys-PB; R676C | mys-PC; R676C | mys-PD
R676C
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.