Amino acid replacement: W3406term.
G5920891A
W3406term | bchs-PA
W3406term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
bchs10 mutants show no defects in the larval visual system or embryonic central nervous system.