Nucleotide substitution: G?A. Mutation in a splice acceptor site, which is predicted to disrupt the joining of exon 11 to exon 12.
G26699449A
G?A
Splice acceptor site mutation.
lethal | embryonic stage (with Df(3R)Tl-X)
lethal | larval stage (with Df(3R)Tl-X)
lethal | recessive