Acceptor site of intron 3 change AG->TG, resulting in frameshift from V35.
Fmr1X22.EP3517 carries both the P{EP} insertion present in the progenitor allele and the rearrangement involving Fmr1.
A10107481T
AG to TG change in splice acceptor site leads to a frameshift from G18.
A mutation that suppresses the lethality caused when a Scer\GAL4 driver is used to overexpress Fmr1 from the P{EP}Fmr1EP3517 insertion.
Separable from: P{EP}Fmr1EP3517.