Deletion of bases 6582-6590 replaced by a T insertion in intron 5, resulting in no amino acid change.
Fmr1X1.EP3517 carries both the P{EP} insertion present in the progenitor allele and the rearrangement involving Fmr1.
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.