Nucleotide substitution: A?T.
Amino acid replacement: K215term.
Fmr1K215Stop.EP3517 carries both the P{EP} insertion present in the progenitor allele and the nonsense mutation in the Fmr1 coding region.
A10105450T
A?T
K215term | Fmr1-PA; K215term | Fmr1-PB; K215term | Fmr1-PC; K215term | Fmr1-PD; K177term | Fmr1-PE; K177term | Fmr1-PF; K263term | Fmr1-PG; K263term | Fmr1-PH; K177term | Fmr1-PI; K215term | Fmr1-PJ; K215term | Fmr1-PK
K215term
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.