Nucleotide substitution: C?T.
Amino acid replacement: Q196term.
Fmr1Q196Stop.EP3517 carries both the P{EP} insertion present in the progenitor allele and the nonsense mutation in the Fmr1 coding region.
C10105564T
C?T
Q196term | Fmr1-PA; Q196term | Fmr1-PB; Q196term | Fmr1-PC; Q196term | Fmr1-PD; Q158term | Fmr1-PE; Q158term | Fmr1-PF; Q244term | Fmr1-PG; Q244term | Fmr1-PH; Q158term | Fmr1-PI; Q196term | Fmr1-PJ; Q196term | Fmr1-PK
Q196term
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.