Nucleotide substitution: G?A.
Base change GGC->GAC.
Fmr1G80D.EP3517 carries both the P{EP} insertion present in the progenitor allele and the amino acid replacement in the Fmr1 coding region.
Amino acid replacement: G80D.
G10105976A
G?A
G80D | Fmr1-PA; G80D | Fmr1-PB; G80D | Fmr1-PC; G80D | Fmr1-PD; G42D | Fmr1-PE; G42D | Fmr1-PF; G128D | Fmr1-PG; G128D | Fmr1-PH; G42D | Fmr1-PI; G80D | Fmr1-PJ; G80D | Fmr1-PK
G80D
Selected as: A mutation that suppresses the lethality caused when a Scer\GAL4 driver is used to overexpress Fmr1 from the P{EP}Fmr1EP3517 insertion.