Nucleotide substitution: C?T.
Base change GCC->GTC.
Fmr1A158V.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: A158V.
C10105677T
C?T
A158V | Fmr1-PA; A158V | Fmr1-PB; A158V | Fmr1-PC; A158V | Fmr1-PD; A120V | Fmr1-PE; A120V | Fmr1-PF; A206V | Fmr1-PG; A206V | Fmr1-PH; A120V | Fmr1-PI; A158V | Fmr1-PJ; A158V | Fmr1-PK
A158V
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.