Amino acid replacement: T559K.
Amino acid replacement: L561R.
T7221206G
L561R | mEFG1-PA
L561R
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
C7221212A
T559N | mEFG1-PA
T559K
The mutation is reported as T559K but a single missense mutation in the codon leads to T559N. It may be a strain difference or a mutation of two adjacent nucleotides.
Fewer than expected homozygous icoGA1 clones survive to adulthood in the eye.