Amino acid replacement: P1496L.
Missense mutation in the RNase IIIb domain.
C17576077T
P1496L | Dcr-2-PA; P1495L | Dcr-2-PB
P1496L
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Dcr-2P1496L is a suppressor of abnormal eye color phenotype of wRNAi.GMR
wIR.GMR eyes that are also homozygous for Dcr-2P1496L show stronger eye pigmentation compared to wIR.GMR eyes.