Amino acid replacement: L188F.
Missense mutation in the helicase domain.
C17580245T
L188F | Dcr-2-PA; L188F | Dcr-2-PB
L188F
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Dcr-2L188F is a suppressor of abnormal eye color phenotype of wRNAi.GMR
wIR.GMR eyes that are also homozygous for Dcr-2L188F show stronger eye pigmentation compared to wIR.GMR eyes.