Amino acid replacement: R269W.
Missense mutation in the helicase domain.
C17579946T
R269W | Dcr-2-PA; R269W | Dcr-2-PB
R269W
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Dcr-2R269W is a suppressor of abnormal eye color phenotype of wRNAi.GMR
wIR.GMR eyes that are also homozygous for Dcr-2R269W show stronger eye pigmentation compared to wIR.GMR eyes.