Amino acid replacement: L695F.
Amino acid alteration. In addition, the P{GSV6}Nedd4GS13178 insertion is still present on the chromosome.
C17544472T
L481F | Nedd4-PE; L644F | Nedd4-PF; L619F | Nedd4-PG; L682F | Nedd4-PH; L671F | Nedd4-PI; L695F | Nedd4-PJ; L522F | Nedd4-PK; L693F | Nedd4-PL; L687F | Nedd4-PM
L695F
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The P{GSV6}Nedd4GS13178 insertion is still present on the chromosome.
viable, with Scer\GAL4da.G32
Selected as: a revertant of the larval lethality caused by expression of Nedd4GS13178 under the control of Scer\GAL4da.G32.