C166term | CG17683-PA; C162term | CG17683-PC; C119term | CG17683-PD
Location of the mutation written as the number of nucleotides downstream of the predicted translation start site.
Nucleotide substitution: T602A.
Amino acid replacement: C?term.
lethal (with CG1768334-13)
lethal (with CG17683NC37)
lethal (with CG17683NC70)
lethal (with CG17683NC109)
lethal (with Df(2R)34-2)
lethal (with Df(2R)247)
lethal | recessive
CG17683NC38, l(2)NC173NC173 has lethal phenotype
Separable from: a secondary lethal mutation.
Induced on: cn1 bw1.
l(2)NC173NC173/CG17683NC38 lethality due to a shared second site lethal.