Nucleotide substitution: C?T.
Amino acid replacement: Q492term.
C23793812T
C?T
Q492term | mbc-PA; Q492term | mbc-PB
Q492term
nucleotide position inferred by curator based on amino acid change reported in FBrf0094649; mutations characterized in FBrf0094649 are reported to be GC to AT transitions at single nucleotides
Severe somatic muscle phenotype. Defects in midgut constriction and orientation. Overall structure of the heart is normal. Defects in dorsal closure and cytoskeletal organisation in the migrating epidermis.