Amino acid replacement: I471V.
The mutation is equivalent to a I476V change in the orthologous human CYFIP1 gene, a variant identified in patients with a severe neurodevelopmental disorder.
A15334869G
I471V | Cyfip-PA
I471V
Analogous mutation in human CYFIP1 implicated in neurodevelopmental disorder, CYFIP1-related; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.
fertile (with CyfipP760L)
viable (with CyfipP760L)
axon | adult stage (with CyfipP760L)