Amino acid replacement: P760L.
The mutation is equivalent to a P742L change in the orthologous human CYFIP1 gene, a variant identified in patients with a severe neurodevelopmental disorder.
C15335792T
P760L | Cyfip-PA
P760L
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 CyfipI471V)
viable (with CyfipI471V)
axon | adult stage (with CyfipI471V)