C29745960T
L138F | IntS11-PA
L138F
Analogous mutation in human INTS11 implicated in neurodevelopmental disorder with impaired motor development and brain atrophy, INTS11-related; mutation carried on in vitro construct; site of nucleotide substitution in fly gene inferred by FlyBase curator based on reported amino acid change.
Variant protein coordinates based on the 606aa isoform (NP_001243385).