Amino acid replacement: F579Y.
The F579Y amino acid replacement in Dhc64C is equivalent to a F582Y change in the orthologous human DYNC1H1 gene, which corresponds to the Loa mutation in the mouse ortholog (this mutation results in neurodegeneration in mice).
T4822554A
T?A
F576Y | Dhc64C-PA; F576Y | Dhc64C-PC; F576Y | Dhc64C-PD; F576Y | Dhc64C-PE; F576Y | Dhc64C-PF; F576Y | Dhc64C-PG; F576Y | Dhc64C-PH; F576Y | Dhc64C-PI
F579Y
Mutated nucleotide determined from oligo sequence. Mapped to F576 rather than F579 as reported.