Nucleotide substitution: G-1366A (coordinates as in FBrf0046390). This may cause a splicing defect.
G --> A at -1366 (AAG-->AAA) (alters splice efficiency at exon 1/intron 1 junction)
G13032807A
G1366A
K14K | ry-PA
The silent G to A nucleotide change in the K14 codon is thought to cause a splicing defect.
McCarron.