Nucleotide substitution: G?A.
The premature stop codon is at position 48 in the homeobox.
Amino acid replacement: W237term.
G26877605A
G?A
W238term | ro-PA; W238term | ro-PB
W238term
TGG to TAG; ro237B is reported as a nonsense mutation in which a 237aa translation product is produced.
Rough eye phenotype.
Strong ro allele.