hypomorphic allele - genetic evidence
Nucleotide substitution: T-1388G. Nucleotide -1386 (T) is deleted (coordinates as in FBrf0046390), this results in a frameshift.
T-->C at -1388 and deletion of T at -1386 generating frameshift and TGA stop codon two codons downstream
Deletion of one base, causing a frameshift. Second of two lesions in ry5204 mutant.
T13032785G
T1388G
V7G | ry-PA
One of two lesions associated with ry5204 mutation.
McCarron.