loss of function allele
amorphic allele - genetic evidence
Nucleotide substitution: A778T, transversion event.
A14616339T
A778T
M1L | Adh-PC; M1L | Adh-PE; M1L | Adh-PF; M1L | Adh-PH; M1L | Adh-PI
Mutation of the start codon; induced on an AdhF chromosome.
electrophoretic variant
Sofer.
Selected as: Pentenol resistant larva.
CRM negative.
CRM negative.