Amino acid replacement: P51L.
The progenitor P{EP}Mkp311 insertion is still present on the chromosome.
Nucleotide substitution: C?T.
C19085572T
C?T
P51L | Mkp3-PB; P51L | Mkp3-PC; P51L | Mkp3-PD
P51L
Selected as: a revertant of the phenotype caused by overexpression from the P{EP}Mkp311 insertion.