One of the parents of a cross has mutation in its mitochondria. In that cross, that parent is taken as a male. During segregation of F2 progenies that mutation is found in

Question

$\begin{array}{1 1} \text{a. One third of the progenies.} \\ \text{ b.None of the progenies} \\ \text{c. All of the progenies} \\ \text{d. Fifty percent of the progenies.} \end{array} $