I don't really know what this question is asking but I'm just gonna list what I know...
Colour blindness is an X-linked recessive disorder. This means that the father's genotype will be
while the daughter's genotype will be
as she will automatically receive the recessive allele from dad and the fact that she isn't colourblind means that she received the dominant allele from mom.
If this woman is married to a man with with a genotype of
, then there is a 50/50 chance that a boy will be colourblind and no chance that a girl will be colourblind but there is a 50/50 chance that she will be a carrier.
If married to a man with a genotype of
, then there is a 50/50 chance that a boy will be colourblind, and a 50/50 chance that a girl will be colourblind but there is a 50/50 chance that she will be a carrier.