What are color blindness genetic chromosome mutation?

Color blindness is primarily caused by genetic mutations affecting the photopigments in the cone cells of the retina, which are responsible for color perception. Most commonly, these mutations occur on the X chromosome, making color blindness more prevalent in males, who have only one X chromosome. The most common forms include red-green color blindness, which results from mutations in the genes that encode photopigments sensitive to red and green light. Other types, like blue-yellow color blindness, involve different genetic factors but are less common.