Answer:
Its D mitochondria
Explanation:
lol i learned about cells for a longggg time so i know this
Hi,
If a point mutation occurs during which CGA changes to AGA, the mutation will be simply inherited to the offspring and there won't be any harsh effects on the health of individual.
This is because, both AGA and CGA code for same amino acid called Arginine.
We know that mutations posses harmful effects when they change the genetic sequence leading to the incorporation of incorrect amino acid in the organisms and their offspring. But in this case the mutation will not be harmful and will simply be transferred to the offspring and will have no effect on the functioning, fitness or survival of the organism
Hope it helps!:)
In gametes generated by F1 tri-hybrids and gametes produced by parents from true-breeding populations.
When non-sister chromatids of homologous chromosomes exchange genetic material during meiosis, novel allelic combinations are created in the daughter cells. The locations of three genes in the genome of an organism are identified using a three-point cross. A homozygous recessive individual is crossed with a person who is heterozygous for three mutations, and the progeny's phenotypes are graded. When F1 progeny are self-pollinated, a 3:1 ratio of F2 progeny are created.
To konw more about homologous chromosomes please click on the link brainly.com/question/27258467
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