Mutation ( that’s what I put )
<span>Point mutations are of two types: Substitutions of bases that are the change of one base of DNA by another. And Transitions that are replaced on a pyrrhic basis by another pyrrhic or a pyrimidine by another pyrimidine. Transversions: substitution of a pyrrhic base by another pyrimidine or vice versa. These mutations are negative because they affect only one of the nucleotides, and therefore, only one triplet of bases are affected. When the mutation does not affect the individual it is a silent mutation. Chromosomal mutations Changes in the structure of the diploid chromosomes, where one of the chromosomes has a mutation, will have another normal. They can hinder the process of meiosis in the carrier since it hinders the correct pairing of the homologous chromosomes. It would produce an unfeasible offspring or with mutations.</span>
Humans have 22 chromosome pairs and two sex chromosomes. Females have two X chromosomes; males have an X chromosome and a Y chromosome. ... In humans, animals, and plants, most chromosomes are arranged in pairs within the nucleus of a cell. Humans have 22 of these chromosome pairs, called autosomes.
The polar nuclei of the center cell
Answer:
The answer is c I think sorry if it is wrong
