Answer:
Genetic variation is a term used to describe the variation in the DNA sequence in each of our genomes. ... Individuals of a species have similar characteristics but they are rarely identical, the difference between them is called variation
Explanation:
Explanation:
<u>C. A red allele is present on both homologous chromosomes</u>
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Homologous chromosomes are pairs of chromosome of similar lengths, banding patterns, and centromere positions, with genes at the same loci. For dominance, gene copies are present on both of the chromosomes; the dominat variant overrides the effect of the other recessive allele.
Further Explanation:
DNA molecules contain chromosomes that may have different forms called alleles. DNA, which is the genotype, is transcribed into mRNA and later translated into amino acids which are connected together by rRNA to form proteins which constitute the phenotype of an organism. DNA sequence mutations form new alleles, impacting the associated mRNA, and thus the encoded protein.
Homozygous individuals have a chromosome containing two variants of the same allele. Dominant homozygous individuals bear two copies of the dominant allele, whereas recessive homozygous individuals hold two copies of the recessive allele.
Learn more about mutations at brainly.com/question/4602376
Learn more about DNA and RNA at brainly.com/question/2416343?source=aid8411316
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Answer: An inherited trait that makes an individual different from other members of its species is called a variation.
