<span>The correct answer is A) a single amino acid may have more than one codon that translates for it.</span>
<span>This property of the codon is called codon degeneracy and is the redundancy of the genetic code. As a result, there is the multiplicity of three-base-pair codon combinations that specify an amino acid and that increases tolerance to point mutations (synonymous mutations). Usually, the codons encoding one amino acid differ in the second or third position.</span>
I think it’s number 2 but I could be wrong, I know 1,3, and maybe 4 are in living things
Metaphase 1 is when <span>tetrads of homologous pairs lined up along the center of the cell and attached to the spindle fibers in meiosis. Hope I helped!</span>
The cross of heterozygous
AaBb as parental phenotype led to formation of 1
6 phenotype of the offspring.This is because this is dihybrid form of inheritance .The probability of having
aabb offspring is
1/16 since there is only one aabb type of offspring phenotype out of
the
16. An illustration of how crossing is done is as per punnet square below
