That's correct - it's a square where on one axis, the paternal allele (allele = one of the possible forms of the same gene), and on another the maternal allele is listed. Often, it's also indicated whether an allele is recessive or dominant.
Then, in the table that results, all the possible "combinations" of allele between the paternal and maternal party are created. If you count how often a certain combination appears, it indicates the likelihood of that combination.
See the picture (though it is directly from Wikipedia, please note). The likelihood of BB is 25%, of Bb is 50%, and of bb 25%.
Explanation:
A frameshift mutation is an insertion or deletion in a sequence of DNA which disrupts the way the code is read. It occurs when the codons undergo a disruption through the deletion or insertion of one or multiple nucleotides (given that the number removed or added are not multiples of 3) - this alters the open reading frame; the amino acids produced through translation simply occur in a different sequence.
Further Explanation:
During the process of cell division, spontaneous changes within the genome can arise. These mutations are errors occur when copies of the DNA within the cell are made; mutations may range from small changes called single nucleotide polymorphisms, to large scale deletions, and additions which span multiple genes. There are two types:
- somatic: these only occur within certain cells, and arise from environmental factors such as UV light
- hereditary: occur within germ cells of the parent and later the fertilized egg which forms a zygote; these are present within all cells of the new organism.
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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Which of what? I need more information to decipher that.