Answer: Option A) Yes, the 5th amino acid in the sequence has changed.
Explanation:
Absolutely, the change of CCG to CAG does cause the amino acid Proline to be substituted by Glutamine.
Thus, the single base change of cytosine to adenine in CCG and CAG resulted in a different protein.
The genealogy tree which is missing from the question is in the attachment.
Answer: 1) P1 =
; 2) P2 =
; 3)P3 = 
Explanation: 1) According to the genealogy tree, the individual III-3 has a P1 = 1/2, because each of the parents are heterozygous for the condition, since one of the ofspring is affected.
2) For individual III-4, one of the parents is heterozygous for the condition, so the probability of being a carrier is P2 = 1/2.
3) Now, for individual IV-1 be affected, the parents has to be carrier. So, this probability, depends on the probability of each parent being heterozygous and that the individual will be carrying the condition, which means:
P3 = 1/2 · 1/2 · 1/4 = 1/16.
The probability of having the condition is 1/16 or 6.25%.
Answer: 3/4 of the offspring will have a phenotype resembling the parent with the genotype AABBCc.
Explanation:
This is because out of the eight possible chances, six of them have a physically observable trait similar to the AABBCc genotype.
Answer:
Does not have a specific shape
Explanation:
Irregular galaxies are just that: irregular. They don't have a single common shape. Irregular galaxies are among the smallest galaxies