Answer:
substitution - a base was changed
Explanation:
The nucleotide sequence CTT was changed to the sequence CAT. The T was substituted with an A. This changed the encoded amino acid from Glu to Val.
An insertion is where an additional base is added (e.g. if the sequence changed from CTT to CATT)
A deletion is when a base is lost (e.g. if the sequence changed from CTT to CT)
Answer:
Multiple Alleles.
Explanation:
Multiple Alleles. Alleles are alternative forms of a gene, and they are responsible for differences in phenotypic expression of a given trait.
Glad I could help.
So your answer seems like it is false
<span>Its location would be described as being at a particular locus on chromosome #2, perhaps in relation to the centromere or "on the short arm" of chromosome #2. If it is located on chromosome #2 in one fruit fly, that gene will also be on chromosome #2 of other fluit flies of the same species.</span>