Answer:
A frameshift mutation can be described as a genetic mutation in which a single nucleotide or more than one nucleotide is inserted or deleted from the sequence of the DNA. As the gene expresses itself in the form of triplets of a genetic code, insertion or deletion can cause devastating changes in the genetic code due to which wrong proteins will be synthesized.
Frameshift mutations can be more noticeable than the substitution mutation. In a substitution mutation, only one of the nucleotides is shifted with another. The entire genetic code is not affected by it.
Answer:
The answer is B
Explanation:
I know it's B because I did this question before.
hope this helps :)
People with two copies of the sickle cell gene have the disease. People who carry only one copy of the sickle cell gene do not have the disease, but may pass the gene on to their children. Abnormal hemoglobin, called hemoglobin S, causes sickle cell disease (SCD). The problem in hemoglobin S is caused by a small defect in the gene that directs the production of the beta globin part of hemoglobin. This small defect in the beta globin gene causes a problem in the beta globin part of hemoglobin, changing the way that hemoglobin works.
