Answer:
A scatter plot shows all of those
Explanation:
Answer:
Deletion in a nearby gene, chromosome breakage, and translocation of the gene to a heterochromatic location.
Explanation:
Transposable components (TEs), also known as "jumping genes," are DNA sequences that moves starting with one area on the genome then onto the next, in some cases making or reversing mutation and changing the cell's hereditary character and genome size.
At the point when the transposon is extracted from the original site, it may remove a portion of the gene sections alongside it. This prompts the presence of a serious phenotype. Transposable components can likewise cause chromosome breakage. On the off chance that the whole gene is moved alongside the transposon to a heterochromatic location, the gene gets silenced
Answer:
Homozygous recessive
Explanation:
The parents of the individual displaying the sickle cell anemia (SS) are phenotypically normal parents meaning, both parents are carriers of the (AS) gene which is a recessive trait for sickle cell anemia.
The individual took up the SS allele from both parents which makes him/her homozygous recessive. An individual is said to be homozygous recessive if that individual carries two copies of the same recessive allele.
Homozygous dominant is when an individual carries two copies of the same dominant allele (e.g AA).
