Answer:
Its a substitution mutation because one of the specific base, G is replaced by A.
This is a Point Mutation because Point mutation brings changes in the structure of a gene because of the substitutions with another base pair. Like in this case, G is substituted by A. In case of frameshift mutations, there is a change in the number of nucleotides due to either insertions or deletions of the nucleotides, which is not in this case.
Answer:
Both parents are heterozygous carriers.
Explanation:
Both parents are heterozygous carriers. Sickle Cell Anaemia is usually referred to as a recessive condition since an individual must have two copies of the sickle gene in order to have the disorder.
Since neither of the parents is ill, both of them must be heterozygous carriers for the child to have the disorder
I can't really give you a percentage sorry. My answer is Possible, yes but probable, no.
Man i hate school that really makes my head hurt
Yoyr muscles will switch to anaerobic respiration and produce lactic acid
