The disease caused by a uncontrolled division of abnormal cells in a part of the body!
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<span>Polydactyly in its most common form, is an autosomal dominant mutation. Let's represent the mutation as P and the normal state as +. Thus, if both parents are heterozygous (P+), both would have the mutation (and thus have six fingered). They have 3/4 chances of having a child with the extra digit, 1/4 normal. </span>
Answer:
b. Even though the DNA sequence changed, the sequence still codes for the same amino acid, so no change in phenotype will occur.
Explanation:
There is redundancy in the genetic code. That means that different codons can code for the same amino acids, so some mutations do not change the amino acid sequence of the protein.
Here, the amino acid is unchanged with the mutation.
If the amino acid sequence of the protein is the same, then the protein is not changed, so there will be no change in the phenotype
Answer:
a) epigenetic change.
Explanation:
Epigenetic is referred to changes BESIDES the changes in the genetic changes. It means, not related to mutations but to chemical changes such as methylation, acetylation, ubiquitylation, phosphorylation, that can interfere with the genetic expression. Chromatin modification is another way of epigenetic change.
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