Which of the following is mostly likely to result from an error during transcription A. it is formed by a particular sequence of amino acids B. it is read in groups of three nitrogenous bases C. it is made of the same components in all living organisms D. it is found in the base sequence of nucleic acids

So I think you're trying to ask where transcription errors take place, which I would say is A.

Explanation:

DNA transcrption is when DNA is converted to RNA, which is then sent to ribosomes in the cell to make specific protiens(this is how viruses destroy cells, they use this system to make more viruses by causing viral RNA or DNA(transcripted)to be given to ribosomes) Anyway, transcritpion makes certain sequences of Amino acids for protiens, so an error is going to affect this area first, which can cause large systematic problems later.

the best answer is, earth strong )

explanation:

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.