How is it possible that over 20 million living organisms on the planet are made up of only 5 types of nucleotide bases arranged in long chains

There are only five types of nucleotide basis are present in the genetic material which makes up the all the genetic information of the individuals. These nucleotides are named as Adenine, Thymine, Guanine, Cytosine and Uracil. In all the living beings on the earth, these only five nucleotides are present which decides their behavior and functions on the earth. These five bases have features to get any arrangements according to the situation. Their different arrangement at the heredity material makes the difference in all living beings regarding their behavior.

answer: 21

step-by-step explanation:

divide 630 by 30. 30 goes into 630 21 times

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.