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A hereditary mutation is a change in the DNA sequence that is passed from parents to their offspring through reproductive cells (sperm and eggs). These mutations can be inherited in various patterns, such as autosomal dominant or recessive, and can affect traits or predispose individuals to certain diseases. Unlike somatic mutations, which occur in non-reproductive cells and are not passed on, hereditary mutations can be present in every cell of an individual and may influence their health and development throughout their life.
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What is the difference between an acquired mutation and a hereditary mutation?
An acquired mutation, also known as a somatic mutation, occurs in an individual's cells during their lifetime and is not passed to offspring. These mutations can result from environmental factors, such as radiation or chemicals, or errors during cell division. In contrast, a hereditary mutation is present in the germline cells and can be inherited from a parent, affecting all cells of the offspring. This type of mutation can be passed down through generations and is often associated with genetic disorders.
What is a permanent heritable change in an allele that produces a different variant of the same trait?
A permanent heritable change in an allele that produces a different variant of the same trait is called a mutation. Mutations can lead to genetic diversity within a population and are the raw material for evolution.
What is the opposite of somatic mutation?
The opposite of a somatic mutation is a germline mutation. While somatic mutations occur in non-reproductive cells and are not passed on to offspring, germline mutations occur in the reproductive cells and can be inherited by future generations. These mutations can affect the entire organism and can lead to hereditary conditions.
What is a gene mutation?
Gene mutation is the change in the DNA sequence that is permanent and leads to new genetic traits and even diseases. This type of mutation is triggered through hereditary process or through several factors in the environment.
What are the causes of hereditary fructose intolerance?
Fructose intolerance is an inherited disorder passed on to children through their parents' genes. Both the mother and father have the gene that causes the condition, but may not have symptoms of fructose intolerance themselves.
What are the forms of mutation?
== ==mutation means:change in a hereditary character
What does mutation?
mutation means: change in a hereditary character
What changes in a mutation?
hereditary instructions
What is changes in hereditary material called?
It is called a mutation.
What do you call a change in the hereditary instructions of an organism?
A change in the hereditary instructions of an organism is called a mutation. Mutations can occur randomly or be induced by factors such as UV radiation or chemicals, leading to variations in the organism's traits.
Is sickle cell anemia a point mutation?
An example of point-mutation is sickle-cell anemia. Sickle-cell disease is hereditary.
What is the type of mutation that causes deafness?
that would be a hereditary thing not a gene mutaion
Sickle-cell anemia is an example of a point-mutation?
An example of point-mutation is sickle-cell anemia. Sickle-cell disease is hereditary.
How can a baby be born with out a hand?
hereditary or a mutation due to a mothers use of drugs and or alcohol.
What is the difference between an acquired mutation and a hereditary mutation?
An acquired mutation, also known as a somatic mutation, occurs in an individual's cells during their lifetime and is not passed to offspring. These mutations can result from environmental factors, such as radiation or chemicals, or errors during cell division. In contrast, a hereditary mutation is present in the germline cells and can be inherited from a parent, affecting all cells of the offspring. This type of mutation can be passed down through generations and is often associated with genetic disorders.
Can cytoplasmic mutation be transmitted from parents to their child?
only the hereditary character can be transmitted and it is found in nucleus not in cytoplasm so the cytoplasmic mutation can not be transmitted from parents to their child. hope u get the answer
What is a permanent heritable change in an allele that produces a different variant of the same trait?
A permanent heritable change in an allele that produces a different variant of the same trait is called a mutation. Mutations can lead to genetic diversity within a population and are the raw material for evolution.
