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Name Class Section 12 4 Mutations pages 307 308 Key Concept What are mutations Introduction page 307 2. Is the following sentence true or false Chromosomal mutations result from changes in a single gene. Kinds of Mutations 3. Mutations that occur at a single point in the DNA sequence are mutations. 4. A mutation involving the insertion or deletion of a nucleotide is a an 5. Complete the table of types of chromosomal mutations. CHROMOSOMAL MUTATIONS Type Description Examples ABC DEF AC DEF Duplication Part of a chromosome becomes oriented in the reverse of its usual direction Translocation Pearson Education Inc* publishing as Pearson Prentice Hall* 6. Circle the letter of each sentence that is true about gene mutations. a* Point mutations affect just one nucleotide. b. The substitution of one nucleotide for another in the gene never affects the function of the protein* reading frame of the genetic message. d. Frameshift mutations affect every amino acid that follows the point of the mut....

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  6. Determine whether the statement about chromosomal mutations is true or false, as this will gauge your understanding of the material.
  7. For the 'Kinds of Mutations' section, identify the types of mutations by filling in the answers based on your understanding of genetic principles.
  8. Complete the table detailing types of chromosomal mutations. Make sure to include descriptions and examples accurately.
  9. Address the statements about gene mutations, circling the correct letters for those that are true.
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Any sudden heritable change is called mutation. Gene mutations are the changes that occur in one or more genes that can lead to harmful diseases or illnesses. Genes can be defined as small portions of the DNA, knob like and present in a single linear row over the chromosomes.

This means that typically every child has around 60 to 70 new mutations that their biological parents don't have. These mutations are responsible for genetic variation along with many genetic diseases.

Do Parents Pass Gene Mutations to Children? If a parent carries a gene mutation in their egg or sperm, it can pass to their child. These hereditary (or inherited) mutations are in almost every cell of the person's body throughout their life.

This means that a human genome accumulates around 64 new mutations per generation because each full generation involves a number of cell divisions to generate gametes.

Mutations can be of many types, such as substitution, deletion, insertion, and translocation.

We call this mode of inheritance “recessive”. Unlike with dominant conditions, the parents of a child with a recessive disease will not show signs of the disease.

Can I inherit genetic mutations? Yes, you can inherit germline genetic mutations, while somatic mutations occur with no previous history of the mutation in your family. There are several patterns that genetic mutations can pass from the parent to a child (hereditary).

There are three types of DNA Mutations: base substitutions, deletions and insertions.

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