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B
Chromosomal mutation
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C
Somatic mutation
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D
Gene mutation
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Solution
The correct option is C Somatic mutation
Point mutation is a genetic mutation where a single nucleotide base is changed, inserted or deleted from a sequence of DNA or RNA. Each triplet codon corresponds to an amino acid when translated to protein. When one of these codons is changed by a point mutation, the corresponding amino acid of the protein is changed.
Chromosomal mutation is presence or absence of one or more set of chromosomes in a cell or a structural abnormality in the normal set of chromosomes.
Somatic mutation is the occurrence of a mutation in the somatic cells (cells other than sperm and egg) of the organism. These are frequently caused by environmental factors like exposure to UV rays or to certain chemicals.
Gene mutation is a permanent alteration in the DNA sequence that makes up a gene. They are of two types: Hereditary mutations (inherited from parents) and Acquired mutation (occur at some time during a person's life).