The base-pair deletion dna mutations is the most likely to be damaging to the protein it specifies.
A mutation is a change in an organism's DNA sequence. Mutations can occur as a result of mistakes in DNA replication during cell division, mutagen exposure, or viral infection. Cystic fibrosis, hemophilia, and sickle cell disease are all caused by hereditary mutations. Other mutations can occur on their own during a person's life. These are referred to as sporadic, spontaneous, or novel mutations. They only have an effect on a subset of cells. In gametes, germline mutations arise. Other cells in the body experience somatic mutations. Chromosomal changes are mutations that modify the structure of the chromosome. Point mutations affect only one nucleotide.
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