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A frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a dna sequence that is not divisible by three. A frameshift mutation is a type of gene mutation in which the addition or deletion of one or more nucleotides causes a shift in the reading frame of the codons in the mrna, which may lead to the alteration in the amino acid sequence at protein translation. A frameshift mutation in a gene refers to the insertion or deletion of nucleotide bases in numbers that are not multiples of three
This is important because a cell reads a gene’s code in groups of three bases when making a protein. A dna sequence is a chain of many smaller molecules. A frameshift mutation is a type of genetic mutation resulting from the alteration of a number of nucleotides in dna sequences that are not multiple of three
Frameshift mutation occurs as a result of a change in the reading frame of the sequence.
A frameshift mutation is a genetic alteration resulting from the insertion or deletion of nucleotides in a dna sequence that is not a multiple of three. Frameshift mutations are insertions or deletions in the genome that are not in multiples of three nucleotides Frameshift mutation refers to the addition or deletion of nucleotides that alters the reading frame of the ribosome during translation, resulting in premature termination of the protein synthesis. A type of mutation in which a number of nucleotides deleted from or inserted into a protein coding sequence is not divisible by three, thereby causing an alteration in the reading frames of the entire coding sequence downstream of the mutation.
Learn how frameshift mutations disrupt the reading frame of a gene and why they often produce severely altered or nonfunctional proteins. A frameshift mutation is a genetic mutation caused by a deletion or insertion in a dna sequence that shifts the way the sequence is read
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