A deletion causing a frame shift mutation.
A frame-shift mutation.
A frame shift mutation destroys the correct sequence of amino acids from the point of the mutation. The protein produced by a frame shift mutation would more than likely be nonfunctional.
This is called an insertion mutation.Some repeats, such as the repeats in the Huntington's gene, can be repeated too many times and then you have the deleterious mutation in this gene.
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Substitution is not ever a frame shift mutation. However, insertion, point mutation, and deletion are all examples of a frame shift mutation.
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"I believe there is insertion and deletion, (one kind), and substitutions. (the second kind)" This answer is incorrect, the two types of frameshift mutation are insertion and deletion, these both alter the translation reading frame. A substitution point mutation in DNA is referred to as a single-nucleotide polymorphism and does not result in any change to the translational reading frame. insections and deletions are two types of frameshift mutations
Point Mutations always result in [causing] a frame-shift mutation so they are the same.
Adding or subtracting just one nucleotide would cause a frame shift mutation.
A point mutation that does not produce a frame shift is when one single base is replaced by a different base. This changes the DNA sequence, but does not cause a frame shift because it is a switch not an addition or subtraction of a base.
A deletion causing a frame shift mutation.
When a addition or deletion mutation occurs, changing the reading frame.
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true
No
A frame-shift mutation.