Okay, here's the information about the given DNA sequence alteration, formatted in Markdown with the specified linking convention:
This change represents a mutation in the DNA sequence. Specifically, the sequence "TAGCTGA" has been altered to "TAGTGA". This alteration involves the deletion of a single nucleotide, "C", from the original sequence.
This type of mutation is called a deletion. Deletions can have a range of effects, depending on where they occur in the genome and how many nucleotides are deleted.
If the deletion occurs within a gene, it can lead to a frameshift%20mutation if the number of deleted bases is not a multiple of three. A frameshift mutation will change the reading frame, leading to a completely different amino acid sequence from the point of deletion onward. This will likely produce a non-functional protein.
If the deletion results in a number of deleted bases that is a multiple of three, the reading frame is preserved. However, this can still result in the loss of one or more amino acids which can affect protein%20function.
If the deletion occurs in a non-coding region of the DNA, it may have little or no effect. However, some non-coding regions are important for regulation, so a deletion in those regions could potentially affect gene expression. This change can be referred to as a point%20mutation.
The significance of this specific deletion ("TAGCTGA" to "TAGTGA") would depend on its location and the context of the surrounding DNA.
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