A mutation can alter the sequence of DNA, causing changes in the mRNA produced during transcription. This can result in the insertion, deletion, or substitution of amino acids in the protein sequence during translation. These changes can impact the structure and function of the protein, potentially leading to a non-functional or altered protein being produced.
A third deletion could restore normal function if it results in a frameshift that re-aligns the reading frame back to its original state. For instance, if the first two deletions caused a shift, the third deletion might eliminate a subsequent nucleotide that ensures the reading frame is corrected. Additionally, if the deletions occur in a way that the remaining sequence can still produce a functional protein or if the deleted nucleotides were non-essential for protein synthesis, normal function might be reinstated. However, this is highly dependent on the specific context of the deletions and the gene involved.
A point mutation is when 1 base pair is swapped out for another one... so instead of an A you might find a C... or T... or G. Also an insertion or deletion of a base pair A mutation of a single point :)
Deletion (resulting in a frame shift), duplication (also resulting in a frame shift), or a plain old SNP (change of base). You might also be looking for one which changes the amino acid coding sequence and one that does not.
It's not ACCTGGAT.I think it might be TGGACCTA.you are wrong.. it IS ACCTGGAT
The protein might be unable to function.
A mutation can alter the sequence of DNA, causing changes in the mRNA produced during transcription. This can result in the insertion, deletion, or substitution of amino acids in the protein sequence during translation. These changes can impact the structure and function of the protein, potentially leading to a non-functional or altered protein being produced.
The whole program might face Deletion. This is one of many examples for sentence use..
A third deletion could restore normal function if it results in a frameshift that re-aligns the reading frame back to its original state. For instance, if the first two deletions caused a shift, the third deletion might eliminate a subsequent nucleotide that ensures the reading frame is corrected. Additionally, if the deletions occur in a way that the remaining sequence can still produce a functional protein or if the deleted nucleotides were non-essential for protein synthesis, normal function might be reinstated. However, this is highly dependent on the specific context of the deletions and the gene involved.
A point mutation is when 1 base pair is swapped out for another one... so instead of an A you might find a C... or T... or G. Also an insertion or deletion of a base pair A mutation of a single point :)
Deletion (resulting in a frame shift), duplication (also resulting in a frame shift), or a plain old SNP (change of base). You might also be looking for one which changes the amino acid coding sequence and one that does not.
A single number, such as 29513101917, does not provide any information as to what the sequence might be.
You might be going for the word sequence.
"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
For a start you might want to go to NFS World Support, or by contacting the Admins for a account deletion of the recent account.
um i don't know did u check your book? sometime your book might give you a better answer than on-line because on-line might be wrong.. I'm sorry hoped this helps a little
It's not ACCTGGAT.I think it might be TGGACCTA.you are wrong.. it IS ACCTGGAT