Which of the Following Is Never a Frameshift Mutation

The engaging quiz is interactive and it can give you instant results. S that are necessary for cell specialization.

Mutations Microbiology

B The mutation results in the same amino acid in the protein.

. Frameshift mutations have a more dramatic effect on the polypeptide. Which of the following mutations is likely to cause the most dramatic phenotypic change. Since codons are read in groups of 3 an insertion of 3 or 6 would not cause a shift in the positions of all subsequent nucleotides.

A frameshift mutation one codon away from the 3 end of the nontemplate strand Answer. The resulting protein will be too short and non-functional. A highly recurrent frameshift mutation of MLL2 was identified in cancer tissues and this type of frameshift mutation of MLL2 is predicted to induce nonsense.

Deletions duplications inversions and translocations all of the above could be described as a chromosomal mutation. Is it possible to have a mutation but keep the same number of bases and the same base composition. Insertions involve the insertion of one of more extra nucleotides into a DNA chain.

A frameshift mutation completely changes the genetic code from the point of the mutation so the protein made as a result of the mutation would have the incorrect structure and would not function. To see more answers head over to College Study Guides. UAC CGG GUU AGU ACU.

The phenotype will change but not the genotype. In this particular type of indel mutations the number of nucleotides mutated is fairly low there may be very limited effect on protein function as well Related Biology Terms A-site of Ribosome The ribosomal site that mostly receives an incoming tRNA charged with an amino acid residue. The resulting protein will not be affected.

What does this figure represent. Gene Mutation D NA Repair and Transposition Of the following types of mutations which will not be passed to offspring. 3 In a frameshift mutation.

If a frameshift mutation causes a stop codon to be inserted into the DNA sequence. 4 A change in a cells DNA sequence is. Several diseases have frameshift mutations like HIV Crohns disease cystic fibrosis etc.

Choice A A Genes encode molecule. C The mutation results in all codons changed downstream. A a base insertion only B a base deletion only C a base substitution only.

Which of the following is NEVER a frameshift mutation. Each group of three bases corresponds to one of 20 different amino. Transcription in this case will result in.

A The mutation results in a different amino acid in the protein. Which of the following is most likely to cause a. THIS SET IS OFTEN IN FOLDERS WITH.

If a frameshift mutation occurs then the mRNA codons will code for different amino acids. Which of the following is NOT a gene mutation. Since amino acids make up proteins the resulting protein will not function properly or not function at all.

The question contains content related to Biology and Science. Which of the following is NEVER a frameshift mutation. A frameshift mutation is a mutation caused by an insertion or deletion which causes a shift in the translational reading frame.

Added 1282015 15052 AM This answer has been confirmed as correct and helpful. The following quiz will help you master the effects of frameshift mutations. Averys experiments showed that bacteria are transformed by A.

Due to a point mutation transcription results in the mRNA sequence of. Hox genes determine an animals A. This 23 words question was answered by Jared M.

Divisible by three is important because the cell reads a gene in groups of three bases. The original DNA has the following sequence of nitrogen bases. A frameshift mutation can result from the addition of a nucleotide to a sequence.

Which of the following best describe how genes allow cells to carry out essential life functions. A frameshift mutation is a type of mutation involving the insertion or deletion of a nucleotide in which the number of deleted base pairs is not divisible by three. On StudySoup on 5312017.

There are two types of frameshift mutationsThey are insertions and deletions. Which of the following is most likely to cause a frameshift mutation. A frameshift mutation could result from _____.

Which of the following is NEVER a frameshift mutation. D The mutation results in a stop codon. A frameshift mutation can result from a deletion of a nucleotide to a sequence.

RNA contains the sugar. Which of the following is NEVER a frameshift mutation. A frameshift mutation can result from the deletion of three nucleotides from a sequence.

Choice B B Genes can code for nucleotides which help to determine the specialized roles of organelles in the cell. A a duplication of all or most introns. During transcription an RNA molecule is formed.

ATG GCC CAA TCG TGA. RNA contains the sugar. There is no frameshift mutation.

It usually only changes one amino acid in the protein coded for by a gene. Substitution is never a framshift mutation.

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