WebLitigation, Silent mutation, harmful mutation, beneficial mutation Amino Acid: Phenylalanine (PHE) UUC UUU Expert Answer 89% (9 ratings) Ans. Silent mutation. • A Change in mRNA nucleotide sequence from UUU to UUC results in a " silent mutation. " •silent mutation :- mutation that … View the full answer Previous question Next question WebQ. Mutations are only passed on to offspring when they happen in answer choices somatic cells gamete cells prokaryotic cells the mitochondria Question 9 30 seconds Q. If a mutation occurs in an expressed gene, it will most directly affect the structure of a cell's answer choices ATP proteins energy source membrane Question 10 30 seconds
silent mutation quizlet
WebApr 9, 2024 · Silent Changes After mutagen treatment, the vast majority of base pair changes (especially substitutions) have no effect on the phenotype. Often, this is because the change occurs in the DNA sequence of a non-coding region of the DNA, such as in inter-genic regions (between genes) or within an intron region. WebSilent mutations result in a new codon (a triplet nucleotide sequence in RNA) that codes for the same amino acid as the wild type codon in that position. In some silent mutations the codon codes for a different… Read More occurrence in mutation In mutation northfield exeter
Missense Mutations Flashcards Quizlet
WebMutation is a change in a gene or chromosome. It is a rare, random change in the genetic material, and in some cases it can be inherited. Causes of mutation Mutation can be spontaneous. It... WebSilent mutations are base substitutions that result in no change of the amino acid or amino acid functionality when the altered messenger RNA (mRNA) is translated. For example, if the codon AAA is altered to become AAG, the same amino acid – lysine – will be incorporated into the peptide chain. WebJun 23, 2024 · A silent mutation is a change in the sequence of nucleotide bases which constitutes DNA, without a subsequent change in the amino acid or the function of the overall protein. chemical changes in just one nucleotide (base pair) of a gene, A mutation that doesn't change the amino acid sequence, substitutions that change one amino acid … northfield experiment