Explain point  mutations and frameshift mutations. Which is more apt to disrupt the  structure and or function of a protein coded for by a gene? Why?

Define coding and regulatory mutations and provide an example

What is mutations definition of mutations? types of mutations proper explanation and diagram

need help.  Which of the following are true in regards to the SARS-CoV-2 RNA-dependent RNA polymerase? Select all that apply It is an enzyme. It creates RNA polymers It copies the SARS-Cov-2 genome. It copies viral RNA that the host machinery then turns into proteins. It synthesizes DNA polymers. It breaks down RNA polymers It breaks down DNA polymers

.    Discuss    how    mutations    may    arise    in    DNA,    and    the    potential    consequences    for    gene    function    if    a    point    mutation    were    to    occur    in    (a)    the    coding    region    of    a    gene,    and    (b)    the    non-coding    regulatory    region    of    a    gene.

Which type of point mutation does not affect the resulting protein? a deletion b missense mutation c silent mutation d nonsense mutation

How might a point mutation in DNA affect the phenotype. How the genome is expressed in the organism? (Please explain this at the molecular level).

. Discuss what message does a gene provide? How is the language of the geneexpressed?

Answer completely and correctly: Why is it more likely that insertions or deletions will be more detrimental to a cell than point mutations?

Cystic fibrosis is a life-threatening disease that causes thick, sticky mucus to build up in areas of the body, including the lungs. Scientists are studying CFTR, the gene associated with cystic fibrosis in humans. In the majority of cystic fibrosis patients, the same mutation is seen in the same location on the CFTR geně. A partial DNA sequence, a partial MRNA transcript, and part of the normal polypetide that the makes up the CFTR protein that the CFTR gene codes for are shown in the diagram below. DNA 3 MRNA 5 AUC Polypeptide A partial DNA sequence, a partial MRNA transcript, and part of the CFTR polypeptide in a cystic fibrosis patient are shown in the diagram below. DNA 3 CACAA MRNA 5 Polypeptide Gly A Describe the change in the DNA sequence, the effect on the MRNA, and the effect on the polypeptide. B. Is this a "true" frameshift mutation? Why or why not? C. Would a single base insertion at the beginning of the gene have a larger or smaller effect on the resulting polypeptide…