How are mutations and genetic code related?

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(N/A) Mutation is defined as a sudden inheritable change in the genetic material.
It is categorized into the following types:
$(i)$ Point mutation: This involves a change in a single base pair where one base is replaced by another. $A$ classical example is the change of a single base pair in the gene for the $\beta$-globin chain,which results in the substitution of the amino acid glutamate with valine. This leads to a condition known as sickle cell anemia.
$(ii)$ Frameshift mutation: This is a change in the reading frame of the genetic code due to the insertion or deletion of base pairs.
$(a)$ Insertion: If one or more nucleotides are added to the $DNA$ segment,it is called insertion. If three or a multiple of three bases are added,the reading frame remains unchanged,but a protein with additional amino acids is formed.
$(b)$ Deletion: If one or more nucleotides are removed from the $DNA$ segment,it is called deletion. Similarly,if three or a multiple of three bases are removed,one or more amino acids are deleted from the polypeptide chain.

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Similar Questions

Which triplet codon acts as a stop signal for the process of translation?

Find out the incorrect match.

How many base additions or deletions do not change the reading frame?

During protein synthesis in an organism,the process stops at a certain point. Select the set of codons from the following that can terminate this process.

Match the codons given in column $I$ with their respective amino acids given in column $II$ and choose the correct answer.
Column $I$ (Codons)Column $II$ (Amino acids)
$(A)$ $UUU$$(I)$ Serine
$(B)$ $GGG$$(II)$ Methionine
$(C)$ $UCU$$(III)$ Phenylalanine
$(D)$ $CCC$$(IV)$ Glycine
$(E)$ $AUG$$(V)$ Proline

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