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Match the changed nucleotide sequences to the mutations that cause them.

Original Nucleotide Sequence: CATTCACACG

Changed Nucleotide Sequences:
1. CATTCACACA
2. CATTGCACAC
3. CATTGCACAC (again, if intentional)

\begin{tabular}{|l|l|l|}
\hline Type of Mutation & Original Nucleotide Sequence & Changed Nucleotide Sequence \\
\hline Deletion & CATTCACACG & \\
\hline Insertion & CATTCACACG & \\
\hline Inversion & CATTCACACG & \\
\hline Duplication & CATTCACACG & \\
\hline Substitution & CATTCACACG & \\
\hline
\end{tabular}


Sagot :

To match the given nucleotide sequences with the type of mutations, follow the categorization based on the results we have:

1. Original Nucleotide Sequence: CATTCACACG
2. Changed Nucleotide Sequences:
- CATTCACACA
- CATTGCACAC
- CATTGCACAC

Based on the analysis:

- CATTCACACA results from a substitution mutation.
- CATTGCACAC results from a substitution mutation.
- CATTGCACAC results from a substitution mutation. (It is repeated but it's the same mutation.)

Now we can categorize them in the table:

\begin{tabular}{|l|l|l|}
\hline
Type of Mutation & \begin{tabular}{l}
Original Nucleotide \\
Sequence
\end{tabular} & \begin{tabular}{c}
Changed Nucleotide \\
Sequence
\end{tabular} \\
\hline
deletion & CATTCACACG & \\
\hline
insertion & CATTCACACG & \\
\hline
inversion & CATTCACACG & \\
\hline
duplication & CATTCACACG & \\
\hline
substitution & CATTCACACG & CATTCACACA \\
\hline
substitution & CATTCACACG & CATTGCACAC \\
\hline
substitution & CATTCACACG & CATTGCACAC \\
\hline
\end{tabular}

This is how the changed nucleotide sequences match with the types of mutations that caused them.