What’s the difference between frameshift mutations and point mutations

Answer:

Mispairing of DNA molecule causes the Frameshift mutations, changes in single base pair nucleotide sequence usually insertion or deletion results in these mutations. Point mutations occur when a single nucleotide is replaced with another nucleotide base.

The whole information coded in the amino acid changes due to a Mutation occurs in the sequence of DNA molecule in a frameshift mutation. The mutation occurs in the sequence of a DNA molecule.

Gene mutation Chromosomal mutation

It is a change in nucleotide sequence, in a particular gene. It is a change in several genes, in the chromosome.

Gene mutation is an only slight structural

Explanation:

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The two forms of gene mutations that may result from mistakes in DNA replication and mutagens are point mutations and frameshift mutations. Gene mutations are minor changes that take place in a gene's nucleotide sequence.

The primary distinction between a point mutation and a frameshift mutation is that a point mutation only affects one nucleotide in a gene, whereas a frameshift mutation affects one or more nucleotides and changes the open reading frame of a specific gene. Point mutations are primarily nucleotide substitutions that result in silent, missense, or nonsense mutations. Nucleotide insertion or deletion causes frameshift mutations.

A single nucleotide in DNA may change in a point mutation. The severity of this mutation is often lower than that of a chromosomal change.

A frameshift mutation occurs when one or more nucleotides are deleted or added, changing the base sequence's reading frame.

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