deletion mutation
Point mutation and it can be effective or silent depend upon at the site of codon
Point Mutation is the mutation that involves a single or few nucleotide. This type of mutation replaces a single nucleotide to another.
Point Mutation- a type of gene mutation in which only a single nucleotide in a gene has been changed.
A substitution mutation is a type of genetic mutation where one nucleotide in the DNA sequence is replaced with a different nucleotide. This can lead to changes in the amino acid sequence during protein synthesis, potentially altering the function of the protein. The impact of a substitution mutation on the genetic code depends on where it occurs and what specific nucleotide is substituted.
A deletion mutation occurs when a nucleotide is dropped from a DNA sequence. This can cause a shift in the reading frame, leading to a non-functional protein being produced.
If one nucleotide is replaced by another, it is called a point mutation. This type of mutation involves a change in a single nucleotide within the DNA sequence.
deletion
Substitution
This type of mutation is called a missense mutation. It can lead to a change in the protein or enzyme's structure and function, possibly affecting its biological activity. The impact of the mutation can vary depending on the specific amino acid substitution and its location within the protein.
This is a substitution mutation where the nucleotide "c" is replaced with "g" at the beginning of the sequence.
Yes, substitution is a type of gene mutation where one nucleotide is replaced by another in the DNA sequence.
A frame-shift mutation.