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A substitution mutation in genetics is where one of the nucleotide bases of DNA is swapped for another. These mutations may or may not affect the protein that is being coded.

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What is the name for a change in DNA?

The answer is Mutations! The 3 basic types of mutations are substitution, insertion, and deletion.


What are 3 types of mutation?

The three types of mutations are substitution (where one base is replaced with another), insertion (where an extra base is added), and deletion (where a base is removed). These mutations can alter the DNA sequence and potentially change the resulting protein.


What are 3 genetic mutations?

substitution and deletion, frameshift, translocation


Is SCID a frameshift mutation or a point mutation?

SCID can be caused by a variety of genetic mutations, including both frameshift and point mutations. Frameshift mutations involve the insertion or deletion of nucleotides that shifts the reading frame of a gene, while point mutations involve the substitution of a single nucleotide.


Changes in a DNA sequence caused by substitution of one nucleotide for another?

A substitution mutation occurs when one nucleotide in a DNA sequence is replaced with a different nucleotide. This can lead to a change in the corresponding amino acid in the protein produced from that gene, potentially altering the protein's structure and function. Substitution mutations can be silent (no change in the amino acid), missense (change in one amino acid), or nonsense (premature stop codon).


The substitution of one base for another during DNA replication is an example of what?

Mutations


What 3 mutations happen during cell division?

Insertion, Deletion, and Substitution


What role does substitution in DNA play in genetic mutations and inheritance?

Substitution in DNA can lead to genetic mutations, which are changes in the genetic code. These mutations can affect how traits are inherited from one generation to the next. Substitutions can alter the instructions for making proteins, potentially causing genetic disorders or variations in traits.


Which of the following statements about mutations and genetic disease are correct?

Mutations can result from spontaneous events or external mutagens. A change in DNA sequence may change the pattern of protein folding, resulting in genetic disease. Some genetic diseases may be caused by the substitution of only one incorrect amino acid in a protein. It is possible for the substitution of one base for another to have no effect on an organism.


What are examples of mutations and describe the consequences?

Examples of mutations include point mutations (substitution, insertion, deletion), chromosomal mutations (duplication, deletion, inversion, translocation), and silent mutations. These mutations can lead to various consequences such as changes in protein structure and function, genetic disorders, and cancer.


What are 4 type of mutation?

Four types of chromosomal mutations include substitution, insertion, deletion, and frame shift. These mutations can be either positive of negative to the organism.


What kind of mutation will result from the mistake made during DNA replication in the nucleotide sequence above?

The specific type of mutation resulting from a mistake during DNA replication will depend on the nature of the mistake and the type of nucleotide substitution that occurred. Some possible types of mutations include point mutations (such as a substitution, insertion, or deletion of a single nucleotide), frameshift mutations, or silent mutations.