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What is the definition of chromosome mutation?

Updated: 8/17/2019
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A chromosome is an organized structure of DNA and protein that is found in cells.In Biology, mutations are changes to the nucleotide sequence of the genetic material of an organism.

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Q: What is the definition of chromosome mutation?
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Related questions

What is the term for any permanent change in a gene of chromosome?

The permanent change in a gene or a chromosome is called Mutation.


What is an mutation?

An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.


Whats a change in gene or chromosome?

A change in a gene or chromosome is called a: Mutation


What is a change or error in the structure of a gene or chromosome?

Chromosomal mutation


Mutation is any change in a gene or chromosome?

mutations


What are four of chromosomal mutation?

Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).


Which types of mutation can be add genes to a chromosome?

A deletion mutation can take genes away from a chromosome.


Which is worse chromosome mutation or point mutation?

choromosome mutaion


What are four types of chromosomal mutations?

Four types of chromosomal mutations are Down syndrome (which is a mutation in which there are three copies of chromosome 21), Kinefelter Syndrome (which is a mutation in which a male has an extra X-chromosome), Turner Syndrome (which is a mutation in which a female is missing an X-chromosome), and Patau Syndrome (which is a mutation in which there are three copies of chromosome 13).


What is chromosome change called?

Mutation


Any permanent change in gene or chromosome of a cell?

Mutation


What is the resulting mutation when a a piece of chromosome attaches itself to a nonhomologous chromosome?

Translocations