Silent mutation: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
A silent mutation is a mutation in a [[Nucleotide|nucleotide]] sequence, which does not change the sequence of [[Amino acid|amino acids]]. Even regions outside the coding sequence could be affected by a silent mutation. In non-coding regions in [[DNA|DNA]], the [[Nucleotide|nucleotide sequence]] does not have [[Base|bases]] needed for the [[Protein|protein]] required<ref>Daniel L. Hartl and Elizabeth W. Jones (2009) Genetics: Genes and Genomes, 7th Edition, London, Jones and Bartlett Publishers, pg 513</ref>. | |||
Silent mutations do not affect the phenotype as there are no change in amino acid sequence<ref>http://ghr.nlm.nih.gov/glossary=silentmutation November 24, 2014.</ref>. | Silent mutations do not affect the phenotype as there are no change in amino acid sequence<ref>http://ghr.nlm.nih.gov/glossary=silentmutation November 24, 2014.</ref>.<br> | ||
<br> | |||
=== References: === | === References: === | ||
Revision as of 06:58, 26 November 2014
A silent mutation is a mutation in a nucleotide sequence, which does not change the sequence of amino acids. Even regions outside the coding sequence could be affected by a silent mutation. In non-coding regions in DNA, the nucleotide sequence does not have bases needed for the protein required[1].
Silent mutations do not affect the phenotype as there are no change in amino acid sequence[2].
References:
- ↑ Daniel L. Hartl and Elizabeth W. Jones (2009) Genetics: Genes and Genomes, 7th Edition, London, Jones and Bartlett Publishers, pg 513
- ↑ http://ghr.nlm.nih.gov/glossary=silentmutation November 24, 2014.