Difference between revisions of "Point mutation"
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| − | A ''' | + | #REDIRECT [[Mutation]] |
| + | A '''point mutation''' is the most limited type of [[mutation]], whereby a single base [[nucleotide]] is replaced with another nucleotide. Sometimes the expression "point mutation" can also include the addition or subtraction of a single base pair, which is also referred to as an "indel". | ||
| − | + | The sickle-cell disease is caused by a single point mutation in one allele of the beta [[hemoglobin]] gene, whereby a CCT codon is converted into TCT. The TCT then mistakenly encodes the [[amino acid]] serine instead of proline. | |
| − | [[ | + | Point mutations do not add new information to the genome. <ref>Purdom, Georgia, [http://www.answersingenesis.org/articles/2008/02/01/feedback-new-information Feedback: Evidence of New Genetic Information?], 1st February, 2009 (Answers in Genesis)</ref> |
| − | [[ | + | |
| − | + | {{reflist}} | |
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| + | [[Category:genetics]] | ||
| + | [[Category:diseases]] | ||
Latest revision as of 15:31, February 4, 2009
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A point mutation is the most limited type of mutation, whereby a single base nucleotide is replaced with another nucleotide. Sometimes the expression "point mutation" can also include the addition or subtraction of a single base pair, which is also referred to as an "indel".
The sickle-cell disease is caused by a single point mutation in one allele of the beta hemoglobin gene, whereby a CCT codon is converted into TCT. The TCT then mistakenly encodes the amino acid serine instead of proline.
Point mutations do not add new information to the genome. [1]
- â Purdom, Georgia, Feedback: Evidence of New Genetic Information?, 1st February, 2009 (Answers in Genesis)