Difference between revisions of "Point mutation"

From Conservapedia
Jump to navigation Jump to search
(Redirecting to Mutation)
 
(3 intermediate revisions by 3 users not shown)
Line 1: Line 1:
 +
#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".
 
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.
 
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.
  
A point mutation cannot add new information to the genome. <ref>AIG article [http://www.answersingenesis.org/articles/2008/02/01/feedback-new-information]</ref>
+
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}}
 
{{reflist}}

Latest revision as of 15:31, February 4, 2009

Redirect to:

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]

  1. ↑ Purdom, Georgia, Feedback: Evidence of New Genetic Information?, 1st February, 2009 (Answers in Genesis)