In genetics, a missense mutation is a point mutation in which a single nucleotide
change results ... MedTerms medical dictionary. MedicineNet. 2012-03-19.
Mar 2, 2009 ... A missense mutation may lead to the synthesis of a protein that is nonfunctional.
For instance in sicke-cell disease, the 20th nucleotide of the ...
a mutation in which a base change or substitution results in a codon that causes
insertion of a different amino acid into the growing polypeptide chain, giving rise
Missense definition at Dictionary.com, a free online dictionary with pronunciation,
... a codon altered through mutation so that it codes for a different amino acid.
What is the difference between a silent mutation, a missense mutation, a
nonsense mutation, and a frameshift mutation? Silent mutations - are caused by
a point ...
A missense mutation is a "readable" genetic message although its "sense" (its
meaning) is changed. This is in contrast to a nonsense mutation which has no ...
Missense mutation: A genetic change that results in the substitution of one amino
acid in protein for another. A missense mutation is responsible for sickle ...
With a missense mutation, the new nucleotide alters the codon so as to produce
an .... Just considering single-base substitutions, this means that each cell has 6
Sep 23, 2009 ... In a point mutation, a single base is substituted for another, changing the
meaning of a single codon, leaving the rest of the gene unchanged.
relating to or being a genetic mutation involving alteration of one or more codons
so that different amino acids are determined — compare antisense, nonsense.