Nonsense mutation

From The School of Biomedical Sciences Wiki
Revision as of 20:18, 10 December 2018 by Nnjm2 (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

Nonsense mutation is when there is a nucleotide substitution causing a different amino acid to be coded for, which creates a stop codon . This causes the protein that is being encoded for to be truncated due to the premature termination of translation[1].

References

  1. ↑ Hartl, D. and Jones, E. (2009) Genetics: Genes and Genomes, U.S.A: Jones and Bartlett, page 515
Retrieved from "https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Nonsense_mutation&oldid=23689"