Point mutation
From Biocrawler, the free encyclopedia.
A point mutation is a type of mutation that causes the replacement of a single base pair with another pair. There are several types of point mutations:
- nonsense mutations: codes for a stop, which can truncate the protein
- missense mutations: codes for a different amino acid
- silent mutations: codes for the same amino acid, so has no effect
For example, sickle-cell anemia is caused by a single point mutation in the beta hemoglobin gene that converts a GAG codon into GTG, which encodes the amino acid valine rather than glutamic acid.
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