Missense mutation
Missense mutation
Genetic point mutation that results in an amino acid change in a protein.
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Readers' pathsAug 2026 – Oct 2026
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Point mutation
Replacement, insertion, or deletion of a single DNA or RNA nucleotide.
26%
Rett syndrome
Genetic brain disorder.
16%
Genetic code
Rules by which information encoded within genetic material is translated into proteins.
8.7%
Silent mutation
DNA mutation with no observable effect on an organism's phenotype.
5.3%
Nucleotide
Biological molecules constituting nucleic acids.
3.2%
Readers come from
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Kuru (disease)
Rare neurodegenerative disease caused by prions.
38%
Fatal insomnia
Prion disease of the human brain.
15%
Genetic code
Rules by which information encoded within genetic material is translated into proteins.
9.3%
Variants of SARS-CoV-2
6.9%
Crouzon syndrome
Genetic disorder of the skull and face.
6.5%
Sea otter
Species of marine mammal.
2.5%
Japanese Bobtail
Breed of cat.
2%
Li–Fraumeni syndrome
Autosomal dominant cancer syndrome.
1.8%
Mutation
Alteration in the nucleotide sequence of a genome.
1.7%