silent mutation
Sign in to savepoint mutation where a codon is substituted with another codon that encodes the same amino acid
Research
5,501 papers- The Silent Mutation.JAMA · 2021
- Novel homozygous silent mutation of ITGB3 gene caused Glanzmann thrombasthenia.Frontiers in pediatrics · 2022
- Silent mutation in long QT syndrome: pathogenicity prediction by computer simulation.Heart rhythm · 2012
- Synonymous mutations promote tumorigenesis by disrupting m(6)A-dependent mRNA metabolism.Cell · 2025
- Silent mutations make noise.Nature reviews. Cancer · 2022
via PubMed
Wikidata facts
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- www.sequenceontology.org/browser/current_svn/term/SO:0001017
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- Silent mutation
Sources (3)
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Connections
standard genetic code
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messenger RNA
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transfer RNA
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Synonymous substitution
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deoxyribonucleic acid
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International Standard Book Number
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poliomyelitis
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amino acid
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natural selection
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mitochondrion
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digital object identifier
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ribosome
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mutation
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cloning
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cytoplasm
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peptide
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Q180686
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transcription
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tryptophan
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L-leucine
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