C20629Level 6
Silent Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation occurring within the protein-coding region of a gene, and which codes for the same amino acid as expected.
**Synonyms:** - Exon Synonymous Mutation - Exonic Synonymous Mutation - Mutation, Silent - Synonymous - Synonymous Mutation - Synonymous Variant - Synonymous Variant
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