C175694Level 7
Non-Synonymous RB1 Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the nucleotide sequence in the RB1 gene that encodes an amino acid substitution in the retinoblastoma-associated protein.
**Synonyms:** - Non-Synonymous RB Gene Mutation - Non-Synonymous RB Mutation - Non-Synonymous RB1 Mutation - Non-Synonymous Retinoblastoma 1 Gene Mutation - Non-Synonymous Retinoblastoma Gene Mutation - Non-synonymous RB1 Gene Mutation - RB Missense Mutation - RB1 Gene Missense Mutation - RB1 Missense Mutation
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