C175689Level 7
Non-Synonymous TP53 Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the nucleotide sequence in the TP53 gene that encodes an amino acid substitution in the cellular tumor antigen p53 protein.
**Synonyms:** - Non-Synonymous LFS1 Gene Mutation - Non-Synonymous Li-Fraumeni Syndrome Gene Mutation - Non-Synonymous P53 Gene Mutation - Non-Synonymous TP53 Mutation - Non-Synonymous TRP53 Gene Mutation - Non-Synonymous Tumor Protein p53 Gene Mutation - Non-Synonymous p53 Mutation - Non-synonymous TP53 Gene Mutation - TP53 Gene Missense Mutation - TP53 Missense Mutation - p53 Missense Mutation
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