TP53 NM_000546.5:c.742C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 742 of the coding sequence of the TP53 gene where cytosine has been mutated to thymine.

**Synonyms:** - LFS1 c.742C>T - Li-Fraumeni Syndrome c.742C>T - NM_000546.5:c.742C>T - P53 c.742C>T - TP53 c.742C>T - Tumor Protein p53 c.742C>T