C175695Level 7
Non-Synonymous PTEN Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the nucleotide sequence in the PTEN gene that encodes an amino acid substitution in the phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN protein.
**Synonyms:** - Non-Synonymous MMAC1 Gene Mutation - Non-Synonymous Mutated in Multiple Advanced Cancers 1 Gene Mutation - Non-Synonymous PTEN Mutation - Non-Synonymous PTEN1 Gene Mutation - Non-Synonymous Phosphatase and Tensin Homolog Gene Mutation - Non-Synonymous TEP1 Gene Mutation - Non-synonymous PTEN Gene Mutation - PTEN Gene Missense Mutation - PTEN Missense Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C175695Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.