PTEN NM_000314.7:c.389G>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 389 of the coding sequence of the PTEN gene where guanine has been mutated to thymine.

**Synonyms:** - MMAC1 c.389G>T - Mutated in Multiple Advanced Cancers 1 c.389G>T - NM_000314.7:c.389G>T - PTEN c.389G>T - PTEN1 c.389G>T - Phosphatase and Tensin Homolog c.389G>T - TEP1 c.389G>T