t(3;12)(q27-28;q13-15)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A chromosomal translocation involving breakpoints within the q27-q28 region on the long arm of chromosome 3 and the q13-q15 region on the long arm of chromosome 12. This rearrangement may be associated with HMGA2-LPP fusion gene expression and lipoma.

**Synonyms:** - t(3;12)(q27-q28;q13-q15)