C44521Level 6
t(3;14)(p14.1;q32)
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A chromosomal translocation involving breakpoints within the p14.1 band on the short arm of chromosome 3 and the q32 band on the long arm of chromosome 14. This rearrangement is associated with aberrant expression of the FOXP1 gene and extranodal mucosa-associated lymphoid tissue (MALT) lymphoma.
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