FOXL2 NM_023067.4:c.402C>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 402 of the coding sequence of the FOXL2 gene where cytosine has been mutated to guanine.

**Synonyms:** - FOXL2 c.402C>G - Forkhead Box L2 c.402C>G - NM_023067.4:c.402C>G - PFRK c.402C>G - PINTO c.402C>G - POF3 c.402C>G