BRAF NM_004333.4:c.1799T>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1799 of the coding sequence of the BRAF gene where thymine has been mutated to adenine.

**Synonyms:** - B-RAF1 c.1799T>A - BRAF V600E (c.1799T>A) mutation - BRAF c.1799T>A - NM_004333.4:c.1799T>A - v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1799T>A