BRAF NM_004333.4:c.1796_1797insTAC

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A genetic variation where the trinucleotide, thymine-adenine-cytosine, has been inserted between the nucleotides at positions 1796 and 1797 of the coding sequence of the BRAF gene.

**Synonyms:** - B-RAF c.1796_1797insTAC - BRAF c.1796_1797insTAC - BRAF c.1798insTAC - NM_004333.4:c.1796_1797insTAC - NM_004333.6:c.1794_1796dup - v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1796_1797insTAC