BRAF NM_004333.4:c.1797_1798insACA

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A genetic variation where the trinucleotide, adenine-cytosine-adenine, has been inserted between the nucleotides at positions 1797 and 1798 of the coding sequence of the BRAF gene.

**Synonyms:** - B-RAF1 c.1797_1798insACA - BRAF c.1795_1797dup - BRAF c.1797_1798insACA - NM_004333.4:c.1795_1797dup - NM_004333.4:c.1795_1797dupACA - NM_004333.4:c.1797_1798insACA - v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1797_1798insACA