C98354Level 7
BRAF NM_004333.4:c.1798_1799delinsAG
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A complex substitution where the nucleotide sequence at positions 1798 and 1799 of the coding sequence of the BRAF gene has changed from guanine-thymine to adenine-guanine.
**Synonyms:** - B-RAF1 c.1798_1799GT>AG - BRAF NM_004333.4:c.1798_1799delGTinsAG - BRAF NM_004333.4:c.1798_1799delGTinsAG - BRAF V600R (c.1798_1799GT>AG) mutation - BRAF c.1798_1799GT>AG - BRAF c.1798_1799delGTinsAG - NM_004333.4:c.1798_1799GT>AG - NM_004333.4:c.1798_1799delGTinsAG - NM_004333.4:c.1798_1799delinsAG - NM_004333.6:c.1798_1799delinsAG - v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1798_1799GT>AG
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Cross-system equivalences0
No cross-system equivalences mapped for this node.