BRAF NM_004333.4:c.1798_1799delinsAG

Preferred Label : BRAF NM_004333.4:c.1798_1799delinsAG;

NCIt synonyms : BRAF c.1798_1799delGTinsAG; B-RAF1 c.1798_1799GT AG; NM_004333.4:c.1798_1799GT AG; NM_004333.4:c.1798_1799delGTinsAG; BRAF c.1798_1799GT AG; v-raf Murine Sarcoma Viral Oncogene Homolog B1 c.1798_1799GT AG; NM_004333.6:c.1798_1799delinsAG; NM_004333.4:c.1798_1799delinsAG;

NCIt related terms : BRAF V600R (c.1798_1799GT AG) mutation; BRAF NM_004333.4:c.1798_1799delGTinsAG;

NCIt 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.;

Détails

Origin ID

C98354;

UMLS CUI

C3274002;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- CPTAC Baseline Medical Forms Terminology [NCIt concept]
- CPTAC Melanoma Baseline Form [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_mutant_encodes_gene_product_sequence_variation
- BRAF NP_004324.2:p.V600R [NCIt concept]
- BRAF Protein Variant [NCIt concept]
molecular_abnormality_involves_gene
- BRAF Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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