C98624Level 5
EGFR NP_005219.2:p.V769_D770insDNV
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** An insertion of the amino acid sequence aspartic acid-asparagine-valine between the valine at position 769 and the aspartic acid at position 770 of the epidermal growth factor receptor protein.
**Synonyms:** - EGFR NP_005219.2:p.V769_N771dup - EGFR NP_005219.2:p.Val769_Asp770insAspAsnVal - EGFR V769_D770insDNV - EGFR V769_N771 Duplication Mutation - EGFR p.V769_D770insDNV - Epidermal Growth Factor Receptor V769_D770insDNV - NP_005219.2:p.V769_N771dup - NP_005219.2:p.Val769_Asn771dup - NP_005219.2:p.Val769_Asp770insAspAsnVal - Proto-Oncogene c-ErbB-1 V769_D770insDNV - Receptor Tyrosine-Protein Kinase erbB-1 V769_D770insDNV
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Cross-system equivalences0
No cross-system equivalences mapped for this node.