C223938Level 7
PDGFRA NM_006206.6:c.2525_2529delinsTCATG
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A complex nucleotide substitution with a deletion of five nucleotides from the coding sequence of the PDGFRA gene from position 2525 through 2529 and with an insertion of five nucleotides, thymine-cytosine-adenine-thymine-guanine.
**Synonyms:** - CD140A c.2525_2529delinsTCATG - NM_006206.6:c.2525_2529delinsTCATG - NM_006206.6:c.[2525A>T;2529C>G] - PDGFR-2 c.2525_2529delinsTCATG - PDGFR2 c.2525_2529delinsTCATG - PDGFRA c.2525_2529ACATC>TCATG - PDGFRA c.2525_2529delACATCinsTCATG - PDGFRA c.2525_2529delinsTCATG - Platelet-Derived Growth Factor Receptor, Alpha Polypeptide c.2525_2529delinsTCATG - RHEPDGFRA c.2525_2529delinsTCATG
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Cross-system equivalences0
No cross-system equivalences mapped for this node.