KIT NP_000213.1:p.G648D

Preferred Label : KIT NP_000213.1:p.G648D;

NCIt synonyms : Tyrosine-Protein Kinase Kit Gly648Asp; Proto-Oncogene Tyrosine-Protein Kinase Kit Gly648Asp; CD117 Antigen G648D; c-KIT G648D; Stem Cell Factor Receptor Gly648Asp; c-KIT p.G648D; Proto-Oncogene c-Kit G648D; Mast/Stem Cell Growth Factor Receptor Kit Gly648Asp; NP_000213.1:p.Gly648Asp; Tyrosine-Protein Kinase Kit G648D; Proto-Oncogene Tyrosine-Protein Kinase Kit G648D; KIT Gly648Asp; KIT p.Gly648Asp; Stem Cell Factor Receptor G648D; KIT NP_000213.1:p.Gly648Asp; Mast/Stem Cell Growth Factor Receptor Kit G648D; CD117 Antigen Gly648Asp; NP_000213.1:p.G648D; c-KIT Gly648Asp; c-KIT p.Gly648Asp; KIT G648D; KIT p.G648D; Proto-Oncogene c-Kit Gly648Asp;

NCIt definition : A change in the amino acid residue at position 648 in the mast/stem cell growth factor receptor Kit protein where glycine has been replaced by aspartic acid.;

NCI Metathesaurus CUI : CL556289;

Details

Origin ID

C155684;

UMLS CUI

C4745303;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_product_sequence_variation_encoded_by_gene_mutant
- KIT Exon 13 Mutation [NCIt concept]
- KIT Gene Mutation [NCIt concept]
gene_product_variant_of_gene_product
- Mast/Stem Cell Growth Factor Receptor Kit [NCIt concept]
molecular_abnormality_involves_gene
- KIT Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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