KIT NP_000213.1:p.L862P

Preferred Label : KIT NP_000213.1:p.L862P;

NCIt synonyms : KIT p.Leu862Pro; Stem Cell Factor Receptor L862P; Mast/Stem Cell Growth Factor Receptor Kit L862P; NP_000213.1:p.L862P; KIT NP_000213.1:p.Leu862Pro; CD117 Antigen Leu862Pro; KIT L862P; KIT p.L862P; c-KIT Leu862Pro; c-KIT p.Leu862Pro; Proto-Oncogene c-Kit Leu862Pro; Tyrosine-Protein Kinase Kit Leu862Pro; CD117 Antigen L862P; Proto-Oncogene Tyrosine-Protein Kinase Kit Leu862Pro; c-KIT L862P; c-KIT p.L862P; Proto-Oncogene c-Kit L862P; Stem Cell Factor Receptor Leu862Pro; Tyrosine-Protein Kinase Kit L862P; Mast/Stem Cell Growth Factor Receptor Kit Leu862Pro; Proto-Oncogene Tyrosine-Protein Kinase Kit L862P; NP_000213.1:p.Leu862Pro; KIT Leu862Pro;

NCIt definition : A change in the amino acid residue at position 862 in the mast/stem cell growth factor receptor Kit protein where leucine has been replaced by proline.;

NCI Metathesaurus CUI : CL556215;

Details

Origin ID

C155724;

UMLS CUI

C4744353;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
gene_product_sequence_variation_encoded_by_gene_mutant
- KIT Exon 18 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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