KIT NM_000222.2:c.1669T A

Preferred Label : KIT NM_000222.2:c.1669T A;

NCIt synonyms : c-KIT c.1669T A; NM_000222.2:c.1669T A; KIT c.1669T A; CD117 c.1669T A; v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog c.1669T A; KIT Proto-Oncogene Tyrosine Protein Kinase c.1669T A;

NCIt related terms : KIT W557R (c.1669T A) mutation;

NCIt definition : A nucleotide substitution at position 1669 of the coding sequence of the KIT gene where thymine has been mutated to adenine.;

NCI Metathesaurus CUI : CL950789;

SNP ID : rs121913235;

Details

Origin ID

C158897;

UMLS CUI

C5204056;

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]
molecular_abnormality_involves_gene
- KIT Gene [NCIt concept]
- Receptor Tyrosine Kinase Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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