C136635Level 6
Non-synonymous KIT Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in the KIT gene that encodes an amino acid substitution in the mast/stem cell growth factor receptor Kit protein.
**Synonyms:** - C-KIT Missense Mutation - KIT Missense Mutation - Non-synonymous CD117 Gene Mutation - Non-synonymous KIT Proto-Oncogene Tyrosine Protein Kinase Gene Mutation - Non-synonymous V-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Mutation - Non-synonymous c-KIT Gene Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C136635Hierarchy Explorer
Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.