KIT NM_000222.2:c.1669T>A

**Semantic type:** Cell or Molecular Dysfunction

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

**Synonyms:** - CD117 c.1669T>A - KIT Proto-Oncogene Tyrosine Protein Kinase c.1669T>A - KIT W557R (c.1669T>A) mutation - KIT c.1669T>A - NM_000222.2:c.1669T>A - c-KIT c.1669T>A - v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog c.1669T>A