KIT c.189T>C ;(p.F63=)

Variant ID: 4-55561799-T-C

NM_000222.2(KIT):c.189T>C;(p.F63=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A case of acute myeloid leukemia with promyelocytic features characterized by expression of a novel RARG-CPSF6 fusion.

Blood Advances
Miller, Christopher A CA; Tricarico, Christopher C; Skidmore, Zachary L ZL; Uy, Geoffrey L GL; Lee, Yi-Shan YS; Hassan, Anjum A; O'Laughlin, Michelle D MD; Schmidt, Heather H; Tian, Ling L; Duncavage, Eric J EJ; Griffith, Malachi M; Griffith, Obi L OL; Welch, John S JS; Wartman, Lukas D LD
Publication Date: 2018-06-12

Variant appearance in text: CD117: F63F
PubMed Link: 29891591
Variant Present in the following documents:
  • Main text
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