KIT c.677G>C ;(p.G226A)

Variant ID: 4-55565853-G-C

NM_000222.2(KIT):c.677G>C;(p.G226A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia.

Haematologica
Kaburagi, Taeko T; Yamato, Genki G; Shiba, Norio N; Yoshida, Kenichi K; Hara, Yusuke Y; Tabuchi, Ken K; Shiraishi, Yuichi Y; Ohki, Kentaro K; Sotomatsu, Manabu M; Arakawa, Hirokazu H; Matsuo, Hidemasa H; Shimada, Akira A; Taki, Tomohiko T; Kiyokawa, Nobutaka N; Tomizawa, Daisuke D; Horibe, Keizo K; Miyano, Satoru S; Taga, Takashi T; Adachi, Souichi S; Ogawa, Seishi S; Hayashi, Yasuhide Y
Publication Date: 2022-03-01

Variant appearance in text: KIT: G226A
PubMed Link: 33730843
Variant Present in the following documents:
  • 107583.pdf
View BVdb publication page



Comparing cell-free circulating tumor DNA mutational profiles of disease-free and nonresponders patients with oropharyngeal squamous cell carcinoma.

Laryngoscope Investigative Otolaryngology
Khandelwal, Alok R AR; Greer, Adam H AH; Hamiter, Mickie M; Fermin, Janmaris Marin JM; McMullen, Thomas T; Moore-Medlin, Tara T; Mills, Glenn G; Flores, Jose M JM; Yin, Hong H; Nathan, Cherie-Ann O CO
Publication Date: 2020-10

Variant appearance in text: KIT: Gly226Ala
PubMed Link: 33134534
Variant Present in the following documents:
  • Main text
View BVdb publication page