KIT c.1085A>T ;(p.Y362F)

Variant ID: 4-55573423-A-T

NM_000222.2(KIT):c.1085A>T;(p.Y362F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The reliable assurance of detecting somatic mutations in cancer-related genes by next-generation sequencing: the results of external quality assessment in China.

Oncotarget
Zhang, Rui R; Ding, Jiansheng J; Han, Yanxi Y; Yi, Lang L; Xie, Jiehong J; Yang, Xin X; Fan, Gaowei G; Wang, Guojing G; Hao, Mingju M; Zhang, Dong D; Zhang, Kuo K; Lin, Guigao G; Li, Jinming J
Publication Date: 2016-09-06

Variant appearance in text: KIT: 1085A>T; Tyr362Phe
PubMed Link: 27542269
Variant Present in the following documents:
  • Main text
  • oncotarget-07-58500.pdf
View BVdb publication page



Targeted next generation sequencing identifies clinically actionable mutations in patients with melanoma.

Pigment Cell & Melanoma Research
Jeck, William R WR; Parker, Joel J; Carson, Craig C CC; Shields, Janiel M JM; Sambade, Maria J MJ; Peters, Eldon C EC; Burd, Christin E CE; Thomas, Nancy E NE; Chiang, Derek Y DY; Liu, Wenjin W; Eberhard, David A DA; Ollila, David D; Grilley-Olson, Juneko J; Moschos, Stergios S; Neil Hayes, D D; Sharpless, Norman E NE
Publication Date: 2014-07

Variant appearance in text: KIT: Y362F
PubMed Link: 24628946
Variant Present in the following documents:
  • Main text
View BVdb publication page