KIT c.2465_2466delinsGG ;(p.N822R)

Variant ID: 4-55599339-AT-GG

NM_000222.2(KIT):c.2465_2466delinsGG;(p.N822R)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: KIT: N822R
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



SKP2 high expression, KIT exon 11 deletions, and gastrointestinal bleeding as predictors of poor prognosis in primary gastrointestinal stromal tumors.

Plos One
Lv, Ang A; Li, Zhongwu Z; Tian, Xiuyun X; Guan, Xiaoya X; Zhao, Min M; Dong, Bin B; Hao, Chunyi C
Publication Date: 2013

Variant appearance in text: KIT: N822R
PubMed Link: 23690967
Variant Present in the following documents:
  • Main text
  • pone.0062951.pdf
View BVdb publication page