POLE c.2971G>C ;(p.E991Q)

Variant ID: 12-133237644-C-G

NM_006231.2(POLE):c.2971G>C;(p.E991Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Finding driver mutations in cancer: Elucidating the role of background mutational processes.

Plos Computational Biology
Brown, Anna-Leigh AL; Li, Minghui M; Goncearenco, Alexander A; Panchenko, Anna R AR
Publication Date: 2019-04

Variant appearance in text: POLE: E991Q
PubMed Link: 31034466
Variant Present in the following documents:
  • pcbi.1006981.s010.xlsx, sheet 1
View BVdb publication page



Targeted next generation sequencing identified clinically actionable mutations in patients with esophageal sarcomatoid carcinoma.

Bmc Cancer
Lu, Hongyang H; Yang, Shifeng S; Zhu, Huineng H; Tong, Xiaoling X; Xie, Fajun F; Qin, Jing J; Han, Na N; Wu, Xue X; Fan, Yun Y; Shao, Yang W YW; Mao, Weimin W
Publication Date: 2018-03-05

Variant appearance in text: POLE: E991Q
PubMed Link: 29506494
Variant Present in the following documents:
  • Main text
  • 12885_2018_4159_MOESM2_ESM.xlsx, sheet 1
  • 12885_2018_Article_4159.pdf
View BVdb publication page