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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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