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POLE c.1736G>T ;(p.R579L)
Variant ID: 12-133248859-C-A
NM_006231.2(
POLE
):c.1736G>T;(p.R579L)
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:
HRAS Q61L Mutation as a Possible Target for Non-Small Cell Lung Cancer: Case Series and Review of Literature.
Current Oncology (Toronto, Ont.)
Mathiot, Laurent L; Herbreteau, Guillaume G; Robin, Siméon S; Fenat, Charlotte C; Bennouna, Jaafar J; Blanquart, Christophe C; Denis, Marc M; Pons-Tostivint, Elvire E
Publication Date: 2022-05-20
Variant appearance in text: POLE: Arg579Leu
PubMed Link:
35621690
Variant Present in the following documents:
curroncol-29-00300.pdf
View BVdb publication page
Clinical and genomic features of Chinese lung cancer patients with germline mutations.
Nature Communications
Peng, Wenying W; Li, Bin B; Li, Jin J; Chang, Lianpeng L; Bai, Jing J; Yi, Yuting Y; Chen, Rongrong R; Zhang, Yanyan Y; Chen, Chen C; Pu, Xingxiang X; Jiang, Meilin M; Li, Jia J; Zhong, Rui R; Xu, Fang F; Chen, Bolin B; Xu, Li L; Wang, Ning N; Huan, Jiaojiao J; Dai, Pingping P; Guan, Yanfang Y; Yang, Ling L; Xia, Xuefeng X; Yi, Xin X; Wang, Jiayin J; Yu, Fenglei F; Wu, Lin L
Publication Date: 2022-03-10
Variant appearance in text: POLE: 1736G>T; R579L
PubMed Link:
35273153
Variant Present in the following documents:
41467_2022_28840_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page