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NOTCH1 c.892G>T ;(p.E298*)
Variant ID: 9-139413250-C-A
NM_017617.3(
NOTCH1
):c.892G>T;(p.E298*)
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:
Identification of predictors of drug sensitivity using patient-derived models of esophageal squamous cell carcinoma.
Nature Communications
Su, Dan D; Zhang, Dadong D; Jin, Jiaoyue J; Ying, Lisha L; Han, Miao M; Chen, Kaiyan K; Li, Bin B; Wu, Junzhou J; Xie, Zhenghua Z; Zhang, Fanrong F; Lin, Yihui Y; Cheng, Guoping G; Li, Jing-Yu JY; Huang, Minran M; Wang, Jinchao J; Wang, Kailai K; Zhang, Jianjun J; Li, Fugen F; Xiong, Lei L; Futreal, Andrew A; Mao, Weimin W
Publication Date: 2019-11-07
Variant appearance in text: NOTCH1: 892G>T; Glu298*
PubMed Link:
31700061
Variant Present in the following documents:
41467_2019_12846_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page
Small Cell Lung Cancer Exhibits Frequent Inactivating Mutations in the Histone Methyltransferase KMT2D/MLL2: CALGB 151111 (Alliance).
Journal Of Thoracic Oncology : Official Publication Of The International Association For The Study Of Lung Cancer
Augert, Arnaud A; Zhang, Qing Q; Bates, Breanna B; Cui, Min M; Wang, Xiaofei X; Wildey, Gary G; Dowlati, Afshin A; MacPherson, David D
Publication Date: 2017-04
Variant appearance in text: NOTCH1: E298X
PubMed Link:
28007623
Variant Present in the following documents:
Main text
View BVdb publication page