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NOTCH1 c.5378G>A ;(p.G1793D)
Variant ID: 9-139396730-C-T
NM_017617.3(
NOTCH1
):c.5378G>A;(p.G1793D)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Integrating real-time in vivo tumour genomes for longitudinal analysis and management of glioma recurrence.
Clinical And Translational Medicine
Sheng, Zhiyuan Z; Yu, Jinliang J; Deng, Kaiyuan K; Bu, Yage Y; Wu, Shuang S; Xu, Sensen S; Gao, Yushuai Y; Zhang, Qianqian Q; Yan, Zhaoyue Z; Bu, Chaojie C; Chen, Zhongcan Z; Gu, Jianjun J; Jia, Yan Y; Gao, Xinya X; Zemmar, Ajmal A; Sumardi, Fitri F; Hernesniemi, Juha J; Kong, Lingfei L; Liu, Gang G; Li, Ming M; Wang, Meiyun M; Li, Tianxiao T; Bu, Xingyao X
Publication Date: 2021-11
Variant appearance in text: NOTCH1: 5378G>A; Gly1793Asp
PubMed Link:
34841677
Variant Present in the following documents:
CTM2-11-e567-s004.xlsx, sheet 5
View BVdb publication page