Bibliome.ai browser hg19
Search
About
Stats
FAQ
NOTCH1 c.2537A>C ;(p.Q846P)
Variant ID: 9-139405654-T-G
NM_017617.3(
NOTCH1
):c.2537A>C;(p.Q846P)
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:
A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.
Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01
Variant appearance in text: NOTCH1: Q846P
PubMed Link:
34963661
Variant Present in the following documents:
supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page
Clinical Features and Prognostic Significance of NOTCH1 Mutations in Diffuse Large B-Cell Lymphoma.
Frontiers In Oncology
Li, Zhongqi Z; Yu, Fang F; Ye, Wenle W; Mao, Liping L; Huang, Jiansong J; Shao, Yang Y; Yan, Junrong J; Yu, Wenjuan W; Jin, Jie J; Wang, Jinghan J
Publication Date: 2021
Variant appearance in text: NOTCH1: 2537A>C; Q846P
PubMed Link:
34956871
Variant Present in the following documents:
Main text
DataSheet_1.pdf
DataSheet_2.xlsx, sheet 1
fonc-11-746577.pdf
View BVdb publication page