NOTCH1 c.4988G>A ;(p.R1663Q)

Variant ID: 9-139399155-C-T

NM_017617.3(NOTCH1):c.4988G>A;(p.R1663Q)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.

Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022

Variant appearance in text: NOTCH1: R1663Q
PubMed Link: 36072793
Variant Present in the following documents:
  • Table_3.xlsx, sheet 1
View BVdb publication page



In a multi-institutional cohort of myeloid sarcomas, NFE2 mutation prevalence is lower than previously reported.

Blood Advances
Anekpuritanang, Tauangtham T; Klairmont, Matthew M MM; Gradowski, Joel J; Hagiwara, Kohei K; Bailey, Nathanael G NG; Chandra, Pranil P; Liu, Yiwei Y; Mulder, Heather L HL; Easton, John J; Zhang, Jinghui J; Martin, Michael G MG; Owczarczyk, Anna B AB; Dunlap, Jennifer B JB; Fan, Guang G; Press, Richard D RD; Raess, Philipp W PW
Publication Date: 2021-12-14

Variant appearance in text: NOTCH1: R1663Q
PubMed Link: 34559205
Variant Present in the following documents:
  • advancesADV2021004983-suppl1.pdf
View BVdb publication page