NOTCH1 c.3632G>A ;(p.R1211Q)

Variant ID: 9-139401768-C-T

NM_017617.3(NOTCH1):c.3632G>A;(p.R1211Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutation allele frequency threshold does not affect prognostic analysis using next-generation sequencing in oral squamous cell carcinoma.

Bmc Cancer
Ma, Jie J; Fu, Yong Y; Tu, Yao-Yao YY; Liu, Ying Y; Tan, Yi-Ran YR; Ju, Wu-Tong WT; Pickering, Curtis R CR; Myers, Jeffrey N JN; Zhang, Zhi-Yuan ZY; Zhong, Lai-Ping LP
Publication Date: 2018-07-24

Variant appearance in text: NOTCH1: Arg1211Gln
PubMed Link: 30041611
Variant Present in the following documents:
  • Main text
  • 12885_2018_Article_4481.pdf
View BVdb publication page