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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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