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NOTCH1 c.4776C>G ;(p.F1592L)
Variant ID: 9-139399367-G-C
NM_017617.3(
NOTCH1
):c.4776C>G;(p.F1592L)
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:
Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia.
Scientific Reports
Chang, Ya-Hsuan YH; Yu, Chih-Hsiang CH; Jou, Shiann-Tarng ST; Lin, Chien-Yu CY; Lin, Kai-Hsin KH; Lu, Meng-Yao MY; Wu, Kang-Hsi KH; Chang, Hsiu-Hao HH; Lin, Dong-Tsamn DT; Lin, Shu-Wha SW; Chen, Hsuan-Yu HY; Yang, Yung-Li YL
Publication Date: 2021-01-12
Variant appearance in text: NOTCH1: F1592L
PubMed Link:
33436855
Variant Present in the following documents:
41598_2020_80613_MOESM1_ESM.pdf
View BVdb publication page
Co-existence of PHF6 and NOTCH1 mutations in adult T-cell acute lymphoblastic leukemia.
Oncology Letters
Li, Min M; Xiao, Lichan L; Xu, Jingyan J; Zhang, Run R; Guo, Jingjing J; Olson, Justin J; Wu, Yujie Y; Li, Jianyong J; Song, Chunhua C; Ge, Zheng Z
Publication Date: 2016-07
Variant appearance in text: NOTCH1: F1592L
PubMed Link:
27347093
Variant Present in the following documents:
Main text
ol-12-01-0016.pdf
View BVdb publication page