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.




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