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NOTCH1 c.5021C>T ;(p.S1674F)
Variant ID: 9-139397780-G-A
NM_017617.3(
NOTCH1
):c.5021C>T;(p.S1674F)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Somatic mutation distribution across tumour cohorts provides a signal for positive selection in cancer.
Nature Communications
Boström, Martin M; Larsson, Erik E
Publication Date: 2022-11-17
Variant appearance in text: NOTCH1: S1674F
PubMed Link:
36396655
Variant Present in the following documents:
41467_2022_34746_MOESM10_ESM.xlsx, sheet 1
View BVdb publication page
Diversity spectrum analysis identifies mutation-specific effects of cancer driver genes.
Communications Biology
Dong, Xiaobao X; Huang, Dandan D; Yi, Xianfu X; Zhang, Shijie S; Wang, Zhao Z; Yan, Bin B; Chung Sham, Pak P; Chen, Kexin K; Jun Li, Mulin M
Publication Date: 2020-01-07
Variant appearance in text: NOTCH1: 5021C>T; S1674F
PubMed Link:
31925297
Variant Present in the following documents:
42003_2019_736_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers.
Jama Network Open
Khater, Fida F; Vairy, Stephanie S; Langlois, Sylvie S; Dumoucel, Sophie S; Sontag, Thomas T; St-Onge, Pascal P; Bittencourt, Henrique H; Dal Soglio, Dorothée D; Champagne, Josette J; Duval, Michel M; Leclerc, Jean-Marie JM; Laverdiere, Caroline C; Tran, Thai Hoa TH; Patey, Natalie N; Ellezam, Benjamin B; Perreault, Sébastien S; Piché, Nelson N; Samson, Yvan Y; Teira, Pierre P; Jabado, Nada N; Michon, Bruno B; Brossard, Josée J; Marzouki, Monia M; Cellot, Sonia S; Sinnett, Daniel D
Publication Date: 2019-04-05
Variant appearance in text: NOTCH1: S1674F
PubMed Link:
31026031
Variant Present in the following documents:
Main text
View BVdb publication page