Varaico: Literature-Extracted Genetic Variants

Gene:SMARCA4
Variant:p.L1163P
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SMARCA4

NM_003072.5:p.L1163P

Associated Papers

A comprehensive benchmark for multiple highly efficient base editors with broad targeting scope.

Wang X et al.

Biorxiv : the Preprint Server for Biology, 2025

39763781 (PubMed )
Supplement: media-3.xlsx › ABE_screen_library

PHF6 cooperates with SWI/SNF complexes to facilitate transcriptional progression.

Mittal P et al.

Nature Communications, 2024

39181868 (PubMed )
Supplement: 41467_2024_51566_MOESM2_ESM.pdf

SinoDuplex: An Improved Duplex Sequencing Approach to Detect Low-frequency Variants in Plasma cfDNA Samples.

Ren Y et al.

Genomics, Proteomics & Bioinformatics, 2020

32428603 (PubMed )
Supplement: mmc6.xlsx › HD701

Development of a targeted sequencing approach to identify prognostic, predictive and diagnostic markers in paediatric solid tumours.

Izquierdo E et al.

Oncotarget, 2017

29340109 (PubMed )
Supplement: oncotarget-08-112036-s003.xlsx › A.Total_background_variants

A synthetic lethality-based strategy to treat cancers harboring a genetic deficiency in the chromatin remodeling factor BRG1.

Oike T et al.

Cancer Research, 2013

The chromatin remodelling factor BRG1 is a novel binding partner of the tumor suppressor p16INK4a.

Becker TM et al.

Molecular Cancer, 2009

Involvement of the chromatin-remodeling factor BRG1/SMARCA4 in human cancer.

Medina PP et al.

Epigenetics, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."