Varaico: Literature-Extracted Genetic Variants

Gene:SMARCA4
Variant:p.W764R
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SMARCA4

NM_003072.5:p.W764R

Associated Papers

PRT3789 Is a First-in-Human SMARCA2-Selective Degrader That Induces Synthetic Lethality in SMARCA4-Mutated Cancers.

Hulse M et al.

Cancer Research, 2026

Functional characterization of SMARCA4 variants identified by targeted exome-sequencing of 131,668 cancer patients.

Fernando TM et al.

Nature Communications, 2020

33144586 (PubMed )
Supplement: 41467_2020_19402_MOESM6_ESM.xlsx › Sheet1

SMARCA4 deficiency-associated heterochromatin induces intrinsic DNA replication stress and susceptibility to ATR inhibition in lung adenocarcinoma.

Kurashima K et al.

Nar Cancer, 2020

34316685 (PubMed )
Supplement: narcancer_2_2_zcaa005_s8.pdf

Elucidation of the functional roles of the Q and I motifs in the human chromatin-remodeling enzyme BRG1.

Hoffmeister H et al.

The Journal of Biological Chemistry, 2019

Somatically mutated ABL1 is an actionable and essential NSCLC survival gene.

Testoni E et al.

Embo Molecular Medicine, 2016

26758680 (PubMed )
Supplement: EMMM-8-105-s006.xlsx › H2126_mutations_cBio

EZH2 inhibition sensitizes BRG1 and EGFR mutant lung tumours to TopoII inhibitors.

Fillmore CM et al.

Nature, 2015

25629630 (PubMed )
Supplement: NIHMS645459-supplement-1.pdf

Massive parallel DNA pyrosequencing analysis of the tumor suppressor BRG1/SMARCA4 in lung primary tumors.

Rodriguez-Nieto S et al.

Human Mutation, 2011

Frequent BRG1/SMARCA4-inactivating mutations in human lung cancer cell lines.

Medina PP et al.

Human Mutation, 2008

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."