SMARCA4 c.2842G>A ;(p.A948T)

Variant ID: 19-11132626-G-A

NM_003072.3(SMARCA4):c.2842G>A;(p.A948T)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A full-proteome, interaction-specific characterization of mutational hotspots across human cancers.

Genome Research
Chen, Siwei S; Liu, Yuan Y; Zhang, Yingying Y; Wierbowski, Shayne D SD; Lipkin, Steven M SM; Wei, Xiaomu X; Yu, Haiyuan H
Publication Date: 2022-01

Variant appearance in text: SMARCA4: A948T
PubMed Link: 34963661
Variant Present in the following documents:
  • supp_gr.275437.121_Supplementary_Table_1.xlsx, sheet 3
View BVdb publication page



Dramatic increase in gene mutational burden after transformation of follicular lymphoma into TdT+ B-lymphoblastic leukemia/lymphoma.

Cold Spring Harbor Molecular Case Studies
Belman, Jonathan P JP; Meng, Wenzhao W; Wang, Hong Yi HY; Li, Jie J; Strauser, Honore T HT; Rosenfeld, Aaron M AM; Zhang, Qian Q; Prak, Eline T Luning ETL; Wasik, Mariusz M
Publication Date: 2020-02

Variant appearance in text: SMARCA4: 2842G>A; A948T
PubMed Link: 31776129
Variant Present in the following documents:
  • Main text
  • MCS004614Bel.pdf
View BVdb publication page