EGR1 c.1091G>C ;(p.G364A)

Variant ID: 5-137803229-G-C

NM_001964.2(EGR1):c.1091G>C;(p.G364A)

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: 225: G364A
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 9
View BVdb publication page



Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma.

Neuro-Oncology Advances
Jones, Lindsey E LE; Hilz, Stephanie S; Grimmer, Matthew R MR; Mazor, Tali T; Najac, ChloƩ C; Mukherjee, Joydeep J; McKinney, Andrew A; Chow, Tracy T; Pieper, Russell O RO; Ronen, Sabrina M SM; Chang, Susan M SM; Phillips, Joanna J JJ; Costello, Joseph F JF
Publication Date: 2020

Variant appearance in text: 225: G364A
PubMed Link: 32904945
Variant Present in the following documents:
  • vdaa088_suppl_supplementary_tables.xlsx, sheet 2
View BVdb publication page



Characterization of genome-wide variations induced by gamma-ray radiation in barley using RNA-Seq.

Bmc Genomics
Tan, Cong C; Zhang, Xiao-Qi XQ; Wang, Yin Y; Wu, Dianxin D; Bellgard, Matthew I MI; Xu, Yanhao Y; Shu, Xiaoli X; Zhou, Gaofeng G; Li, Chengdao C
Publication Date: 2019-10-29

Variant appearance in text: 225: 1091G>C
PubMed Link: 31664908
Variant Present in the following documents:
  • 12864_2019_6182_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Comparative analysis of primary versus relapse/refractory DLBCL identifies shifts in mutation spectrum.

Oncotarget
Greenawalt, Danielle M DM; Liang, Winnie S WS; Saif, Sakina S; Johnson, Justin J; Todorov, Petar P; Dulak, Austin A; Enriquez, Daniel D; Halperin, Rebecca R; Ahmed, Ambar A; Saveliev, Vladislav V; Carpten, John J; Craig, David D; Barrett, J Carl JC; Dougherty, Brian B; Zinda, Michael M; Fawell, Stephen S; Dry, Jonathan R JR; Byth, Kate K
Publication Date: 2017-11-21

Variant appearance in text: 225: 1091G>C
PubMed Link: 29245897
Variant Present in the following documents:
  • oncotarget-08-99237-s002.xlsx, sheet 1
View BVdb publication page



Novel de novo EEF1A2 missense mutations causing epilepsy and intellectual disability.

Molecular Genetics & Genomic Medicine
Lam, Wayne W K WW; Millichap, John J JJ; Soares, Dinesh C DC; Chin, Richard R; McLellan, Ailsa A; FitzPatrick, David R DR; Elmslie, Frances F; Lees, Melissa M MM; Schaefer, G Bradley GB; , ; Abbott, Catherine M CM
Publication Date: 2016-07

Variant appearance in text: 225: G364A
PubMed Link: 27441201
Variant Present in the following documents:
  • Main text
  • MGG3-4-465.pdf
View BVdb publication page



Characterization of DNA variants in the human kinome in breast cancer.

Scientific Reports
Agarwal, Divyansh D; Qi, Yuan Y; Jiang, Tingting T; Liu, Xiuping X; Shi, Weiwei W; Wali, Vikram B VB; Turk, Benjamin B; Ross, Jeffrey S JS; Fraser Symmans, W W; Pusztai, Lajos L; Hatzis, Christos C
Publication Date: 2015-09-30

Variant appearance in text: 225: G364A
PubMed Link: 26420498
Variant Present in the following documents:
  • srep14736-s2.xls, sheet 11
  • srep14736-s2.xls, sheet 8
View BVdb publication page