LRP1B c.2813G>T ;(p.R938L)

Variant ID: 2-141739803-C-A

NM_018557.2(LRP1B):c.2813G>T;(p.R938L)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Predictive mutation signature of immunotherapy benefits in NSCLC based on machine learning algorithms.

Frontiers In Immunology
Liu, Zhichao Z; Lin, Guo G; Yan, Zeping Z; Li, Linduo L; Wu, Xingchen X; Shi, Jingrong J; He, Jianxing J; Zhao, Lei L; Liang, Hengrui H; Wang, Wei W
Publication Date: 2022

Variant appearance in text: LRP1B: 2813G>T; R938L
PubMed Link: 36238300
Variant Present in the following documents:
  • Table_1.xlsx, sheet 4
View BVdb publication page



EPHA5 mutation was associated with adverse outcome of atezolizumab treatment in late-stage non-small cell lung cancers.

Bmc Pulmonary Medicine
Li, Zhenxiang Z; Zhou, Qing Q; Wang, Qi Q; Wang, Haiyong H; Yue, Weiming W
Publication Date: 2022-09-19

Variant appearance in text: LRP1B: 2813G>T; R938L
PubMed Link: 36123678
Variant Present in the following documents:
  • 12890_2022_2161_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genomic Alterations Identification and Resistance Mechanisms Exploration of NSCLC With Central Nervous System Metastases Using Liquid Biopsy of Cerebrospinal Fluid: A Real-World Study.

Frontiers In Oncology
Shen, Fangfang F; Liang, Naixin N; Fan, Zaiwen Z; Zhao, Min M; Kang, Jing J; Wang, Xifang X; Hu, Qun Q; Mu, Yongping Y; Wang, Kai K; Yuan, Mingming M; Chen, Rongrong R; Guo, Wei W; Dong, Guilan G; Zhao, Jun J; Bai, Jun J
Publication Date: 2022

Variant appearance in text: LRP1B: 2813G>T; R938L
PubMed Link: 35814426
Variant Present in the following documents:
  • DataSheet_1.xlsx, sheet 2
View BVdb publication page



EM-mosaic detects mosaic point mutations that contribute to congenital heart disease.

Genome Medicine
Hsieh, Alexander A; Morton, Sarah U SU; Willcox, Jon A L JAL; Gorham, Joshua M JM; Tai, Angela C AC; Qi, Hongjian H; DePalma, Steven S; McKean, David D; Griffin, Emily E; Manheimer, Kathryn B KB; Bernstein, Daniel D; Kim, Richard W RW; Newburger, Jane W JW; Porter, George A GA; Srivastava, Deepak D; Tristani-Firouzi, Martin M; Brueckner, Martina M; Lifton, Richard P RP; Goldmuntz, Elizabeth E; Gelb, Bruce D BD; Chung, Wendy K WK; Seidman, Christine E CE; Seidman, J G JG; Shen, Yufeng Y
Publication Date: 2020-04-29

Variant appearance in text: LRP1B: R938L
PubMed Link: 32349777
Variant Present in the following documents:
  • 13073_2020_738_MOESM1_ESM.xlsx, sheet 4
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: LRP1B: 2813G>T; R938L
PubMed Link: 31925297
Variant Present in the following documents:
  • 42003_2019_736_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page