LRP1B c.2690G>A ;(p.R897H)

Variant ID: 2-141747181-C-T

NM_018557.2(LRP1B):c.2690G>A;(p.R897H)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


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: 2690G>A; R897H
PubMed Link: 35814426
Variant Present in the following documents:
  • DataSheet_1.xlsx, sheet 2
View BVdb publication page



Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation.

Cell Stem Cell
Merkle, Florian T FT; Ghosh, Sulagna S; Genovese, Giulio G; Handsaker, Robert E RE; Kashin, Seva S; Meyer, Daniel D; Karczewski, Konrad J KJ; O'Dushlaine, Colm C; Pato, Carlos C; Pato, Michele M; MacArthur, Daniel G DG; McCarroll, Steven A SA; Eggan, Kevin K
Publication Date: 2022-03-03

Variant appearance in text: LRP1B: 2690G>A; R897H
PubMed Link: 35176222
Variant Present in the following documents:
  • mmc5.xlsx, sheet 3
View BVdb publication page



Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium.

Scientific Reports
Popp, Bernt B; Krumbiegel, Mandy M; Grosch, Janina J; Sommer, Annika A; Uebe, Steffen S; Kohl, Zacharias Z; Plötz, Sonja S; Farrell, Michaela M; Trautmann, Udo U; Kraus, Cornelia C; Ekici, Arif B AB; Asadollahi, Reza R; Regensburger, Martin M; Günther, Katharina K; Rauch, Anita A; Edenhofer, Frank F; Winkler, Jürgen J; Winner, Beate B; Reis, André A
Publication Date: 2018-11-21

Variant appearance in text: LRP1B: 2690G>A; Arg897His; rs763519057
PubMed Link: 30464253
Variant Present in the following documents:
  • 41598_2018_35506_MOESM5_ESM.xlsx, sheet 4
View BVdb publication page



NOTCH1 pathway activating mutations and clonal evolution in pediatric T-cell acute lymphoblastic leukemia.

Cancer Science
Kimura, Shunsuke S; Seki, Masafumi M; Yoshida, Kenichi K; Shiraishi, Yuichi Y; Akiyama, Masaharu M; Koh, Katsuyoshi K; Imamura, Toshihiko T; Manabe, Atsushi A; Hayashi, Yasuhide Y; Kobayashi, Masao M; Oka, Akira A; Miyano, Satoru S; Ogawa, Seishi S; Takita, Junko J
Publication Date: 2019-02

Variant appearance in text: LRP1B: R897H
PubMed Link: 30387229
Variant Present in the following documents:
  • CAS-110-784-s012.xlsx, sheet 1
View BVdb publication page



Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing.

Nature Communications
Nahar, Rahul R; Zhai, Weiwei W; Zhang, Tong T; Takano, Angela A; Khng, Alexis J AJ; Lee, Yin Yeng YY; Liu, Xingliang X; Lim, Chong Hee CH; Koh, Tina P T TPT; Aung, Zaw Win ZW; Lim, Tony Kiat Hon TKH; Veeravalli, Lavanya L; Yuan, Ju J; Teo, Audrey S M ASM; Chan, Cheryl X CX; Poh, Huay Mei HM; Chua, Ivan M L IML; Liew, Audrey Ann AA; Lau, Dawn Ping Xi DPX; Kwang, Xue Lin XL; Toh, Chee Keong CK; Lim, Wan-Teck WT; Lim, Bing B; Tam, Wai Leong WL; Tan, Eng-Huat EH; Hillmer, Axel M AM; Tan, Daniel S W DSW
Publication Date: 2018-01-15

Variant appearance in text: LRP1B: R897H
PubMed Link: 29335443
Variant Present in the following documents:
  • 41467_2017_2584_MOESM4_ESM.xlsx, sheet 15
  • 41467_2017_2584_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page