Bibliome.ai browser hg19
Search
About
Stats
FAQ
ERBB2 c.146T>G ;(p.L49R)
Variant ID: 17-37863315-T-G
NM_004448.2(
ERBB2
):c.146T>G;(p.L49R)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Identifying Actionable Variants Using Capture-Based Targeted Sequencing in 563 Patients With Non-Small Cell Lung Carcinoma.
Frontiers In Oncology
Jiang, Haiping H; Wang, Yinan Y; Xu, Hanlin H; Lei, Wei W; Yu, Xiaoyun X; Tian, Haiying H; Meng, Cong C; Wang, Xueying X; Zhao, Zicheng Z; Jin, Xiangfeng X
Publication Date: 2021
Variant appearance in text: ERBB2: L49R
PubMed Link:
35186718
Variant Present in the following documents:
Table_1.xlsx, sheet 2
View BVdb publication page
Rigidity of the extracellular part of HER2: Evidence from engineering subdomain interfaces and shared-helix DARPin-DARPin fusions.
Protein Science : A Publication Of The Protein Society
Jost, Christian C; Stüber, Jakob C JC; Honegger, Annemarie A; Wu, Yufan Y; Batyuk, Alexander A; Plückthun, Andreas A
Publication Date: 2017-09
Variant appearance in text: HER2: L49R
PubMed Link:
28639341
Variant Present in the following documents:
Main text
View BVdb publication page