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EGFR c.1699A>G ;(p.M567V)
Variant ID: 7-55231493-A-G
NM_005228.3(
EGFR
):c.1699A>G;(p.M567V)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Investigation of PALB2 Mutation and Correlation With Immunotherapy Biomarker in Chinese Non-Small Cell Lung Cancer Patients.
Frontiers In Oncology
Zhang, Jiexia J; Tang, Shuangfeng S; Zhang, Chunning C; Li, Mingyao M; Zheng, Yating Y; Hu, Xue X; Huang, Mengli M; Cheng, Xiangyang X
Publication Date: 2021
Variant appearance in text: EGFR: 1699A>G; M567V
PubMed Link:
35087742
Variant Present in the following documents:
Table_2.xlsx, sheet 1
View BVdb publication page