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EGFR c.2149G>T ;(p.V717L)
Variant ID: 7-55241701-G-T
NM_005228.3(
EGFR
):c.2149G>T;(p.V717L)
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:
Next-Generation Sequencing Reveals High Uncommon EGFR Mutations and Tumour Mutation Burden in a Subgroup of Lung Cancer Patients.
Frontiers In Oncology
Guo, Gang G; Li, Gaofeng G; Liu, Yinqiang Y; Li, Heng H; Guo, Qi Q; Liu, Jun J; Yang, Xiumei X; Shou, Tao T; Shi, Yunfei Y
Publication Date: 2021
Variant appearance in text: EGFR: V717L
PubMed Link:
33889543
Variant Present in the following documents:
Main text
View BVdb publication page