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EGFR c.1444G>A ;(p.G482R)
Variant ID: 7-55227977-G-A
NM_005228.3(
EGFR
):c.1444G>A;(p.G482R)
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:
ErBb Family Proteins in Cholangiocarcinoma and Clinical Implications.
Journal Of Clinical Medicine
Jin, Wook W
Publication Date: 2020-07-16
Variant appearance in text: EGFR: G482R
PubMed Link:
32708604
Variant Present in the following documents:
Main text
jcm-09-02255.pdf
View BVdb publication page