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EGFR c.1381G>C ;(p.V461L)
Variant ID: 7-55227914-G-C
NM_005228.3(
EGFR
):c.1381G>C;(p.V461L)
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:
Oncogene Mutation Survey in MPNST Cell Lines Enhances the Dominant Role of Hyperactive Ras in NF1 Associated Pro-Survival and Malignancy.
Translational Oncogenomics
Sun, Daochun D; Tainsky, Michael A MA; Haddad, Ramsi R
Publication Date: 2012
Variant appearance in text: EGFR: V461L
PubMed Link:
22346343
Variant Present in the following documents:
Main text
View BVdb publication page