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