EGFR c.1366A>G ;(p.I456V)

Variant ID: 7-55227899-A-G

NM_005228.3(EGFR):c.1366A>G;(p.I456V)

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:

An In Silico Evaluation of Deleterious Nonsynonymous Single Nucleotide Polymorphisms in the ErbB3 Oncogene.

Bioresearch Open Access
Raghav, Dhwani D; Sharma, Vinay V
Publication Date: 2013-06

Variant appearance in text: EGFR: I456V
PubMed Link: 23741632
Variant Present in the following documents:
  • Main text
View BVdb publication page