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EGFR c.1578C>G ;(p.C526W)
Variant ID: 7-55229271-C-G
NM_005228.3(
EGFR
):c.1578C>G;(p.C526W)
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:
Splitting p63.
American Journal Of Human Genetics
van Bokhoven, Hans H; Brunner, Han G HG
Publication Date: 2002-07
Variant appearance in text: EGFR: C526W
PubMed Link:
12037717
Variant Present in the following documents:
Main text
View BVdb publication page