EGFR c.229T>G ;(p.S77A)

Variant ID: 7-55210119-T-G

NM_005228.3(EGFR):c.229T>G;(p.S77A)

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:

A phosphorylation defective retinoic acid receptor mutant mimics the effects of retinoic acid on EGFR mediated AP-1 expression and cancer cell proliferation.

Cancer Cell International
Crowe, David L DL; Kim, Randie R
Publication Date: 2002-10-08

Variant appearance in text: EGFR: S77A
PubMed Link: 12392597
Variant Present in the following documents:
  • Main text
  • 1475-2867-2-15.pdf
View BVdb publication page