EGFR c.1550G>C ;(p.G517A)

Variant ID: 7-55229243-G-C

NM_005228.3(EGFR):c.1550G>C;(p.G517A)

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:

Neurofibromin 1 (NF1) defects are common in human ovarian serous carcinomas and co-occur with TP53 mutations.

Neoplasia (New York, N.Y.)
Sangha, Navneet N; Wu, Rong R; Kuick, Rork R; Powers, Scott S; Mu, David D; Fiander, Diane D; Yuen, Kit K; Katabuchi, Hidetaka H; Tashiro, Hironori H; Fearon, Eric R ER; Cho, Kathleen R KR
Publication Date: 2008-12

Variant appearance in text: EGFR: G517A
PubMed Link: 19048115
Variant Present in the following documents:
  • Main text
View BVdb publication page