EGFR c.599G>T ;(p.W200L)

Variant ID: 7-55219026-G-T

NM_005228.3(EGFR):c.599G>T;(p.W200L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast Cancer.

Biomedicines
Liu, Yaxuan Y; Helgadottir, Hafdis T HT; Kharaziha, Pedram P; Choi, Jungmin J; López-Giráldez, Francesc F; Mane, Shrikant M SM; Höiom, Veronica V; Juhlin, Carl Christofer CC; Larsson, Catharina C; Bajalica-Lagercrantz, Svetlana S
Publication Date: 2022-04-26

Variant appearance in text: EGFR: 599G>T; W200L
PubMed Link: 35625741
Variant Present in the following documents:
  • biomedicines-10-01004.pdf
View BVdb publication page



Pan-cancer circulating tumor DNA detection in over 10,000 Chinese patients.

Nature Communications
Zhang, Yongliang Y; Yao, Yu Y; Xu, Yaping Y; Li, Lifeng L; Gong, Yan Y; Zhang, Kai K; Zhang, Meng M; Guan, Yanfang Y; Chang, Lianpeng L; Xia, Xuefeng X; Li, Lin L; Jia, Shuqin S; Zeng, Qiang Q
Publication Date: 2021-01-04

Variant appearance in text: EGFR: 599G>T; W200L
PubMed Link: 33397889
Variant Present in the following documents:
  • 41467_2020_20162_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page