EGF c.628C>T ;(p.L210F)

Variant ID: 4-110865116-C-T

NM_001963.4(EGF):c.628C>T;(p.L210F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multigene Panel Sequencing Reveals Cancer-Specific and Common Somatic Mutations in Colorectal Cancer Patients: An Egyptian Experience.

Current Issues In Molecular Biology
Youssef, Amira Salah El-Din ASE; Abdel-Fattah, Mohamed A MA; Lotfy, Mai M MM; Nassar, Auhood A; Abouelhoda, Mohamed M; Touny, Ahmed O AO; Hassan, Zeinab K ZK; Mohey Eldin, Mohammed M; Bahnassy, Abeer A AA; Khaled, Hussein H; Zekri, Abdel Rahman N ARN
Publication Date: 2022-03-18

Variant appearance in text: EGF: 628C>T
PubMed Link: 35723313
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon.

International Journal Of Molecular Sciences
Nadarajah, Noeline N; Schulte, Dörte D; McConnell, Vivienne V; Martin-Almedina, Silvia S; Karapouliou, Christina C; Mortimer, Peter S PS; Jeffery, Steve S; Schulte-Merker, Stefan S; Gordon, Kristiana K; Mansour, Sahar S; Ostergaard, Pia P
Publication Date: 2018-08-01

Variant appearance in text: EGF: 628C>T
PubMed Link: 30071673
Variant Present in the following documents:
  • Main text
  • ijms-19-02259.pdf
View BVdb publication page