EGF c.647G>A ;(p.W216*)

Variant ID: 4-110865135-G-A

NM_001963.4(EGF):c.647G>A;(p.W216*)

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:

Early Components of the Complement Classical Activation Pathway in Human Systemic Autoimmune Diseases.

Frontiers In Immunology
Lintner, Katherine E KE; Wu, Yee Ling YL; Yang, Yan Y; Spencer, Charles H CH; Hauptmann, Georges G; Hebert, Lee A LA; Atkinson, John P JP; Yu, C Yung CY
Publication Date: 2016

Variant appearance in text: EGF: W216X
PubMed Link: 26913032
Variant Present in the following documents:
  • Main text
  • fimmu-07-00036.pdf
View BVdb publication page