EGF c.2318A>G ;(p.K773R)

Variant ID: 4-110902078-A-G

NM_001963.4(EGF):c.2318A>G;(p.K773R)

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:

Loss of flotillin expression results in weakened desmosomal adhesion and Pemphigus vulgaris-like localisation of desmoglein-3 in human keratinocytes.

Scientific Reports
Völlner, Frauke F; Ali, Jawahir J; Kurrle, Nina N; Exner, Yvonne Y; Eming, Rüdiger R; Hertl, Michael M; Banning, Antje A; Tikkanen, Ritva R
Publication Date: 2016-06-27

Variant appearance in text: EGF: Lys773Arg
PubMed Link: 27346727
Variant Present in the following documents:
  • Main text
  • srep28820.pdf
View BVdb publication page