PRKCE c.349-20103G>A

Variant ID: 2-46050036-G-A

NM_005400.2(PRKCE):c.349-20103G>A

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:

Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.

Human Mutation
Paré-Brunet, Laia L; Glubb, Dylan D; Evans, Patrick P; Berenguer-Llergo, Antoni A; Etheridge, Amy S AS; Skol, Andrew D AD; Di Rienzo, Anna A; Duan, Shiwei S; Gamazon, Eric R ER; Innocenti, Federico F
Publication Date: 2014-02

Variant appearance in text: rs7559522
PubMed Link: 24186849
Variant Present in the following documents:
  • Main text
View BVdb publication page