SLC2A9 c.1375T>A ;(p.W459R)

Variant ID: 4-9836549-A-T

NM_020041.2(SLC2A9):c.1375T>A;(p.W459R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.

Nature Communications
Cirulli, Elizabeth T ET; White, Simon S; Read, Robert W RW; Elhanan, Gai G; Metcalf, William J WJ; Tanudjaja, Francisco F; Fath, Donna M DM; Sandoval, Efren E; Isaksson, Magnus M; Schlauch, Karen A KA; Grzymski, Joseph J JJ; Lu, James T JT; Washington, Nicole L NL
Publication Date: 2020-01-28

Variant appearance in text: SLC2A9: W459R
PubMed Link: 31992710
Variant Present in the following documents:
  • 41467_2020_Article_14288.pdf
View BVdb publication page