CD36 c.1399A>G ;(p.R467G)

Variant ID: 7-80303443-A-G

NM_001001548.2(CD36):c.1399A>G;(p.R467G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours.

Orphanet Journal Of Rare Diseases
Barclay, Sarah F SF; Rand, Casey M CM; Borch, Lauren A LA; Nguyen, Lisa L; Gray, Paul A PA; Gibson, William T WT; Wilson, Richard J A RJ; Gordon, Paul M K PM; Aung, Zaw Z; Berry-Kravis, Elizabeth M EM; Ize-Ludlow, Diego D; Weese-Mayer, Debra E DE; Bech-Hansen, N Torben NT
Publication Date: 2015-08-25

Variant appearance in text: CD36: 1399A>G; R467G
PubMed Link: 26302956
Variant Present in the following documents:
  • Main text
  • 13023_2015_Article_314.pdf
  • 13023_2015_314_MOESM1_ESM.xlsx, sheet 5
  • 13023_2015_314_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page