CD36 c.1176G>T ;(p.L392F)

Variant ID: 7-80302136-G-T

NM_001001548.2(CD36):c.1176G>T;(p.L392F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.

Genome Biology
Jansen, Iris E IE; Ye, Hui H; Heetveld, Sasja S; Lechler, Marie C MC; Michels, Helen H; Seinstra, Renée I RI; Lubbe, Steven J SJ; Drouet, Valérie V; Lesage, Suzanne S; Majounie, Elisa E; Gibbs, J Raphael JR; Nalls, Mike A MA; Ryten, Mina M; Botia, Juan A JA; Vandrovcova, Jana J; Simon-Sanchez, Javier J; Castillo-Lizardo, Melissa M; Rizzu, Patrizia P; Blauwendraat, Cornelis C; Chouhan, Amit K AK; Li, Yarong Y; Yogi, Puja P; Amin, Najaf N; van Duijn, Cornelia M CM; , ; Morris, Huw R HR; Brice, Alexis A; Singleton, Andrew B AB; David, Della C DC; Nollen, Ellen A EA; Jain, Shushant S; Shulman, Joshua M JM; Heutink, Peter P
Publication Date: 2017-01-30

Variant appearance in text: CD36: 1176G>T; L392F
PubMed Link: 28137300
Variant Present in the following documents:
  • Main text
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