APOE c.299T>C ;(p.L100P)

Variant ID: 19-45411852-T-C

NM_000041.2(APOE):c.299T>C;(p.L100P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Functional brain defects in a mouse model of a chromosomal t(1;11) translocation that disrupts DISC1 and confers increased risk of psychiatric illness.

Translational Psychiatry
Bonneau, Marion M; Sullivan, Shane T O' STO; Gonzalez-Lozano, Miguel A MA; Baxter, Paul P; Gautier, Phillippe P; Marchisella, Elena E; Hardingham, Neil R NR; Chesters, Robert A RA; Torrance, Helen H; Howard, David M DM; Jansen, Maurits A MA; McMillan, Melanie M; Singh, Yasmin Y; Didier, Michel M; Koopmans, Frank F; Semple, Colin A CA; McIntosh, Andrew M AM; Volkmer, Hansjürgen H; Loos, Maarten M; Fox, Kevin K; Hardingham, Giles E GE; Vernon, Anthony C AC; Porteous, David J DJ; Smit, August B AB; Price, David J DJ; Kirsty Millar, J J
Publication Date: 2021-02-19

Variant appearance in text: APOE: L100P
PubMed Link: 33608504
Variant Present in the following documents:
  • 41398_2021_Article_1256.pdf
View BVdb publication page