GRIN2A c.2890C>G ;(p.Q964E)

Variant ID: 16-9858511-G-C

NM_001134407.1(GRIN2A):c.2890C>G;(p.Q964E)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.

Translational Psychiatry
Yu, Yanjie Y; Lin, Yingni Y; Takasaki, Yuto Y; Wang, Chenyao C; Kimura, Hiroki H; Xing, Jingrui J; Ishizuka, Kanako K; Toyama, Miho M; Kushima, Itaru I; Mori, Daisuke D; Arioka, Yuko Y; Uno, Yota Y; Shiino, Tomoko T; Nakamura, Yukako Y; Okada, Takashi T; Morikawa, Mako M; Ikeda, Masashi M; Iwata, Nakao N; Okahisa, Yuko Y; Takaki, Manabu M; Sakamoto, Shinji S; Someya, Toshiyuki T; Egawa, Jun J; Usami, Masahide M; Kodaira, Masaki M; Yoshimi, Akira A; Oya-Ito, Tomoko T; Aleksic, Branko B; Ohno, Kinji K; Ozaki, Norio N
Publication Date: 2018-01-10

Variant appearance in text: GRIN2A: Q964E
PubMed Link: 29317596
Variant Present in the following documents:
  • Main text
  • 41398_2017_Article_61.pdf
View BVdb publication page