GRIN2A c.2007+1G>A

Variant ID: 16-9923279-C-T

NM_001134407.1(GRIN2A):c.2007+1G>A

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy.

Neuroscience Bulletin
Xu, Xing-Xing XX; Luo, Jian-Hong JH
Publication Date: 2018-06

Variant appearance in text: GRIN2A: 2007+1G>A
PubMed Link: 29124671
Variant Present in the following documents:
  • Main text
View BVdb publication page


Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.

Neuroscience Bulletin
Wei, Feng F; Yan, Li-Min LM; Su, Tao T; He, Na N; Lin, Zhi-Jian ZJ; Wang, Jie J; Shi, Yi-Wu YW; Yi, Yong-Hong YH; Liao, Wei-Ping WP
Publication Date: 2017-08

Variant appearance in text: GRIN2A: 2007+1G>A
PubMed Link: 28488083
Variant Present in the following documents:
  • Main text
View BVdb publication page