GRIN2A c.2600T>C ;(p.I867T)

Variant ID: 16-9858801-A-G

NM_001134407.1(GRIN2A):c.2600T>C;(p.I867T)

This variant was identified in 1 publication

View GRCh38 version.



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

Publications:

Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses.

Frontiers In Molecular Neuroscience
Won, Hyejung H; Mah, Won W; Kim, Eunjoon E
Publication Date: 2013

Variant appearance in text: GluN2A: I867T
PubMed Link: 23935565
Variant Present in the following documents:
  • Main text
  • fnmol-06-00019.pdf
View BVdb publication page