GRIN2A c.3059C>G ;(p.S1020C)

Variant ID: 16-9858342-G-C

NM_001134407.1(GRIN2A):c.3059C>G;(p.S1020C)

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:

Next-Generation Sequencing in Korean Children With Autism Spectrum Disorder and Comorbid Epilepsy.

Frontiers In Pharmacology
Lee, Junghan J; Ha, Sungji S; Lee, Seung-Tae ST; Park, Sung-Gyun SG; Shin, Saeam S; Choi, Jong Rak JR; Cheon, Keun-Ah KA
Publication Date: 2020

Variant appearance in text: GRIN2A: 3059C>G; Ser1020Cys
PubMed Link: 32477112
Variant Present in the following documents:
  • Main text
  • fphar-11-00585.pdf
View BVdb publication page