SCN1A c.35A>G ;(p.D12G)

Variant ID: 2-166930097-T-C

NM_001165963.1(SCN1A):c.35A>G;(p.D12G)

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:

Genetic Factors in Rasmussen's Encephalitis Characterized by Whole-Exome Sequencing.

Frontiers In Neuroscience
Ai, Junhong J; Wang, Yisong Y; Liu, Dong D; Fan, Dongying D; Wang, Qiqi Q; Li, Tianfu T; Luan, Guoming G; Wang, Peigang P; An, Jing J
Publication Date: 2021

Variant appearance in text: SCN1A: 35A>G; Asp12Gly
PubMed Link: 34675770
Variant Present in the following documents:
  • fnins-15-744429.pdf
View BVdb publication page