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SCN1A c.1006T>G ;(p.C336G)
Variant ID: 2-166905418-A-C
NM_001165963.1(
SCN1A
):c.1006T>G;(p.C336G)
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:
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Molecular Neurobiology
Zhang, Yi Y; Wang, Tao T; Wang, Yan Y; Xia, Kun K; Li, Jinchen J; Sun, Zhongsheng Z
Publication Date: 2021-08
Variant appearance in text: SCN1A: 1006T>G; C336G
PubMed Link:
33860439
Variant Present in the following documents:
12035_2021_2377_MOESM14_ESM.xlsx, sheet 1
View BVdb publication page