SCN1A c.1254C>G ;(p.I418M)

Variant ID: 2-166903403-G-C

NM_001165963.1(SCN1A):c.1254C>G;(p.I418M)

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:

Exome sequencing of Japanese schizophrenia multiplex families supports the involvement of calcium ion channels.

Plos One
Toyama, Miho M; Takasaki, Yuto Y; Branko, Aleksic A; Kimura, Hiroki H; Kato, Hidekazu H; Nawa, Yoshihiro Y; Kushima, Itaru I; Ishizuka, Kanako K; Shimamura, Teppei T; Ogi, Tomoo T; Ozaki, Norio N
Publication Date: 2022

Variant appearance in text: SCN1A: I418M
PubMed Link: 35536790
Variant Present in the following documents:
  • pone.0268321.s003.xlsx, sheet 1
View BVdb publication page