SCN1A c.4198del ;(p.I1400*)

Variant ID: 2-166859067-AT-A

NM_001165963.1(SCN1A):c.4198del;(p.I1400*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy.

Frontiers In Neurology
Demos, Michelle M; Guella, Ilaria I; DeGuzman, Conrado C; McKenzie, Marna B MB; Buerki, Sarah E SE; Evans, Daniel M DM; Toyota, Eric B EB; Boelman, Cyrus C; Huh, Linda L LL; Datta, Anita A; Michoulas, Aspasia A; Selby, Kathryn K; Bjornson, Bruce H BH; Horvath, Gabriella G; Lopez-Rangel, Elena E; van Karnebeek, Clara D M CDM; Salvarinova, Ramona R; Slade, Erin E; Eydoux, Patrice P; Adam, Shelin S; Van Allen, Margot I MI; Nelson, Tanya N TN; Bolbocean, Corneliu C; Connolly, Mary B MB; Farrer, Matthew J MJ
Publication Date: 2019

Variant appearance in text: SCN1A: 4198delA; I1400X
PubMed Link: 31164858
Variant Present in the following documents:
  • Main text
  • fneur-10-00434.pdf
View BVdb publication page