SCN1A c.332T>A ;(p.L111*)

Variant ID: 2-166915131-A-T

NM_001165963.1(SCN1A):c.332T>A;(p.L111*)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disorders.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics
Stosser, Mary Beth MB; Lindy, Amanda S AS; Butler, Elizabeth E; Retterer, Kyle K; Piccirillo-Stosser, Caitlin M CM; Richard, Gabriele G; McKnight, Dianalee A DA
Publication Date: 2018-04

Variant appearance in text: SCN1A: 332T>A
PubMed Link: 28837158
Variant Present in the following documents:
  • Main text
  • gim2017114a.pdf
View BVdb publication page