SCN1A c.4985_4989del ;(p.A1662Dfs*9)

Variant ID: 2-166848795-TCAAAG-T

NM_001165963.1(SCN1A):c.4985_4989del;(p.A1662Dfs*9)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Data on mutations and Clinical features in SCN1A or SCN2A gene.

Data In Brief
Kong, Yanting Y; Yan, Kai K; Hu, Liyuan L; Wang, Mingbang M; Dong, Xinran X; Lu, Yulan Y; Wu, Bingbing B; Wang, Huijun H; Yang, Lin L; Zhou, Wenhao W
Publication Date: 2019-02

Variant appearance in text: SCN1A: 4985_4989delCTTTG
PubMed Link: 30619928
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page