SCN1A c.3740_3751del ;(p.T1247_T1250del)

Variant ID: 2-166868746-ATCGTCTTAATCG-A

NM_001165963.1(SCN1A):c.3740_3751del;(p.T1247_T1250del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A.

Frontiers In Molecular Neuroscience
Wang, Jing-Yang JY; Tang, Bin B; Sheng, Wen-Xiang WX; Hua, Li-Dong LD; Zeng, Yang Y; Fan, Cui-Xia CX; Deng, Wei-Yi WY; Gao, Mei-Mei MM; Zhu, Wei-Wen WW; He, Na N; Su, Tao T
Publication Date: 2022

Variant appearance in text: SCN1A: Thr1247_Thr1250del
PubMed Link: 35359575
Variant Present in the following documents:
  • Main text
  • fnmol-15-828846.pdf
View BVdb publication page