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SCN4B c.616_617delinsAA ;(p.S206K)
Variant ID: 11-118007812-GA-TT
NM_174934.3(
SCN4B
):c.616_617delinsAA;(p.S206K)
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:
Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia.
Molecular Genetics And Genomics : Mgg
Yang, Qin Q; Xiong, Hongbo H; Xu, Chengqi C; Huang, Yuan Y; Tu, Xin X; Wu, Gang G; Fu, Fenfen F; Wang, Zhijie Z; Wang, Longfei L; Zhao, Yuanyuan Y; Li, Sisi S; Huang, Yufeng Y; Wang, Chuchu C; Wang, Dan D; Yao, Yufeng Y; Wang, Fan F; Wang, Yongbo Y; Xue, Yu Y; Wang, Pengyun P; Chen, Qiuyun Q; Pu, Jielin J; Wang, Qing K QK
Publication Date: 2019-08
Variant appearance in text: SCN4B: Ser206Lys
PubMed Link:
31020414
Variant Present in the following documents:
Main text
View BVdb publication page