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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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