Bibliome.ai browser hg19
Search
About
Stats
FAQ
SCN1A c.788T>A ;(p.L263Q)
Variant ID: 2-166908405-A-T
NM_001165963.1(
SCN1A
):c.788T>A;(p.L263Q)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Epilepsy and migraine-Are they comorbidity?
Genes & Diseases
Liao, Jin J; Tian, Xin X; Wang, Hao H; Xiao, Zheng Z
Publication Date: 2018-06
Variant appearance in text: SCN1A: L263Q
PubMed Link:
30258939
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page
Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
Cephalalgia : An International Journal Of Headache
Fan, Chunxiang C; Wolking, Stefan S; Lehmann-Horn, Frank F; Hedrich, Ulrike Bs UB; Freilinger, Tobias T; Lerche, Holger H; Borck, Guntram G; Kubisch, Christian C; Jurkat-Rott, Karin K
Publication Date: 2016-11
Variant appearance in text: SCN1A: L263Q
PubMed Link:
26763045
Variant Present in the following documents:
Main text
10.1177_0333102415608360.pdf
View BVdb publication page