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KCNQ1 c.44_45delinsAT ;(p.W15Y)
Variant ID: 11-2466372-GG-AT
NM_000218.2(
KCNQ1
):c.44_45delinsAT;(p.W15Y)
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:
Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.
Forensic Sciences Research
Wu, Yeda Y; Ai, Mei M; Bardeesi, Adham Sameer A ASA; Xu, Lunwu L; Zheng, Jingjing J; Zheng, Da D; Yin, Kun K; Wu, Qiuping Q; Zhang, Liyong L; Huang, Lei L; Cheng, Jianding J
Publication Date: 2017
Variant appearance in text: KCNQ1: W15Y
PubMed Link:
30483629
Variant Present in the following documents:
Main text
tfsr-2-1333203.pdf
View BVdb publication page