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KCNH2 c.211G>T ;(p.G71W)
Variant ID: 7-150671895-C-A
NM_000238.3(
KCNH2
):c.211G>T;(p.G71W)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A case of long QT syndrome type 2 that developed torsades de pointes two days after the initiation of oral β-blocker therapy.
Heartrhythm Case Reports
Yoneda, Fumiya F; Makiyama, Takeru T; Miyahara, Kosuke K; Fukuoka, Yoshitomo Y; Aiba, Takeshi T; Kimura, Takeshi T
Publication Date: 2022-11
Variant appearance in text: KCNH2: 211G>T
PubMed Link:
36618596
Variant Present in the following documents:
Main text
main.pdf
View BVdb publication page
Territory-Wide Chinese Cohort of Long QT Syndrome: Random Survival Forest and Cox Analyses.
Frontiers In Cardiovascular Medicine
Tse, Gary G; Lee, Sharen S; Zhou, Jiandong J; Liu, Tong T; Wong, Ian Chi Kei ICK; Mak, Chloe C; Mok, Ngai Shing NS; Jeevaratnam, Kamalan K; Zhang, Qingpeng Q; Cheng, Shuk Han SH; Wong, Wing Tak WT
Publication Date: 2021
Variant appearance in text: KCNH2: 211G>T
PubMed Link:
33614747
Variant Present in the following documents:
Main text
fcvm-08-608592.pdf
View BVdb publication page
Structures Illuminate Cardiac Ion Channel Functions in Health and in Long QT Syndrome.
Frontiers In Pharmacology
Brewer, Kathryn R KR; Kuenze, Georg G; Vanoye, Carlos G CG; George, Alfred L AL; Meiler, Jens J; Sanders, Charles R CR
Publication Date: 2020
Variant appearance in text: LQT2: G71W
PubMed Link:
32431610
Variant Present in the following documents:
Main text
fphar-11-00550.pdf
View BVdb publication page