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KCNQ1 c.386+30787C>T
Variant ID: 11-2497501-C-T
NM_000218.2(
KCNQ1
):c.386+30787C>T
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:
The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.
Frontiers In Cellular Neuroscience
Chen, Xue-Min XM; Xue, Xin-Miao XM; Yu, Ning N; Guo, Wei-Wei WW; Yuan, Shuo-Long SL; Jiang, Qing-Qing QQ; Yang, Shi-Ming SM
Publication Date: 2022
Variant appearance in text: rs718579
PubMed Link:
35903368
Variant Present in the following documents:
Main text
fncel-16-946206.pdf
View BVdb publication page
Noise-Induced Hearing Loss: Updates on Molecular Targets and Potential Interventions.
Neural Plasticity
Mao, Huanyu H; Chen, Yan Y
Publication Date: 2021
Variant appearance in text: rs718579
PubMed Link:
34306060
Variant Present in the following documents:
Main text
NP2021-4784385.pdf
View BVdb publication page
Modeling susceptibility to drug-induced long QT with a panel of subject-specific induced pluripotent stem cells.
Elife
Stillitano, Francesca F; Hansen, Jens J; Kong, Chi-Wing CW; Karakikes, Ioannis I; Funck-Brentano, Christian C; Geng, Lin L; Scott, Stuart S; Reynier, Stephan S; Wu, Ma M; Valogne, Yannick Y; Desseaux, Carole C; Salem, Joe-Elie JE; Jeziorowska, Dorota D; Zahr, Noël N; Li, Ronald R; Iyengar, Ravi R; Hajjar, Roger J RJ; Hulot, Jean-Sébastien JS
Publication Date: 2017-01-30
Variant appearance in text: rs718579
PubMed Link:
28134617
Variant Present in the following documents:
Main text
elife-19406.pdf
View BVdb publication page