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WNK4 c.1184A>C ;(p.N395T)
Variant ID: 17-40937128-A-C
NM_032387.4(
WNK4
):c.1184A>C;(p.N395T)
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:
Genetic screening for monogenic hypertension in hypertensive individuals in a clinical setting.
Journal Of Medical Genetics
Bao, Minghui M; Li, Ping P; Li, Qifu Q; Chen, Hui H; Zhong, Ying Y; Li, Shuangyue S; Jin, Ling L; Wang, Wenjie W; Chen, Zhenzhen Z; Zhong, Jiuchang J; Geng, Bin B; Fan, Yuxin Y; Yang, Xinchun X; Cai, Jun J
Publication Date: 2020-08
Variant appearance in text: WNK4: N395T
PubMed Link:
32561571
Variant Present in the following documents:
jmedgenet-2019-106145supp001.pdf
View BVdb publication page