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KCTD10 c.*808G>A
Variant ID: 12-109888592-C-T
NM_031954.3(
KCTD10
):c.*808G>A
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:
Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.
Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11
Variant appearance in text: rs7295954
PubMed Link:
32046637
Variant Present in the following documents:
12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page
Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population.
Lipids In Health And Disease
Sun, Jie J; Qian, Yun Y; Jiang, Yue Y; Chen, Jiaping J; Dai, Juncheng J; Jin, Guangfu G; Wang, Jianming J; Hu, Zhibin Z; Liu, Sijun S; Shen, Chong C; Shen, Hongbing H
Publication Date: 2016-10-04
Variant appearance in text: rs7295954
PubMed Link:
27716295
Variant Present in the following documents:
Main text
12944_2016_Article_348.pdf
View BVdb publication page