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TNNT2 c.199+258C>T
Variant ID: 1-201336641-G-A
NM_001276345.1(
TNNT2
):c.199+258C>T
This variant was identified in 4 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.
Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018
Variant appearance in text: TNNT2: 199+258C>T; rs1892028
PubMed Link:
30319441
Variant Present in the following documents:
Table_5.xlsx, sheet 1
Table_6.xlsx, sheet 1
View BVdb publication page
Identification of a single nucleotide polymorphism indicative of high risk in acute myocardial infarction.
The Indian Journal Of Medical Research
Shalia, Kavita K; Saranath, Dhananjaya D; Rayar, Jaipreet J; Shah, Vinod K VK; Mashru, Manoj R MR; Soneji, Surendra L SL
Publication Date: 2017-10
Variant appearance in text: rs1892028
PubMed Link:
29434065
Variant Present in the following documents:
Main text
IJMR-146-505.pdf
View BVdb publication page
Cardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patients.
Biomed Research International
Li, Xiaoping X; Luo, Rong R; Gu, Haiyong H; Deng, Yun Y; Xu, Xiaolei X; Wu, Xiushan X; Hua, Wei W
Publication Date: 2014
Variant appearance in text: rs1892028
PubMed Link:
25110706
Variant Present in the following documents:
Main text
BMRI2014-907360.pdf
View BVdb publication page
TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.
Biomed Research International
Li, Xiaoping X; Wang, Huan H; Luo, Rong R; Gu, Haiyong H; Zhang, Channa C; Zhang, Yu Y; Hui, Rutai R; Wu, Xiushan X; Hua, Wei W
Publication Date: 2013
Variant appearance in text: rs1892028
PubMed Link:
23586019
Variant Present in the following documents:
Main text
BMRI2013-201372.pdf
View BVdb publication page