TNNT2 c.253G>T ;(p.V85L)

Variant ID: 1-201334779-C-A

NM_001276345.1(TNNT2):c.253G>T;(p.V85L)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Prognostic implications of troponin T variations in inherited cardiomyopathies using systems biology.

Npj Genomic Medicine
Shakur, Rameen R; Ochoa, Juan Pablo JP; Robinson, Alan J AJ; Niroula, Abhishek A; Chandran, Aneesh A; Rahman, Taufiq T; Vihinen, Mauno M; Monserrat, Lorenzo L
Publication Date: 2021-06-14

Variant appearance in text: TNNT2: Val85Leu
PubMed Link: 34127679
Variant Present in the following documents:
  • 41525_2021_204_MOESM1_ESM.pdf
View BVdb publication page



Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.

Clinical Cardiology
Fujino, Noboru N; Konno, Tetsuo T; Hayashi, Kenshi K; Hodatsu, Akihiko A; Fujita, Takashi T; Tsuda, Toyonobu T; Nagata, Yoji Y; Kawashiri, Masa-aki MA; Ino, Hidekazu H; Yamagishi, Masakazu M
Publication Date: 2013-03

Variant appearance in text: TNNT2: Val85Leu
PubMed Link: 23197398
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of QT variables on clinical outcome of genotyped hypertrophic cardiomyopathy.

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc
Uchiyama, Katsuharu K; Hayashi, Kenshi K; Fujino, Noboru N; Konno, Tetsuo T; Sakamoto, Yuichiro Y; Sakata, Kenji K; Kawashiri, Masa-aki MA; Ino, Hidekazu H; Yamagishi, Masakazu M
Publication Date: 2009-01

Variant appearance in text: TNNT2: Val85Leu
PubMed Link: 19149795
Variant Present in the following documents:
  • Main text
View BVdb publication page