TTN c.78119T>C ;(p.V26040A)

Variant ID: 2-179432740-A-G

NM_001267550.1(TTN):c.78119T>C;(p.V26040A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.

Journal Of Personalized Medicine
Martínez-Barrios, Estefanía E; Sarquella-Brugada, Georgia G; Pérez-Serra, Alexandra A; Fernández-Falgueras, Anna A; Cesar, Sergi S; Coll, Mónica M; Puigmulé, Marta M; Iglesias, Anna A; Alcalde, Mireia M; Vallverdú-Prats, Marta M; Ferrer-Costa, Carles C; Del Olmo, Bernat B; Picó, Ferran F; López, Laura L; Fiol, Victoria V; Cruzalegui, José J; Hernández, Clara C; Arbelo, Elena E; Grassi, Simone S; Oliva, Antonio A; Toro, Rocío R; Brugada, Josep J; Brugada, Ramon R; Campuzano, Oscar O
Publication Date: 2022-02-08

Variant appearance in text: TTN: 78119T>C
PubMed Link: 35207729
Variant Present in the following documents:
  • jpm-12-00241.pdf
View BVdb publication page