TTN c.69422_69426delinsAAAAGGACCC ;(p.G23141Efs*38)

Variant ID: 2-179441545-AGGGC-GGGTCCTTTT

NM_001267550.1(TTN):c.69422_69426delinsAAAAGGACCC;(p.G23141Efs*38)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.

Journal Of The American Heart Association
Ramchand, Jay J; Wallis, Mathew M; Macciocca, Ivan I; Lynch, Elly E; Farouque, Omar O; Martyn, Melissa M; Phelan, Dean D; Chong, Belinda B; Lockwood, Siobhan S; Weintraub, Robert R; Thompson, Tina T; Trainer, Alison A; Zentner, Dominica D; Vohra, Jitendra J; Chetrit, Michael M; Hare, David L DL; James, Paul P
Publication Date: 2020-01-21

Variant appearance in text: TTN: 69422_69426delinsAAAAGGACCC; Gly23141Glufs*38
PubMed Link: 31931689
Variant Present in the following documents:
  • Main text
  • JAH3-9-e013346.pdf
View BVdb publication page