TTN c.79276del ;(p.R26426Efs*9)

Variant ID: 2-179431582-CT-C

NM_001267550.1(TTN):c.79276del;(p.R26426Efs*9)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.

Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-09-06

Variant appearance in text: TTN: 79276delA
PubMed Link: 34486814
Variant Present in the following documents:
  • Main text
  • EHF2-8-5178.pdf
View BVdb publication page


Myocardial ultrastructure can augment genetic testing for sporadic dilated cardiomyopathy with initial heart failure.

Esc Heart Failure
Saito, Tsunenori T; Sato, Naoko Saito NS; Mozawa, Kosuke K; Adachi, Akiko A; Sasaki, Yoshihiro Y; Nakamura, Kotoka K; Oka, Eiichiro E; Otsuka, Toshiaki T; Kodani, Eitaro E; Asai, Kuniya K; Mizuno, Kyoichi K; Shimizu, Wataru W; Gottlieb, Roberta A RA
Publication Date: 2021-12

Variant appearance in text: TTN: 79276delA
PubMed Link: 34486814
Variant Present in the following documents:
  • Main text
  • EHF2-8-5178.pdf
View BVdb publication page