TTN c.63898C>T ;(p.H21300Y)

Variant ID: 2-179452040-G-A

NM_001267550.1(TTN):c.63898C>T;(p.H21300Y)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetics of Cardiomyopathy: Clinical and Mechanistic Implications for Heart Failure.

Korean Circulation Journal
Kim, Kyung-Hee KH; Pereira, Naveen L NL
Publication Date: 2021-10

Variant appearance in text: TTN: 63898C>T
PubMed Link: 34327881
Variant Present in the following documents:
  • kcj-51-797.pdf
View BVdb publication page



Extreme intratumour heterogeneity and driver evolution in mismatch repair deficient gastro-oesophageal cancer.

Nature Communications
von Loga, Katharina K; Woolston, Andrew A; Punta, Marco M; Barber, Louise J LJ; Griffiths, Beatrice B; Semiannikova, Maria M; Spain, Georgia G; Challoner, Benjamin B; Fenwick, Kerry K; Simon, Ronald R; Marx, Andreas A; Sauter, Guido G; Lise, Stefano S; Matthews, Nik N; Gerlinger, Marco M
Publication Date: 2020-01-16

Variant appearance in text: TTN: H21300Y
PubMed Link: 31949146
Variant Present in the following documents:
  • 41467_2019_13915_MOESM4_ESM.xlsx, sheet 5
View BVdb publication page