TTN c.66940G>T ;(p.D22314Y)

Variant ID: 2-179445166-C-A

NM_001267550.1(TTN):c.66940G>T;(p.D22314Y)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria.

American Journal Of Human Genetics
Pejaver, Vikas V; Byrne, Alicia B AB; Feng, Bing-Jian BJ; Pagel, Kymberleigh A KA; Mooney, Sean D SD; Karchin, Rachel R; O'Donnell-Luria, Anne A; Harrison, Steven M SM; Tavtigian, Sean V SV; Greenblatt, Marc S MS; Biesecker, Leslie G LG; Radivojac, Predrag P; Brenner, Steven E SE; ,
Publication Date: 2022-12-01

Variant appearance in text: N/A
PubMed Link: 36413997
Variant Present in the following documents:
View BVdb publication page



Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing.

Plos One
Kostareva, Anna A; Kiselev, Artem A; Gudkova, Alexandra A; Frishman, Goar G; Ruepp, Andreas A; Frishman, Dmitrij D; Smolina, Natalia N; Tarnovskaya, Svetlana S; Nilsson, Daniel D; Zlotina, Anna A; Khodyuchenko, Tatiana T; Vershinina, Tatiana T; Pervunina, Tatiana T; Klyushina, Alexandra A; Kozlenok, Andrey A; Sjoberg, Gunnar G; Golovljova, Irina I; Sejersen, Thomas T; Shlyakhto, Eugeniy E
Publication Date: 2016

Variant appearance in text: TTN: D22314Y
PubMed Link: 27662471
Variant Present in the following documents:
  • Main text
  • pone.0163362.pdf
View BVdb publication page