TTN c.67348C>T ;(p.Q22450*)

Variant ID: 2-179444666-G-A

NM_001267550.1(TTN):c.67348C>T;(p.Q22450*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Decoding Somatic Driver Gene Mutations and Affected Signaling Pathways in Human Medulloblastoma Subgroups.

Journal Of Cancer
Robbins, Charles J CJ; Bou-Dargham, Mayassa J MJ; Sanchez, Kevin K; Rosen, Matthew C MC; Sang, Qing-Xiang Amy QA
Publication Date: 2018

Variant appearance in text: TTN: Q22450X
PubMed Link: 30588243
Variant Present in the following documents:
  • jcav09p4596s2.xlsx, sheet 1
View BVdb publication page



Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.

Journal Of Translational Medicine
Lu, Chaoxia C; Wu, Wei W; Liu, Fang F; Yang, Kunqi K; Li, Jiacheng J; Liu, Yaping Y; Wang, Rongrong R; Si, Nuo N; Gao, Peng P; Liu, Yongtai Y; Zhang, Shuyang S; Zhang, Xue X
Publication Date: 2018-08-30

Variant appearance in text: TTN: Q22450X
PubMed Link: 30165862
Variant Present in the following documents:
  • 12967_2018_1605_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page