TTN c.30587T>C ;(p.V10196A)

Variant ID: 2-179566266-A-G

NM_001267550.1(TTN):c.30587T>C;(p.V10196A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Integrative analysis reveals clinically relevant molecular fingerprints in pancreatic cancer.

Molecular Therapy. Nucleic Acids
Song, Libin L; Qi, Simin S; Hu, Wei W; Fang, Zhixiao Z; Yu, Dehua D; Liu, Teng T; Wu, Jingni J; Wu, Yangjun Y; Wu, Aiwei A; Feng, Lanyun L; Xie, Jing J; Zhang, Bo B; He, Wenguang W; Ning, Zhouyu Z; Liu, Luming L; Qin, Jiang-Jiang JJ; Li, Shengli S
Publication Date: 2021-12-03

Variant appearance in text: TTN: 30587T>C; V10196A
PubMed Link: 34513290
Variant Present in the following documents:
  • mmc3.xlsx, sheet 1
View BVdb publication page



The genetic landscape of benign thyroid nodules revealed by whole exome and transcriptome sequencing.

Nature Communications
Ye, Lei L; Zhou, Xiaoyi X; Huang, Fengjiao F; Wang, Weixi W; Qi, Yicheng Y; Xu, Heng H; Yang, Shu S; Shen, Liyun L; Fei, Xiaochun X; Xie, Jing J; Cao, Min M; Zhou, Yulin Y; Zhu, Wei W; Wang, Shu S; Ning, Guang G; Wang, Weiqing W
Publication Date: 2017-06-05

Variant appearance in text: TTN: V10196A
PubMed Link: 28580939
Variant Present in the following documents:
  • ncomms15533-s4.xlsx, sheet 1
View BVdb publication page