DNAH11 c.11096A>C ;(p.N3699T)

Variant ID: 7-21893967-A-C

NM_001277115.1(DNAH11):c.11096A>C;(p.N3699T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Integrated exome and RNA sequencing of TFE3-translocation renal cell carcinoma.

Nature Communications
Sun, Guangxi G; Chen, Junru J; Liang, Jiayu J; Yin, Xiaoxue X; Zhang, Mengni M; Yao, Jin J; He, Ning N; Armstrong, Cameron M CM; Zheng, Linmao L; Zhang, Xingming X; Zhu, Sha S; Sun, Xiaomeng X; Yang, Xiaoxia X; Zhao, Wanbin W; Liao, Banghua B; Pan, Xiuyi X; Nie, Ling L; Yang, Ling L; Chen, Yuntian Y; Zhao, Jinge J; Zhang, Haoran H; Dai, Jindong J; Shen, Yali Y; Liu, Jiyan J; Huang, Rui R; Liu, Jiandong J; Wang, Zhipeng Z; Ni, Yuchao Y; Wei, Qiang Q; Li, Xiang X; Zhou, Qiao Q; Huang, Haojie H; Liu, Zhenhua Z; Shen, Pengfei P; Chen, Ni N; Zeng, Hao H
Publication Date: 2021-09-06

Variant appearance in text: DNAH11: 11096A>C; N3699T
PubMed Link: 34489456
Variant Present in the following documents:
  • 41467_2021_25618_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page