DNAH11 c.1765_1766delinsCC ;(p.S589P)

Variant ID: 7-21627736-AG-CC

NM_001277115.1(DNAH11):c.1765_1766delinsCC;(p.S589P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Joint mouse-human phenome-wide association to test gene function and disease risk.

Nature Communications
Wang, Xusheng X; Pandey, Ashutosh K AK; Mulligan, Megan K MK; Williams, Evan G EG; Mozhui, Khyobeni K; Li, Zhengsheng Z; Jovaisaite, Virginija V; Quarles, L Darryl LD; Xiao, Zhousheng Z; Huang, Jinsong J; Capra, John A JA; Chen, Zugen Z; Taylor, William L WL; Bastarache, Lisa L; Niu, Xinnan X; Pollard, Katherine S KS; Ciobanu, Daniel C DC; Reznik, Alexander O AO; Tishkov, Artem V AV; Zhulin, Igor B IB; Peng, Junmin J; Nelson, Stanley F SF; Denny, Joshua C JC; Auwerx, Johan J; Lu, Lu L; Williams, Robert W RW
Publication Date: 2016-02-02

Variant appearance in text: Dnahc11: S589P
PubMed Link: 26833085
Variant Present in the following documents:
  • ncomms10464-s5.xlsx, sheet 1
View BVdb publication page