DNAH11 c.4888T>C ;(p.F1630L)

Variant ID: 7-21678627-T-C

NM_001277115.1(DNAH11):c.4888T>C;(p.F1630L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular Analysis of Clinically Defined Subsets of High-Grade Serous Ovarian Cancer.

Cell Reports
Lee, Sanghoon S; Zhao, Li L; Rojas, Christine C; Bateman, Nicholas W NW; Yao, Hui H; Lara, Olivia D OD; Celestino, Joseph J; Morgan, Margaret B MB; Nguyen, Tri V TV; Conrads, Kelly A KA; Rangel, Kelly M KM; Dood, Robert L RL; Hajek, Richard A RA; Fawcett, Gloria L GL; Chu, Randy A RA; Wilson, Katlin K; Loffredo, Jeremy L JL; Viollet, Coralie C; Jazaeri, Amir A AA; Dalgard, Clifton L CL; Mao, Xizeng X; Song, Xingzhi X; Zhou, Ming M; Hood, Brian L BL; Banskota, Nirad N; Wilkerson, Matthew D MD; Te, Jerez J; Soltis, Anthony R AR; Roman, Kristin K; Dunn, Andrew A; Cordover, David D; Eterovic, Agda Karina AK; Liu, Jinsong J; Burks, Jared K JK; Baggerly, Keith A KA; Fleming, Nicole D ND; Lu, Karen H KH; Westin, Shannon N SN; Coleman, Robert L RL; Mills, Gordon B GB; Casablanca, Yovanni Y; Zhang, Jianhua J; Conrads, Thomas P TP; Maxwell, George L GL; Futreal, P Andrew PA; Sood, Anil K AK
Publication Date: 2020-04-14

Variant appearance in text: DNAH11: F1630L
PubMed Link: 32294438
Variant Present in the following documents:
  • NIHMS1584940-supplement-3.xlsx, sheet 1
View BVdb publication page