DNAH11 c.877G>T ;(p.D293Y)

Variant ID: 7-21599405-G-T

NM_001277115.1(DNAH11):c.877G>T;(p.D293Y)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Multi-region exome sequencing reveals the intratumoral heterogeneity of surgically resected small cell lung cancer.

Nature Communications
Zhou, Huaqiang H; Hu, Yi Y; Luo, Rongzhen R; Zhao, Yuanyuan Y; Pan, Hui H; Ji, Liyan L; Zhou, Ting T; Zhang, Lanjun L; Long, Hao H; Fu, Jianhua J; Wen, Zhesheng Z; Wang, Siyu S; Wang, Xin X; Lin, Peng P; Yang, Haoxian H; Wang, Junye J; Song, Mengmeng M; Yi, Xin X; Yang, Ling L; Xia, Xuefang X; Guan, Yanfang Y; Fang, Wenfeng W; Yang, Yunpeng Y; Hong, Shaodong S; Huang, Yan Y; Li, Pansong P; Zhang, Yaxiong Y; Zhou, Ningning N
Publication Date: 2021-09-14

Variant appearance in text: DNAH11: 877G>T; D293Y
PubMed Link: 34521849
Variant Present in the following documents:
  • 41467_2021_25787_MOESM4_ESM.xlsx, sheet 1
  • 41467_2021_25787_MOESM10_ESM.xlsx, sheet 7
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NOTCH target gene HES5 mediates oncogenic and tumor suppressive functions in hepatocarcinogenesis.

Oncogene
Luiken, Sarah S; Fraas, Angelika A; Bieg, Matthias M; Sugiyanto, Raisatun R; Goeppert, Benjamin B; Singer, Stephan S; Ploeger, Carolin C; Warsow, Gregor G; Marquardt, Jens U JU; Sticht, Carsten C; De La Torre, Carolina C; Pusch, Stefan S; Mehrabi, Arianeb A; Gretz, Norbert N; Schlesner, Matthias M; Eils, Roland R; Schirmacher, Peter P; Longerich, Thomas T; Roessler, Stephanie S
Publication Date: 2020-04

Variant appearance in text: DNAH11: 877G>T; D293Y
PubMed Link: 32055024
Variant Present in the following documents:
  • 41388_2020_1198_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Combined immunodeficiency in a patient with c-Rel deficiency.

The Journal Of Allergy And Clinical Immunology
Beaussant-Cohen, Sarah S; Jaber, Faris F; Massaad, Michel J MJ; Weeks, Sabrina S; Jones, Jennifer J; Alosaimi, Mohammed F MF; Wallace, Jacqueline J; Al-Herz, Waleed W; Geha, Raif S RS; Chou, Janet J
Publication Date: 2019-08

Variant appearance in text: DNAH11: 877G>T
PubMed Link: 31103457
Variant Present in the following documents:
  • Main text
View BVdb publication page