DNAH11 c.1072_1074delinsTGG ;(p.R358W)

Variant ID: 7-21603893-CGC-TGG

NM_001277115.1(DNAH11):c.1072_1074delinsTGG;(p.R358W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification and ranking of recurrent neo-epitopes in cancer.

Bmc Medical Genomics
Blanc, Eric E; Holtgrewe, Manuel M; Dhamodaran, Arunraj A; Messerschmidt, Clemens C; Willimsky, Gerald G; Blankenstein, Thomas T; Beule, Dieter D
Publication Date: 2019-11-27

Variant appearance in text: DNAH11: R358W
PubMed Link: 31775766
Variant Present in the following documents:
  • 12920_2019_611_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page