DDX10 c.138G>C ;(p.W46C)

Variant ID: 11-108536018-G-C

NM_004398.2(DDX10):c.138G>C;(p.W46C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia.

Nature Communications
Yang, Minjun M; Vesterlund, Mattias M; Siavelis, Ioannis I; Moura-Castro, Larissa H LH; Castor, Anders A; Fioretos, Thoas T; Jafari, Rozbeh R; Lilljebjörn, Henrik H; Odom, Duncan T DT; Olsson, Linda L; Ravi, Naveen N; Woodward, Eleanor L EL; Harewood, Louise L; Lehtiö, Janne J; Paulsson, Kajsa K
Publication Date: 2019-04-03

Variant appearance in text: DDX10: W46C
PubMed Link: 30944321
Variant Present in the following documents:
  • 41467_2019_9469_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page