DDX10 c.877A>G ;(p.I293V)

Variant ID: 11-108559691-A-G

NM_004398.2(DDX10):c.877A>G;(p.I293V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Identification of NCAN as a candidate gene for developmental dyslexia.

Scientific Reports
Einarsdottir, Elisabet E; Peyrard-Janvid, Myriam M; Darki, Fahimeh F; Tuulari, Jetro J JJ; Merisaari, Harri H; Karlsson, Linnea L; Scheinin, Noora M NM; Saunavaara, Jani J; Parkkola, Riitta R; Kantojärvi, Katri K; Ämmälä, Antti-Jussi AJ; Yiu-Lin Yu, Nancy N; Matsson, Hans H; Nopola-Hemmi, Jaana J; Karlsson, Hasse H; Paunio, Tiina T; Klingberg, Torkel T; Leinonen, Eira E; Kere, Juha J
Publication Date: 2017-08-24

Variant appearance in text: DDX10: I293V
PubMed Link: 28839234
Variant Present in the following documents:
  • 41598_2017_10175_MOESM4_ESM.xls, sheet 1
View BVdb publication page