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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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