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NCAN c.3115G>T ;(p.A1039S)
Variant ID: 19-19344693-G-T
NM_004386.2(
NCAN
):c.3115G>T;(p.A1039S)
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: rs146011974
PubMed Link:
28839234
Variant Present in the following documents:
41598_2017_10175_MOESM1_ESM.pdf
View BVdb publication page