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CUX1 c.1741C>T ;(p.L581=)
Variant ID: 7-101840432-C-T
NM_181552.3(
CUX1
):c.1741C>T;(p.L581=)
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:
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Ebiomedicine
Wang, Tao T; Zhao, Tingting T; Liu, Liqiu L; Teng, Huajing H; Fan, Tianda T; Li, Yi Y; Wang, Yan Y; Li, Jinchen J; Xia, Kun K; Sun, Zhongsheng Z
Publication Date: 2022-07
Variant appearance in text: CUX1: 1741C>T; P581S
PubMed Link:
35665681
Variant Present in the following documents:
mmc26.xlsx, sheet 1
View BVdb publication page