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NSF c.1126C>G ;(p.P376A)
Variant ID: 17-44771227-C-G
NM_006178.3(
NSF
):c.1126C>G;(p.P376A)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Characterizing microRNA editing and mutation sites in Autism Spectrum Disorder.
Frontiers In Molecular Neuroscience
Wu, Xingwang X; Yang, Huaide H; Lin, Han H; Suo, Angbaji A; Wu, Shuai S; Xie, Wenping W; Zhou, Nan N; Guo, Shiyong S; Ding, Hao H; Zhou, Guangchen G; Qiu, Zhichao Z; Shi, Hong H; Yang, Jun J; Zheng, Yun Y
Publication Date: 2022
Variant appearance in text: NSF: p376a
PubMed Link:
36743290
Variant Present in the following documents:
Main text
fnmol-15-1105278.pdf
View BVdb publication page
Endosomal system genetics and autism spectrum disorders: A literature review.
Neuroscience And Biobehavioral Reviews
Patak, Jameson J; Zhang-James, Yanli Y; Faraone, Stephen V SV
Publication Date: 2016-06
Variant appearance in text: NSF: 1126C>G
PubMed Link:
27048963
Variant Present in the following documents:
Main text
View BVdb publication page