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TRIM33 c.526+464G>T
Variant ID: 1-115052708-C-A
NM_015906.3(
TRIM33
):c.526+464G>T
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Novel functional variants at the GWAS-implicated loci might confer risk to major depressive disorder, bipolar affective disorder and schizophrenia.
Bmc Neuroscience
Bryzgalov, Leonid O LO; Korbolina, Elena E EE; Brusentsov, Ilja I II; Leberfarb, Elena Y EY; Bondar, Natalia P NP; Merkulova, Tatiana I TI
Publication Date: 2018-04-19
Variant appearance in text: rs3827735
PubMed Link:
29745862
Variant Present in the following documents:
Main text
12868_2018_Article_414.pdf
View BVdb publication page
A Comprehensive Atlas of E3 Ubiquitin Ligase Mutations in Neurological Disorders.
Frontiers In Genetics
George, Arlene J AJ; Hoffiz, Yarely C YC; Charles, Antoinette J AJ; Zhu, Ying Y; Mabb, Angela M AM
Publication Date: 2018
Variant appearance in text: rs3827735
PubMed Link:
29491882
Variant Present in the following documents:
Table1.xlsx, sheet 1
View BVdb publication page
Identification of long non-coding RNAs involved in neuronal development and intellectual disability.
Scientific Reports
D'haene, Eva E; Jacobs, Eva Z EZ; Volders, Pieter-Jan PJ; De Meyer, Tim T; Menten, Björn B; Vergult, Sarah S
Publication Date: 2016-06-20
Variant appearance in text: rs3827735
PubMed Link:
27319317
Variant Present in the following documents:
srep28396-s1.pdf
View BVdb publication page