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SNCA c.-25-469G>A
Variant ID: 4-90757312-C-T
NM_000345.3(
SNCA
):c.-25-469G>A
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:
Frequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newborn.
Respiratory Research
Wang, Mingbang M; Zhuang, Deyi D; Mei, Mei M; Ma, Haiyan H; Li, Zixiu Z; He, Fusheng F; Cheng, Guoqiang G; Lin, Guang G; Zhou, Wenhao W
Publication Date: 2020-02-13
Variant appearance in text: rs2870027
PubMed Link:
32054482
Variant Present in the following documents:
12931_2020_1314_MOESM1_ESM.xlsx, sheet 7
View BVdb publication page
The Landscape of SNCA Transcripts Across Synucleinopathies: New Insights From Long Reads Sequencing Analysis.
Frontiers In Genetics
Tseng, Elizabeth E; Rowell, William J WJ; Glenn, Omolara-Chinue OC; Hon, Ting T; Barrera, Julio J; Kujawa, Steve S; Chiba-Falek, Ornit O
Publication Date: 2019
Variant appearance in text: rs2870027
PubMed Link:
31338105
Variant Present in the following documents:
Main text
fgene-10-00584.pdf
View BVdb publication page