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.




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