SNCA c.125C>A ;(p.S42Y)

Variant ID: 4-90749332-G-T

NM_000345.3(SNCA):c.125C>A;(p.S42Y)

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:

Transcriptional mutagenesis by 8-oxodG in α-synuclein aggregation and the pathogenesis of Parkinson's disease.

Experimental & Molecular Medicine
Basu, Sambuddha S; Je, Goun G; Kim, Yoon-Seong YS
Publication Date: 2015-08-28

Variant appearance in text: SNCA: S42Y
PubMed Link: 26315598
Variant Present in the following documents:
  • Main text
  • emm201554a.pdf
View BVdb publication page