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SNCA c.112C>A ;(p.L38I)
Variant ID: 4-90756707-G-T
NM_000345.3(
SNCA
):c.112C>A;(p.L38I)
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: L38I
PubMed Link:
26315598
Variant Present in the following documents:
Main text
emm201554a.pdf
View BVdb publication page