Variant #0000003813 (NC_000004.11:g.90749307A>T, SNCA(NM_000345.3):c.150T>A)
Individual ID |
00003813 |
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.90749307A>T |
Reference |
Khalaf O1, Fauvet B1, Oueslati A1, Dikiy I2, Mahul-Mellier AL1, Ruggeri FS3, Mbefo MK1, Vercruysse F1, Dietler G3, Lee SJ4, Eliezer D2, Lashuel HA5.(2014) |
DB-ID |
SNCA_000006 See all 6 reported entries |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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