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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