Variant #0000003756 (NC_000004.11:g.90749305C>T, SNCA(NM_000345.3):c.152G>A)
| Individual ID |
00003756 |
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.90749305C>T |
| Reference |
Lesage S1, Anheim M, Letournel F, Bousset L, Honoré A, Rozas N, Pieri L, Madiona K, Dürr A, Melki R, Verny C, Brice A; French Parkinson's Disease Genetics Study Group.(2013) |
| DB-ID |
SNCA_000005 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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