Variant #0008378479 (NC_000012.11:g.125558499A>G, NM_023928.3:c.211A>G (AACS))
| Chromosome |
12 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.125558499A>G |
| DB-ID |
- |
| dbSNP ID |
rs762567525 |
| gnomAD frequency |
1/246202 |
| gnomAD homozygote count |
0/123100 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Database submission license |
No license selected |
| Created by |
LOVD |
| Date created |
2017-02-27 00:00:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|
|