Variant #0010681092 (NC_000017.10:g.48761142C>T, NM_003786.3:c.3954+25delCinsT (ABCC3))
| Chromosome |
17 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48761142C>T |
| DB-ID |
- |
| dbSNP ID |
rs377011162 |
| gnomAD frequency |
6/225306 |
| gnomAD homozygote count |
0/112646 |
| 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
|
|