Variant #0007486008 (NC_000011.9:g.77531791del, NM_016578.3:c.-31delC (RSF1))
| Chromosome |
11 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.77531791del |
| DB-ID |
- |
| dbSNP ID |
rs774876677 |
| gnomAD frequency |
3/122838 |
| gnomAD homozygote count |
1/61414 |
| 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
|
|