Variant #0006099896 (NC_000009.11:g.99413924A>G, NC_000009.11(NM_153698.1):c.315+17T>C (AAED1))
| Chromosome |
9 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99413924A>G |
| DB-ID |
- |
| dbSNP ID |
rs28377520 |
| gnomAD frequency |
9073/242706 |
| gnomAD homozygote count |
2065/114345 |
| 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
|
|