Variant #0009873352 (NC_000016.9:g.48265826T>C, NM_032583.3:c.7A>G (ABCC11))
| Chromosome |
16 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.48265826T>C |
| DB-ID |
- |
| dbSNP ID |
rs200128517 |
| gnomAD frequency |
165/246230 |
| gnomAD homozygote count |
0/122950 |
| 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
|
|