Variant #0009677600 (NC_000016.9:g.8829684T>G, NC_000016.9(NM_000663.4):c.70+18T>G (ABAT))
| Chromosome |
16 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8829684T>G |
| DB-ID |
- |
| dbSNP ID |
rs866966999 |
| gnomAD frequency |
1/201968 |
| gnomAD homozygote count |
0/100983 |
| 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
|
|