Variant #0000960915 (NC_000009.11:g.139916485_139916486insG, NC_000009.11(NM_001606.4):c.568-33_568-32insC (ABCA2))
| Chromosome |
9 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.139916485_139916486insG |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCA2_000485 |
| Frequency |
2702/10822 |
| Freq. EA |
1939/7390 |
| Freq. AA |
763/3432 |
| Average frequency (gnomAD v.2.1.1) |
- |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Ivo F.A.C. Fokkema |
| Date created |
2013-05-03 16:29:58 +02:00 (CEST) |
| Date last edited |
2018-08-23 09:11:03 +02:00 (CEST) |

Variant on transcripts
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