Variant #0000497226 (NC_000004.11:g.89053657_89053658insC, NC_000004.11(NM_004827.2):c.263+70_263+71insG (ABCG2))
| Chromosome |
4 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89053657_89053658insC |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCG2_000113 |
| Frequency |
34/12520 |
| Freq. EA |
4/8254 |
| Freq. AA |
30/4266 |
| 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 16:25:12 +02:00 (CEST) |
| Date last edited |
2025-01-02 20:53:51 +01:00 (CET) |

Variant on transcripts
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