Variant #0000497165 (NC_000004.11:g.89028478T>A, NC_000004.11(NM_004827.2):c.1195-60A>T (ABCG2))
| Chromosome |
4 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89028478T>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCG2_000052 |
| Frequency |
1266/4562 |
| Freq. EA |
1165/3178 |
| Freq. AA |
101/1384 |
| 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 |
2018-08-23 07:26:46 +02:00 (CEST) |

Variant on transcripts
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