Variant #0000497199 (NC_000004.11:g.89039438A>G, NC_000004.11(NM_004827.2):c.690-26T>C (ABCG2))
Chromosome |
4 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89039438A>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
ABCG2_000086 |
Frequency |
1/13006 |
Freq. EA |
0/8600 |
Freq. AA |
1/4406 |
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 08:59:36 +02:00 (CEST) |

Variant on transcripts
|
|