Variant #0000226901 (NC_000002.11:g.44071788G>A, NC_000002.11(NM_022437.2):c.165+41G>A (ABCG8))
Chromosome |
2 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44071788G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
ABCG8_000039 |
Frequency |
113/13006 |
Freq. EA |
103/8600 |
Freq. AA |
10/4406 |
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 16:22:05 +02:00 (CEST) |
Date last edited |
2018-08-23 10:33:11 +02:00 (CEST) |

Variant on transcripts
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