Variant #0000226969 (NC_000002.11:g.44080053C>T, NC_000002.11(NM_022437.2):c.964+46C>T (ABCG8))
| Chromosome |
2 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44080053C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCG8_000092 |
| Frequency |
87/12952 |
| Freq. EA |
1/8566 |
| Freq. AA |
86/4386 |
| 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 |
2018-08-22 23:50:09 +02:00 (CEST) |

Variant on transcripts
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