Variant #0000989577 (NC_000010.10:g.52566611C>T, NM_014576.3:c.1639G>A (A1CF))
| Chromosome |
10 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52566611C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
A1CF_000014 |
| Frequency |
430/13006 |
| Freq. EA |
7/8600 |
| Freq. AA |
423/4406 |
| 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 16:30:47 +02:00 (CEST) |
| Date last edited |
2024-04-27 17:39:15 +02:00 (CEST) |

Variant on transcripts
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