Variant #0000200395 (NC_000002.11:g.45622G>T, NM_001077710.2:c.764C>A (FAM110C))
| Chromosome |
2 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45622G>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
FAM110C_000016 |
| Frequency |
1/12698 |
| Freq. EA |
1/8464 |
| Freq. AA |
0/4234 |
| 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 |
2014-04-28 05:35:48 +02:00 (CEST) |

Variant on transcripts
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