Variant #0001900110 (NC_000022.10:g.17071894G>A, NM_014406.4:c.1547C>T (CCT8L2))
| Chromosome |
22 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17071894G>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CCT8L2_000006 |
| Frequency |
2/13002 |
| Freq. EA |
0/8596 |
| Freq. AA |
2/4406 |
| 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 16:50:05 +02:00 (CEST) |
| Date last edited |
2014-05-03 20:25:22 +02:00 (CEST) |

Variant on transcripts
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