Variant #0001900123 (NC_000022.10:g.17072145C>T, NM_014406.4:c.1296G>A (CCT8L2))
Chromosome |
22 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17072145C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
CCT8L2_000019 |
Frequency |
2/13006 |
Freq. EA |
2/8600 |
Freq. AA |
0/4406 |
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 |
2014-05-11 02:26:31 +02:00 (CEST) |

Variant on transcripts
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