Variant #0001323965 (NC_000014.8:g.51371121C>T, NM_001206673.1:c.*37C>T (ABHD12B))
| Chromosome |
14 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.51371121C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABHD12B_000080 |
| Frequency |
2318/13006 |
| Freq. EA |
1643/8600 |
| Freq. AA |
675/4406 |
| 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 16:41:19 +02:00 (CEST) |
| Date last edited |
2018-08-23 01:26:35 +02:00 (CEST) |

Variant on transcripts
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