Variant #0001427321 (NC_000015.9:g.89736558T>C, NC_000015.9(NM_007011.7):c.1081+8T>C (ABHD2))
| Chromosome |
15 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89736558T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABHD2_000067 |
| Frequency |
5112/12998 |
| Freq. EA |
3525/8598 |
| Freq. AA |
1587/4400 |
| 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 16:41:46 +02:00 (CEST) |
| Date last edited |
2018-08-23 09:25:10 +02:00 (CEST) |

Variant on transcripts
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