Variant #0001888902 (NC_000021.8:g.43767776C>A, NC_000021.8(NM_005423.4):c.230-35G>T (TFF2))
| Chromosome |
21 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43767776C>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
TFF2_000015 |
| Frequency |
82/13006 |
| Freq. EA |
76/8600 |
| Freq. AA |
6/4406 |
| 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 16:49:50 +02:00 (CEST) |
| Date last edited |
2013-05-06 06:33:22 +02:00 (CEST) |

Variant on transcripts
|
|