Variant #0001234621 (NC_000012.11:g.100930396T>A, NC_000012.11(NM_005123.3):c.819+8T>A (NR1H4))
| Chromosome |
12 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.100930396T>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
NR1H4_000044 |
| Frequency |
108/12988 |
| Freq. EA |
88/8582 |
| Freq. AA |
20/4406 |
| 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 16:39:18 +02:00 (CEST) |
| Date last edited |
2013-05-05 03:59:29 +02:00 (CEST) |

Variant on transcripts
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