Variant #0001900098 (NC_000022.10:g.16449632C>A, NM_001005239.1:c.173G>T (OR11H1))
| Chromosome |
22 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16449632C>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
OR11H1_000014 |
| Frequency |
1/9322 |
| Freq. EA |
0/6320 |
| Freq. AA |
1/3002 |
| 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 |
2016-10-09 15:51:50 +02:00 (CEST) |

Variant on transcripts
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