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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