Variant #0005390255 (NC_000008.10:g.116928C>G, NM_001005504.1:c.97G>C (OR4F21))
| Chromosome |
8 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.116928C>G |
| DB-ID |
- |
| dbSNP ID |
rs749479527 |
| gnomAD frequency |
2/31580 |
| gnomAD homozygote count |
1/15789 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Database submission license |
No license selected |
| Created by |
LOVD |
| Date created |
2017-02-27 00:00:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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