Variant #0000000099 (NC_000023.11:g.139567145C>T, NM_000133.3:c.*5074C>T (F9))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg38 / GRCh38) |
g.139567145C>T |
| Published as |
- |
| Reference |
Balraj P et al. (2012) |
| DB-ID |
F9_000002 |
| dbSNP ID |
- |
| Frequency |
16 |
| Variant remarks |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
MyHVP |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
MyHVP |
| Date created |
2017-11-21 17:43:23 +00:00 (UTC) |
| Date last edited |
2017-11-22 09:42:14 +00:00 (UTC) |

Variant on transcripts
|
|