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 +08:00 (CST) |
Date last edited |
2017-11-22 09:42:14 +08:00 (CST) |

Variant on transcripts
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