Variant #0000001137 (NC_000023.11:g.139548386G>A, NM_000133.3:c.415G>A (F9))
Individual ID |
00000227 |
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.139548386G>A |
Published as |
c.415G/A |
Reference |
- |
DB-ID |
F9_000010 See all 3 reported entries |
dbSNP ID |
rs398123393 |
Frequency |
1/10 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-12-07 11:46:15 +08:00 (CST) |
Date last edited |
2021-09-13 12:45:21 +08:00 (CST) |

Variant on transcripts
Screenings
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