Variant #0000001134 (NC_000023.11:g.139562070A>G, NM_000133.3:c.1385A>G (F9))
Individual ID |
00000227 |
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.139562070A>G |
Published as |
c. 1385A/G |
Reference |
dbSNP, ClinVar |
DB-ID |
F9_000018 |
dbSNP ID |
rs561793582 |
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 11:34:40 +08:00 (CST) |
Date last edited |
2021-08-23 16:03:29 +08:00 (CST) |

Variant on transcripts
Screenings
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