Variant #0000000908 (NC_000023.11:g.139530803delC, NM_000133.3:c.39delC (F9))
Individual ID |
00000176 |
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.139530803delC |
Published as |
L14Sfs*7 |
Reference |
Maimiza Zahari et al. (2018) |
DB-ID |
F9_000014 |
dbSNP ID |
- |
Frequency |
1/2 |
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 |
2020-11-24 12:48:21 +08:00 (CST) |
Date last edited |
2020-12-14 16:31:41 +08:00 (CST) |

Variant on transcripts
Screenings
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