Variant #0000002094 (NC_000004.12:g.9939182G>A, NC_000004.12(NM_001001290.1):c.727+2731C>T (SLC2A9))
Individual ID |
00000447 |
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.9939182G>A |
Published as |
- |
Reference |
dbSNP |
DB-ID |
SLC2A9_000002 |
dbSNP ID |
rs5028843 |
Frequency |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nur Aisyah Athirah |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nur Aisyah Athirah |
Date created |
2021-02-22 11:17:22 +08:00 (CST) |
Date last edited |
2021-08-01 13:04:07 +08:00 (CST) |

Variant on transcripts
Screenings
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