Variant #0000002095 (NC_000004.12:g.9961141T>C, NC_000004.12(NM_001001290.1):c.595-19096A>G (SLC2A9))
Individual ID |
00000447 |
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.9961141T>C |
Published as |
- |
Reference |
dbSNP |
DB-ID |
SLC2A9_000003 |
dbSNP ID |
rs11942223 |
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 11:18:35 +08:00 (CST) |
Date last edited |
2021-08-01 13:04:07 +08:00 (CST) |

Variant on transcripts
Screenings
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