Variant #0000003069 (NC_000017.11:g.10485T>C, NM_000342.4:c.92T>C (SLC4A1))
Individual ID |
00000793 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.10485T>C |
Published as |
- |
Reference |
Keng E Choo et al.(2006) |
DB-ID |
SLC4A1_000004 |
dbSNP ID |
rs55773290 |
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 |
2021-07-19 10:09:44 +08:00 (CST) |
Date last edited |
2021-07-25 13:21:39 +08:00 (CST) |

Variant on transcripts
Screenings
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