Variant #0000002608 (NC_000006.12:g.6122T>A, NM_000500.9:c.515T>A (CYP21A2))
Individual ID |
00000582 |
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.6122T>A |
Published as |
p.I172N |
Reference |
P Balraj et al.(2013) |
DB-ID |
CYP21A2_000003 |
dbSNP ID |
rs6475 |
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 |
2021-04-18 11:00:19 +08:00 (CST) |
Date last edited |
2021-08-01 14:09:55 +08:00 (CST) |

Variant on transcripts
Screenings
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