Variant #0000002606 (NC_000006.12:g.7231C>T, NM_000500.9:c.1069C>T (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.7231C>T |
Published as |
p.R356W |
Reference |
P Balraj et al.(2013) |
DB-ID |
CYP21A2_000001 |
dbSNP ID |
rs7769409 |
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 10:52:32 +08:00 (CST) |
Date last edited |
2021-08-01 14:09:54 +08:00 (CST) |

Variant on transcripts
Screenings
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