Variant #0000000778 (NC_000022.11:g.42126746C>T, NM_000106.6:c.1322G>A (CYP2D6))
Individual ID |
00000151 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.42126746C>T |
Published as |
4045G>A |
Reference |
Fee Wai Chin et al. (2016), dbSNP |
DB-ID |
CYP2D6_000005 |
dbSNP ID |
rs532668079 |
Frequency |
1/7 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-11-17 10:49:01 +08:00 (CST) |
Date last edited |
2021-09-12 15:02:03 +08:00 (CST) |

Variant on transcripts
Screenings
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