Variant #0000002941 (NC_000007.14:g.208920T>C, NM_001348946.2:c.3435T>C (ABCB1))
Individual ID |
00000715 |
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.208920T>C |
Published as |
- |
Reference |
Zalina Zahari et al.(2018) |
DB-ID |
ABCB1_000007 |
dbSNP ID |
rs1045642 |
Frequency |
43.4% |
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 |
2021-06-27 15:40:40 +08:00 (CST) |
Date last edited |
2021-08-01 13:12:21 +08:00 (CST) |

Variant on transcripts
Screenings
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