Variant #0000002655 (NC_000002.12:g.21002394T>C, NM_000384.2:c.13028A>G (APOB))
Individual ID |
00000595 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.21002394T>C |
Published as |
- |
Reference |
Alyaa R Al-Khateeb et al.(2013) |
DB-ID |
APOB_000035 |
dbSNP ID |
- |
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 |
2021-04-25 14:51:38 +08:00 (CST) |
Date last edited |
2021-08-01 14:13:24 +08:00 (CST) |

Variant on transcripts
Screenings
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