Variant #0000001082 (NC_000002.12:g.21015541C>G, NM_000384.2:c.3337G>C (APOB))
Individual ID |
00000214 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.21015541C>G |
Published as |
- |
Reference |
Livy Alex et al. (2012), dbSNP |
DB-ID |
APOB_000023 |
dbSNP ID |
rs12713844 |
Frequency |
1/17 |
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 |
2020-12-03 09:57:31 +08:00 (CST) |
Date last edited |
2021-08-23 11:26:37 +08:00 (CST) |

Variant on transcripts
Screenings
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