Variant #0000001086 (NC_000002.12:g.21021128G>T, NC_000002.12(NM_000384.2):c.2817-1223C>A (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.21021128G>T |
Published as |
- |
Reference |
Livy Alex et al. (2012), dbSNP |
DB-ID |
APOB_000027 |
dbSNP ID |
rs10199768 |
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 10:05:49 +08:00 (CST) |
Date last edited |
2021-08-23 11:30:54 +08:00 (CST) |

Variant on transcripts
Screenings
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