Variant #0000001029 (NC_000002.12:g.21002881C>T, NM_000384.2:c.12541G>A (APOB))
Individual ID |
00000201 |
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.21002881C>T |
Published as |
- |
Reference |
ClinVar |
DB-ID |
APOB_000017 |
dbSNP ID |
- |
Frequency |
1/9 |
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 |
2020-11-30 12:55:28 +08:00 (CST) |
Date last edited |
2020-12-14 17:09:20 +08:00 (CST) |

Variant on transcripts
Screenings
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