Variant #0000002533 (NC_000002.12:g.1456232G>T, NM_000547.5:c.769G>T (TPO))
Individual ID |
00000549 |
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.1456232G>T |
Published as |
- |
Reference |
Ching Chin Lee et al.(2013) |
DB-ID |
TPO_000006 |
dbSNP ID |
rs4927611 |
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 |
2021-03-29 14:25:06 +08:00 (CST) |
Date last edited |
2021-08-01 13:34:37 +08:00 (CST) |

Variant on transcripts
Screenings
|
|