Variant #0000003026 (NC_000017.11:g.12139G>C, NM_000546.5:c.*7657470C>G (TP53))
Individual ID |
00000762 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.12139G>C |
Published as |
- |
Reference |
A R Ghani et al.(2008) |
DB-ID |
TP53_000060 |
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 |
2021-07-06 13:02:01 +08:00 (CST) |
Date last edited |
2021-08-01 13:21:44 +08:00 (CST) |

Variant on transcripts
Screenings
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