Variant #0000002955 (NC_000019.10:g.4536T>C, NM_000660.7:c.-1347T>C (TGFB1))
Individual ID |
00000724 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.4536T>C |
Published as |
- |
Reference |
Azadeh Emami et al.(2012) |
DB-ID |
TGFB1_000002 |
dbSNP ID |
rs1800469 |
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 |
2021-06-28 12:33:10 +08:00 (CST) |
Date last edited |
2021-08-01 13:14:27 +08:00 (CST) |

Variant on transcripts
Screenings
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