Variant #0000010046 (NC_000011.10:g.67490415G>A, NM_003977.3:c.745G>A (AIP))
Individual ID |
00002981 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.67490415G>A |
Reference |
- |
DB-ID |
AIP_000002 |
dbSNP ID |
rs1313811815 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Guillermo Alberto-Instituto Fleming |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2024-07-05 15:14:21 -03:00 (-03) |
Date last edited |
N/A |
![Options](gfx/options_button.png)
Variant on transcripts
Screenings
|
|