Variant #0000006855 (NC_000017.11:g.43082453A>G, NM_007294.3:c.4308T>C (BRCA1))
Individual ID |
00001172 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.43082453A>G |
Reference |
- |
DB-ID |
BRCA1_000008 See all 287 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-06-01 17:01:05 -03:00 (-03) |
Date last edited |
N/A |
![Options](gfx/options_button.png)
Variant on transcripts
Screenings
|
|