Variant #0000008668 (NC_000017.11:g.43099914G>A, NC_000017.11(NM_007294.3):c.442-34C>T (BRCA1))
Individual ID |
00001532 |
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.43099914G>A |
Reference |
- |
DB-ID |
BRCA1_000012 See all 149 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Dolores Mansilla-Instituto Roffo |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-08 16:54:22 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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