Variant #0000009184 (NC_000013.11:g.32379413G>A, NM_000059.3:c.8851G>A (BRCA2))
Individual ID |
00001855 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32379413G>A |
Reference |
- |
DB-ID |
BRCA2_000058 See all 15 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2021-11-24 16:31:04 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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