Variant #0000009460 (NC_000013.11:g.32326499G>T, NM_000059.3:c.517G>T (BRCA2))
Individual ID |
00002224 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32326499G>T |
Reference |
- |
DB-ID |
BRCA2_000109 See all 18 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 |
2023-04-14 16:02:14 -03:00 (-03) |
Date last edited |
2024-07-25 16:21:54 -03:00 (-03) |
Variant on transcripts
Screenings
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