Variant #0000004726 (NC_000013.11:g.32399139A>C, BRCA2(NM_000059.3):c.*369A>C)
Individual ID |
00000598 |
Chromosome |
13 |
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.32399139A>C |
Reference |
- |
DB-ID |
BRCA2_000149 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Private Practice |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Variant on transcripts
Screenings
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