Variant #0000008974 (NC_000013.11:g.32333105C>T, NM_000059.3:c.1627C>T (BRCA2))
Individual ID |
00001657 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32333105C>T |
Reference |
- |
DB-ID |
BRCA2_000218 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Silvina Sisterna-Hospital de Comunidad |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2021-08-02 23:46:18 -03:00 (-03) |
Date last edited |
2021-10-06 15:32:19 -03:00 (-03) |
Variant on transcripts
Screenings
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