Variant #0000007636 (NC_000013.11:g.32338918A>G, NM_000059.3:c.4563A>G (BRCA2))
Individual ID |
00001298 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32338918A>G |
Reference |
- |
DB-ID |
BRCA2_000010 See all 169 reported entries |
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 |
2020-07-31 12:59:58 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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