Variant #0000004493 (NC_000013.11:g.32325251A>C, NC_000013.11(NM_000059.3):c.425+67A>C (BRCA2))
Individual ID |
00000572 |
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.32325251A>C |
Reference |
- |
DB-ID |
BRCA2_000014 See all 25 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Laura Igarzabal-CEMIC |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2018-08-03 16:15:38 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
|
|