Variant #0000000042 (NC_000013.10:g.32969071G>C, NC_000013.10(NM_000059.3):c.9501+1G>C (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32969071G>C |
Reference |
- |
DB-ID |
BRCA2_000013 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2018-12-07 11:21:44 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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