Variant #0000000250 (NC_000013.10:g.32913452T>G, NM_000059.3:c.4960T>G (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably does not affect function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32913452T>G |
Reference |
- |
DB-ID |
BRCA2_000033 |
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 |
2023-06-27 13:37:26 +00:00 (UTC) |
Date last edited |
2024-05-13 11:24:26 +00:00 (UTC) |
Variant on transcripts
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