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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