Variant #0000002367 (NC_000013.11:g.32337954_32337955del, NM_000059.3:c.3599_3600del (BRCA2))
Individual ID |
00000512 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32337954_32337955del |
Published as |
- |
Reference |
Timothy R Rebbeck et al.(2018) |
DB-ID |
BRCA2_000103 |
dbSNP ID |
rs80359391 |
Frequency |
1/64 families |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nur Aisyah Athirah |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nur Aisyah Athirah |
Date created |
2021-03-15 10:26:14 +08:00 (CST) |
Date last edited |
2021-08-01 12:31:35 +08:00 (CST) |

Variant on transcripts
Screenings
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