Variant #0000002640 (NC_000013.11:g.32332592A>C, NM_000059.3:c.1114A>C (BRCA2))
Individual ID |
00000591 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32332592A>C |
Published as |
- |
Reference |
Mohamed Saleem et al.(2018) |
DB-ID |
BRCA2_000138 |
dbSNP ID |
rs144848 |
Frequency |
- |
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 |
2021-04-21 10:29:49 +08:00 (CST) |
Date last edited |
2021-08-01 12:33:34 +08:00 (CST) |

Variant on transcripts
Screenings
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