Variant #0000000623 (NC_000013.11:g.32340437_32340441del5, NM_000059.3:c.6082_6086del5 (BRCA2))
Individual ID |
00000110 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32340437_32340441del5 |
Published as |
- |
Reference |
P S Ng et al. (2016), dbSNP, ClinVar |
DB-ID |
BRCA2_000089 |
dbSNP ID |
rs80359558 |
Frequency |
1 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Nuur Athirah Binti Mohd Daud |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Nuur Athirah Binti Mohd Daud |
Date created |
2020-11-01 16:12:30 +08:00 (CST) |
Date last edited |
2021-08-22 11:26:31 +08:00 (CST) |

Variant on transcripts
Screenings
|
|