Variant #0000000621 (NC_000013.11:g.32370993G>A, NM_000059.3:c.8525G>A (BRCA2))
Individual ID |
00000109 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32370993G>A |
Published as |
- |
Reference |
P S Ng et al. (2016), dbSNP, ClinVar |
DB-ID |
BRCA2_000088 |
dbSNP ID |
rs80359105 |
Frequency |
1/8 |
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 16:02:55 +08:00 (CST) |
Date last edited |
2021-08-22 11:22:41 +08:00 (CST) |

Variant on transcripts
Screenings
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