Variant #0000002209 (NC_000013.11:g.32398370T>A, NM_000059.3:c.9857T>A (BRCA2))
Individual ID |
00000426 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32398370T>A |
Published as |
- |
Reference |
Wei Xiong Wen et al. (2018), dbSNP, ClinVar |
DB-ID |
BRCA2_000163 |
dbSNP ID |
rs398122624 |
Frequency |
1/490 |
Variant remarks |
VUS (variants of unknown significance) |
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 |
2021-02-25 15:48:50 +08:00 (CST) |
Date last edited |
2021-08-01 12:53:47 +08:00 (CST) |

Variant on transcripts
Screenings
|
|