Variant #0000000644 (NC_000013.11:g.32332434_32332435insA, NM_000059.3:c.956_957insA (BRCA2))
Individual ID |
00000117 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32332434_32332435insA |
Published as |
- |
Reference |
Hanis Nazihah Hasmad et al. (2016) |
DB-ID |
BRCA2_000093 |
dbSNP ID |
- |
Frequency |
1/3 |
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 |
2020-11-02 14:41:30 +08:00 (CST) |
Date last edited |
2020-12-03 09:25:06 +08:00 (CST) |

Variant on transcripts
Screenings
|
|