Variant #0000002199 (NC_000013.11:g.32363403C>T, NM_000059.3:c.8201C>T (BRCA2))
Individual ID |
00000414 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.32363403C>T |
Published as |
- |
Reference |
Wei Xiong Wen et al. (2018), dbSNP, ClinVar |
DB-ID |
BRCA2_000157 |
dbSNP ID |
rs876658732 |
Frequency |
1/1726 |
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 12:46:43 +08:00 (CST) |
Date last edited |
2021-08-01 12:47:52 +08:00 (CST) |

Variant on transcripts
Screenings
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