Variant #0000008529 (NC_000017.11:g.61716051G>A, NM_032043.2:c.2392C>T (BRIP1))
Individual ID |
00001504 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.61716051G>A |
Reference |
- |
DB-ID |
BRIP1_000016 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Silvina Sisterna-Hospital de Comunidad |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-01 19:17:50 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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