Variant #0000009792 (NC_000017.11:g.61684054_61684055del, NM_032043.2:c.2992_2993del (BRIP1))
Individual ID |
00002631 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.61684054_61684055del |
Reference |
- |
DB-ID |
BRIP1_000025 |
dbSNP ID |
rs878855151 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2024-01-17 14:44:28 -02:00 (-02) |
Date last edited |
N/A |
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Variant on transcripts
Screenings
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