Variant #0000005221 (NC_000017.11:g.61849248C>T, NM_032043.2:c.388G>A (BRIP1))
Individual ID |
00000669 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.61849248C>T |
Reference |
- |
DB-ID |
BRIP1_000008 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Hospital Alemán |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2018-10-31 12:10:45 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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