Variant #0000001942 (NC_000017.11:g.61686104T>C, NM_032043.2:c.2637A>G (BRIP1))
Individual ID |
00000184 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Probably does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.61686104T>C |
Reference |
- |
DB-ID |
BRIP1_000001 See all 28 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Alejandra Mampel-Hospital Universitario de Mendoza |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2017-07-21 12:40:32 -03:00 (-03) |
Date last edited |
2018-01-15 14:16:04 -02:00 (-02) |
Variant on transcripts
Screenings
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