Variant #0000009538 (NC_000003.12:g.52406289C>A, NM_004656.3:c.747G>T (BAP1))
Individual ID |
00002241 |
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.52406289C>A |
Reference |
- |
DB-ID |
BAP1_000010 |
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 |
2023-05-05 14:45:18 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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