Variant #0000009803 (NC_000013.11:g.48303971C>T, NM_000321.2:c.59C>T (RB1))
Individual ID |
00002639 |
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.48303971C>T |
Reference |
- |
DB-ID |
RB1_000006 |
dbSNP ID |
rs587778637 |
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 |
2024-01-18 14:59:58 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
|
|