Variant #0000009249 (NC_000017.11:g.68522799G>A, NM_212471.3:c.221G>A (PRKAR1A))
Individual ID |
00001879 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.68522799G>A |
Reference |
- |
DB-ID |
PRKAR1A_000001 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2023-03-15 18:14:53 -03:00 (-03) |
Date last edited |
2023-05-08 14:45:07 -03:00 (-03) |
Variant on transcripts
Screenings
|
|