Variant #0000009504 (NC_000022.11:g.28694026A>G, NC_000022.11(NM_007194.3):c.1461+6T>C (CHEK2))
Individual ID |
00001871 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28694026A>G |
Reference |
- |
DB-ID |
CHEK2_000050 |
dbSNP ID |
- |
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 |
2023-04-19 18:17:55 -03:00 (-03) |
Date last edited |
N/A |
![Options](gfx/options_button.png)
Variant on transcripts
Screenings
|
|