Variant #0000003081 (NC_000022.11:g.28695710C>T, NM_007194.3:c.1259G>A (CHEK2))
Individual ID |
00000382 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28695710C>T |
Reference |
- |
DB-ID |
CHEK2_000008 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Rita Valdez-Hospital Alemán |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2018-01-02 17:10:54 -02:00 (-02) |
Date last edited |
2023-04-28 15:24:37 -03:00 (-03) |
Variant on transcripts
Screenings
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