Variant #0000009239 (NC_000022.11:g.28725338T>C, NM_001005735.1:c.478A>G (CHEK2))
Individual ID |
00001866 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28725338T>C |
Reference |
- |
DB-ID |
CHEK2_000022 See all 6 reported entries |
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 13:18:41 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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