Variant #0000009490 (NC_000022.11:g.28725099A>G, NM_007194.3:c.470T>C (CHEK2))
Individual ID |
00002274 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28725099A>G |
Reference |
- |
DB-ID |
CHEK2_000045 See all 4 reported entries |
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 |
2023-04-18 17:08:27 -03:00 (-03) |
Date last edited |
N/A |
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Variant on transcripts
Screenings
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