Variant #0000002901 (NC_000022.11:g.28694066G>A, NM_007194.3:c.1427C>T (CHEK2))
Individual ID |
00000361 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28694066G>A |
Reference |
- |
DB-ID |
CHEK2_000006 See all 3 reported entries |
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 |
2017-12-22 14:55:02 -02:00 (-02) |
Date last edited |
2017-12-25 16:25:00 -02:00 (-02) |
Variant on transcripts
Screenings
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