Variant #0000006394 (NC_000022.11:g.28687974G>A, NM_007194.3:c.1555C>T (CHEK2))
Individual ID |
00000980 |
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.28687974G>A |
Reference |
- |
DB-ID |
CHEK2_000024 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Hospital Alemán |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-01-13 11:35:23 -02:00 (-02) |
Date last edited |
N/A |
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Variant on transcripts
Screenings
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