Variant #0000008627 (NC_000022.11:g.28734565A>T, NM_001005735.1:c.157T>A (CHEK2))
Individual ID |
00001521 |
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.28734565A>T |
Reference |
- |
DB-ID |
CHEK2_000027 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Norma Rossi-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-07 20:48:16 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
|
|