Variant #0000009190 (NC_000011.10:g.108253814T>G, NM_000051.3:c.1899T>G (ATM))
Individual ID |
00001861 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.108253814T>G |
Reference |
- |
DB-ID |
ATM_000027 See all 3 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 |
2021-12-03 15:51:06 -02:00 (-02) |
Date last edited |
2021-12-03 15:53:10 -02:00 (-02) |
Variant on transcripts
Screenings
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