Variant #0000005531 (NC_000011.10:g.108248927T>G, NC_000011.10(NM_000051.3):c.1066-6T>G (ATM))
Individual ID |
00000768 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.108248927T>G |
Reference |
- |
DB-ID |
ATM_000030 See all 2 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 |
2019-02-15 16:24:29 -02:00 (-02) |
Date last edited |
2023-04-27 15:57:15 -03:00 (-03) |
Variant on transcripts
Screenings
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