Variant #0000009428 (NC_000011.10:g.108312467A>C, NM_000051.3:c.5975A>C (ATM))
Individual ID |
00002186 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.108312467A>C |
Reference |
- |
DB-ID |
ATM_000111 See all 2 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Silvina Sisterna-Hospital de Comunidad |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2023-04-13 16:29:15 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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