Variant #0000008613 (NC_000011.10:g.108254034T>C, NM_000051.3:c.2119T>C (ATM))
Individual ID |
00001491 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Probably does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.108254034T>C |
Reference |
- |
DB-ID |
ATM_000078 See all 3 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Erika Stegmayer-CIOC |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-07 19:24:50 -02:00 (-02) |
Date last edited |
2020-11-07 19:25:13 -02:00 (-02) |
Variant on transcripts
Screenings
|
|