Variant #0001120362 (NC_000011.9:g.69458033C>G, NC_000011.9(NM_053056.2):c.414+19C>G (CCND1))
| Chromosome |
11 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.69458033C>G |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CCND1_000018 |
| Frequency |
7/12332 |
| Freq. EA |
0/8186 |
| Freq. AA |
7/4146 |
| Average frequency (gnomAD v.2.1.1) |
- |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Ivo F.A.C. Fokkema |
| Date created |
2013-05-03 16:37:25 +02:00 (CEST) |
| Date last edited |
2013-05-04 23:38:10 +02:00 (CEST) |

Variant on transcripts
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