Variant #0000891382 (NC_000009.11:g.21971038C>T, NM_000077.4:c.320G>A (CDKN2A))
| Chromosome |
9 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21971038C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CDKN2A_000022 |
| Frequency |
1/12970 |
| Freq. EA |
1/8576 |
| Freq. AA |
0/4394 |
| 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 16:29:58 +02:00 (CEST) |
| Date last edited |
2013-05-04 16:24:19 +02:00 (CEST) |

Variant on transcripts
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