Variant #0001909979 (NC_000022.10:g.23540414T>G, NC_000022.10(NM_004327.3):c.1279+15988T>G (BCR))
| Chromosome |
22 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23540414T>G |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
BCR_000056 |
| Frequency |
1641/5734 |
| Freq. EA |
1053/3982 |
| Freq. AA |
588/1752 |
| 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 16:50:05 +02:00 (CEST) |
| Date last edited |
2013-05-06 07:28:06 +02:00 (CEST) |

Variant on transcripts
|
|