Variant #0001532358 (NC_000017.10:g.904231_904234del, NC_000017.10(NM_013337.2):c.509-21_509-18del (TIMM22))
| Chromosome |
17 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.904231_904234del |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
TIMM22_000043 |
| Frequency |
32/12518 |
| Freq. EA |
20/8254 |
| Freq. AA |
12/4264 |
| 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 16:44:12 +02:00 (CEST) |
| Date last edited |
2013-05-05 15:21:51 +02:00 (CEST) |

Variant on transcripts
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