Variant #0001925900 (NC_000022.10:g.37873033_37873034insG, NC_000022.10(NM_002405.3):c.562-15_562-14insC (MFNG))
| Chromosome |
22 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37873033_37873034insG |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
MFNG_000034 |
| Frequency |
1/12518 |
| Freq. EA |
1/8254 |
| Freq. AA |
0/4264 |
| 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 16:50:05 +02:00 (CEST) |
| Date last edited |
2013-05-06 08:09:15 +02:00 (CEST) |

Variant on transcripts
|
|