Variant #0001925918 (NC_000022.10:g.37876196C>T, NC_000022.10(NM_002405.3):c.407+39G>A (MFNG))
| Chromosome |
22 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37876196C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
MFNG_000052 |
| Frequency |
20/13006 |
| Freq. EA |
19/8600 |
| Freq. AA |
1/4406 |
| 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 08:09:20 +02:00 (CEST) |

Variant on transcripts
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