Variant #0000863626 (NC_000008.10:g.126163396_126163397insT, NC_000008.10(NM_173685.2):c.158-17_158-16insT (NSMCE2))
| Chromosome |
8 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.126163396_126163397insT |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
NSMCE2_000017 |
| Frequency |
4/12512 |
| Freq. EA |
3/8248 |
| Freq. AA |
1/4264 |
| 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 16:29:29 +02:00 (CEST) |
| Date last edited |
2013-05-04 15:36:22 +02:00 (CEST) |

Variant on transcripts
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