Variant #0001065082 (NC_000011.9:g.9025295_9025296insG, NC_000011.9(NM_020645.2):c.174+13_174+14insC (NRIP3))
| Chromosome |
11 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.9025295_9025296insG |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
NRIP3_000053 |
| Frequency |
91/9130 |
| Freq. EA |
52/6170 |
| Freq. AA |
39/2960 |
| 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 16:37:25 +02:00 (CEST) |
| Date last edited |
2013-05-04 21:51:01 +02:00 (CEST) |

Variant on transcripts
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