Variant #0000200432 (NC_000002.11:g.229986T>C, NM_015677.2:c.761A>G (SH3YL1))
| Chromosome |
2 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.229986T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
SH3YL1_000022 |
| Frequency |
17/11946 |
| Freq. EA |
17/8214 |
| Freq. AA |
0/3732 |
| 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 16:22:05 +02:00 (CEST) |
| Date last edited |
2014-05-03 19:45:41 +02:00 (CEST) |

Variant on transcripts
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