Variant #0000200431 (NC_000002.11:g.229946A>G, NC_000002.11(NM_015677.2):c.781+20T>C (SH3YL1))
Chromosome |
2 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.229946A>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SH3YL1_000021 |
Frequency |
1/11866 |
Freq. EA |
1/8202 |
Freq. AA |
0/3664 |
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 |
2014-05-20 20:05:21 +02:00 (CEST) |

Variant on transcripts
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