Variant #0001006626 (NC_000010.10:g.88722322T>C, NC_000010.10(NM_003087.2):c.292-39T>C (SNCG))
| Chromosome |
10 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88722322T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
SNCG_000026 |
| Frequency |
1/12996 |
| Freq. EA |
1/8596 |
| Freq. AA |
0/4400 |
| 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 16:30:47 +02:00 (CEST) |
| Date last edited |
2013-05-04 19:55:37 +02:00 (CEST) |

Variant on transcripts
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