Variant #0000000342 (NC_000017.10:g.78188056A>G, NM_000199.3:c.578T>C (SGSH))
| Individual ID |
00000124 |
| Chromosome |
17 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78188056A>G |
| Reference |
- |
| DB-ID |
SGSH_000007 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Variome.ir |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Variome.ir |
| Date created |
2020-12-24 03:43:01 +00:00 (UTC) |
| Date last edited |
2020-12-24 03:45:30 +00:00 (UTC) |

Variant on transcripts
Screenings
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