Variant #0000000222 (NC_000023.10:g.148564365A>G, NM_000202.5:c.1565T>C (IDS))
| Individual ID |
00000016 |
| Chromosome |
X |
| Allele |
Maternal (inferred) |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Affects function |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.148564365A>G |
| Reference |
- |
| DB-ID |
IDS_000002 |
| 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 |
2020-12-17 21:13:24 +00:00 (UTC) |
| Date last edited |
2020-12-31 05:48:04 +00:00 (UTC) |

Variant on transcripts
Screenings
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