Variant #0000461197 (NC_000022.10:g.51065436G>T, NM_000487.5:c.510C>A (ARSA))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.51065436G>T |
| DNA change (hg38) |
g.50627008G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ARSA_000016 See all 2 reported entries |
| Variant remarks |
0% residual activity |
| Reference |
Journal: Cesani et al. (2009) |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Martina Cesani |
| Database submission license |
No license selected |
| Created by |
Martina Cesani |
| Date created |
2014-07-30 18:56:14 +02:00 (CEST) |
| Date last edited |
2020-07-17 16:21:09 +02:00 (CEST) |

Variant on transcripts
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