Variant #0000461195 (NC_000022.10:g.51065803G>A, NM_000487.5:c.256C>T (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.51065803G>A |
| DNA change (hg38) |
g.50627375G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ARSA_000008 See all 14 reported entries |
| Variant remarks |
6% 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 |
2014-07-27 16:35:45 +02:00 (CEST) |
| Date last edited |
2020-07-17 16:21:51 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|