Variant #0000461205 (NC_000022.10:g.51064678C>T, NM_000487.5:c.883G>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.51064678C>T |
| DNA change (hg38) |
g.50626250C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ARSA_000024 See all 5 reported entries |
| Variant remarks |
0% residual activity |
| Reference |
PubMed: Berna 2004, Journal: Berna 2004, ExPASy_054194 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Martina Cesani |
| Database submission license |
No license selected |
| Created by |
Martina Cesani |
| Date created |
2014-07-31 18:02:06 +02:00 (CEST) |
| Date last edited |
2020-07-17 16:20:32 +02:00 (CEST) |

Variant on transcripts
|