Variant #0000461203 (NC_000022.10:g.51065110C>T, NM_000487.5:c.763G>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.51065110C>T |
| DNA change (hg38) |
g.50626682C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ARSA_000021 See all 6 reported entries |
| Variant remarks |
6.7% residual activity |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Martina Cesani |
| Database submission license |
No license selected |
| Created by |
Martina Cesani |
| Date created |
2014-07-31 16:30:22 +02:00 (CEST) |
| Date last edited |
2020-07-17 16:20:42 +02:00 (CEST) |

Variant on transcripts
|