Variant #0000461193 (NC_000022.10:g.51064416T>C, NM_000487.5:c.1055A>G (ARSA))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.51064416T>C |
| DNA change (hg38) |
g.50625988T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ARSA_000009 See all 9 reported entries |
| Variant remarks |
cDNA expression cloning in BHK cells, no N-glycosylation (WB protein 2.5kDa smaller) but specific catalytic activity not affected |
| Reference |
PubMed: Gieselmann 1989 |
| ClinVar ID |
- |
| dbSNP ID |
rs2071421 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.16432 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2014-07-26 21:32:25 +02:00 (CEST) |
| Date last edited |
2020-07-17 16:20:13 +02:00 (CEST) |

Variant on transcripts
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