Variant #0000461189 (NC_000022.10:g.51066047A>G, NM_000487.5:c.161T>C (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.51066047A>G |
DNA change (hg38) |
g.50627619A>G |
Published as |
- |
ISCN |
- |
DB-ID |
ARSA_000005 |
Variant remarks |
<1% residual activity |
Reference |
PubMed: Cesani 2009, Journal: Cesani 2009, ExPASy_067414 |
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 |
2014-07-22 11:52:21 +02:00 (CEST) |
Date last edited |
2020-07-17 16:21:58 +02:00 (CEST) |

Variant on transcripts
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