Variant #0000091274 (NC_000022.10:g.51064630C>T, NM_000487.5:c.931G>A (ARSA))
| Chromosome |
22 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.51064630C>T |
| DNA change (hg38) |
g.50626202C>T |
| Published as |
1574G>A G309S |
| ISCN |
- |
| DB-ID |
ARSA_000144 See all 9 reported entries |
| Variant remarks |
BHK cell cDNA expression cloning, normal targtting lysosomes, unstable, activity reduced to 0.13 |
| Reference |
PubMed: Kreysing 1993 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-03-25 15:52:31 +01:00 (CET) |
| Date last edited |
2020-07-17 16:20:24 +02:00 (CEST) |

Variant on transcripts
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