Variant #0000150694 (NC_000003.11:g.49135476C>A, NM_005051.1:c.2226G>T (QARS))
| Chromosome |
3 |
| Allele |
Unknown |
| 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.49135476C>A |
| DNA change (hg38) |
g.49098043C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
QARS_000007 |
| Variant remarks |
aAminoacylation activity reduced to 0.10 |
| Reference |
PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-12-16 19:58:43 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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