Variant #0000944862 (NC_000001.10:g.119683231A>C, NM_015836.3:c.37T>G (WARS2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (!) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.119683231A>C |
| DNA change (hg38) |
g.119140608A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
WARS2_000007 See all 15 reported entries |
| Variant remarks |
hypomorphic variant; 6 apparently healthy homozygous carriers in gnomAD; to date all individuals with a childhood- or early adulthood-onset movement disorder have this hypomorphic in trans with a WARS2 pathogenic variant |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00322 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-11-15 14:07:58 +01:00 (CET) |
| Date last edited |
2023-11-16 21:21:13 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|