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
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