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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WARS2 NM_015836.3 +/. - c.37T>G r.(?) p.(Trp13Gly)


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