Variant #0000150695 (NC_000003.11:g.49137195G>A, NM_005051.1:c.1387C>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.49137195G>A
DNA change (hg38) g.49099762G>A
Published as -
ISCN -
DB-ID QARS_000005 See all 3 reported entries
Variant remarks aminoacylation activity reduce to 0.00
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) 2.0E-5 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 2016-12-16 20:00:16 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QARS NM_005051.1 +/. 15 c.1387C>T r.(?) p.Arg463*


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