Variant #0001004192 (NC_000018.9:g.55273918T>G, NM_004539.3:c.1067A>C (NARS))

Chromosome 18
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.55273918T>G
DNA change (hg38) -
Published as NARS(NM_004539.3):c.1067A>C (p.(Asp356Ala)), NARS1(NM_004539.4):c.1067A>C (p.D356A)
ISCN -
DB-ID NARS_000011 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00095 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NARS NM_004539.3 +/. - c.1067A>C r.(?) p.(Asp356Ala)


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