Variant #0001054968 (NC_000014.8:g.100801283G>A, NM_004184.3:c.1345C>T (WARS))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.100801283G>A
DNA change (hg38) -
Published as WARS(NM_004184.4):c.1345C>T (p.(Arg449Cys))
ISCN -
DB-ID SLC25A47_000004
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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WARS NM_004184.3 ?/. - c.1345C>T r.(?) p.(Arg449Cys)
SLC25A47 NM_207117.2 ?/. - c.*5301G>A r.(=) p.(=)


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