Variant #0000311427 (NC_000001.10:g.33276595C>T, NM_003680.3:c.121G>A (YARS))

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.33276595C>T
DNA change (hg38) g.32810994C>T
Published as YARS1(NM_003680.4):c.121G>A (p.G41R)
ISCN -
DB-ID YARS_000001 See all 2 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YARS NM_003680.3 +/. - c.121G>A r.(?) p.(Gly41Arg)
S100PBP NM_022753.3 +/. - c.-6815C>T r.(?) p.(=)


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