Variant #0001035960 (NC_000006.11:g.88240547T>C, NM_020320.3:c.726A>G (RARS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88240547T>C
DNA change (hg38) -
Published as RARS2(NM_001350508.1):c.201A>G (p.Q67=), RARS2(NM_020320.5):c.726A>G (p.(Gln242=))
ISCN -
DB-ID RARS2_000059 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) 0.00064 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 2025-05-05 21:14:00 +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     
RARS2 NM_020320.3 -?/. - c.726A>G r.(?) p.(Gln242=)


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