Variant #0000306764 (NC_000006.11:g.88228353G>T, NM_020320.3:c.1410C>A (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.88228353G>T
DNA change (hg38) g.87518635G>T
Published as RARS2(NM_020320.4):c.1410C>A (p.L470=), RARS2(NM_020320.5):c.1410C>A (p.(Leu470=))
ISCN -
DB-ID RARS2_000012 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) 0.00181 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RARS2 NM_020320.3 -?/. - c.1410C>A r.(?) p.(Leu470=)


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