Variant #0000621782 (NC_000006.11:g.88240519A>T, NM_020320.3:c.754T>A (RARS2))

Chromosome 6
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.88240519A>T
DNA change (hg38) g.87530801A>T
Published as RARS2(NM_001350508.1):c.229T>A (p.Y77N), RARS2(NM_020320.5):c.754T>A (p.(Tyr252Asn))
ISCN -
DB-ID RARS2_000047 See all 3 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) 0.00021 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RARS2 NM_020320.3 ?/. - c.754T>A r.(?) p.(Tyr252Asn)


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