Variant #0000689820 (NC_000006.11:g.88258318T>C, NM_020320.3:c.442A>G (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.88258318T>C
DNA change (hg38) -
Published as RARS2(NM_020320.4):c.442A>G (p.T148A), RARS2(NM_020320.5):c.442A>G (p.(Thr148Ala), p.T148A)
ISCN -
DB-ID RARS2_000005 See all 8 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) 0.00054 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RARS2 NM_020320.3 ?/. - c.442A>G r.(?) p.(Thr148Ala)


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