Variant #0001052372 (NC_000006.11:g.44270223G>A, NM_020745.3:c.2392C>T (AARS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44270223G>A
DNA change (hg38) -
Published as AARS2(NM_020745.4):c.2392C>T (p.(Gln798*))
ISCN -
DB-ID TCTE1_000008
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 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AARS2 NM_020745.3 +?/. - c.2392C>T r.(?) p.(Gln798*)
TCTE1 NM_182539.3 +?/. - c.-4921C>T r.(?) p.(=)


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