Variant #0001031491 (NC_000001.10:g.173800759C>G, NM_018122.4:c.483C>G (DARS2))

Chromosome 1
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.173800759C>G
DNA change (hg38) -
Published as DARS2(NM_018122.5):c.483C>G (p.(Asn161Lys))
ISCN -
DB-ID CENPL_000028
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) 6.0E-5 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     
DARS2 NM_018122.4 ?/. - c.483C>G r.(?) p.(Asn161Lys)
CENPL NM_033319.3 ?/. - c.-7585G>C r.(?) p.(=)


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