Variant #0001063212 (NC_000001.10:g.173795900del, NM_018122.4:c.203del (DARS2))

Chromosome 1
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.173795900del
DNA change (hg38) -
Published as DARS2(NM_018122.5):c.203del (p.(Leu68Cysfs*16))
ISCN -
DB-ID CENPL_000032
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +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     
DARS2 NM_018122.4 +?/. - c.203del r.(?) p.(Leu68Cysfs*16)
CENPL NM_033319.3 +?/. - c.-2725del r.(?) p.(=)


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