Variant #0000604995 (NC_000001.10:g.173795858dup, NM_018122.4:c.161dup (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.173795858dup
DNA change (hg38) g.173826720dup
Published as DARS2(NM_018122.4):c.161dup (p.(Cys54TrpfsTer45))
ISCN -
DB-ID CENPL_000011
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DARS2 NM_018122.4 ?/. - c.161dup r.(?) p.(Cys54TrpfsTer45)
CENPL NM_033319.3 ?/. - c.-2684dup r.(?) p.(=)


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