Variant #0000504299 (NC_000001.10:g.173797461dup, NC_000001.10(NM_018122.4):c.228-10dup (DARS2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.173797461dup
DNA change (hg38) g.173828323dup
Published as DARS2(NM_018122.4):c.228-10dup (p.(=))
ISCN -
DB-ID CENPL_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.228-10dup r.(=) p.(=)
CENPL NM_033319.3 -?/. - c.-4278dup r.(?) p.(=)


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