Variant #0000270677 (NC_000001.10:g.173797459C>G, NC_000001.10(NM_018122.4):c.228-12C>G (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.173797459C>G
DNA change (hg38) g.173828321C>G
Published as DARS2(NM_018122.4):c.228-12C>G (p.(=)), DARS2(NM_018122.5):c.228-12C>G
ISCN -
DB-ID DARS2_000039 See all 4 reported entries
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) 0.0213 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.228-12C>G r.(=) p.(=)
CENPL NM_033319.3 -?/. - c.-4285G>C r.(?) p.(=)


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