Variant #0000321129 (NC_000001.10:g.173797451T>C, NC_000001.10(NM_018122.4):c.228-20T>C (DARS2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.173797451T>C
DNA change (hg38) g.173828313T>C
Published as DARS2(NM_018122.4):c.228-20delinsC (p.(=)), DARS2(NM_018122.5):c.228-20T>C
ISCN -
DB-ID DARS2_000002 See all 7 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) 0.27229 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DARS2 NM_018122.4 -/. - c.228-20T>C r.(=) p.(=)
CENPL NM_033319.3 -/. - c.-4277A>G r.(?) p.(=)


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