Variant #0000716998 (NC_000001.10:g.173799885G>C, NM_018122.4:c.382G>C (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.173799885G>C
DNA change (hg38) -
Published as DARS2(NM_018122.5):c.382G>C (p.G128R)
ISCN -
DB-ID CENPL_000013
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.382G>C r.(?) p.(Gly128Arg)
CENPL NM_033319.3 +?/. - c.-6711C>G r.(?) p.(=)


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