Variant #0000505740 (NC_000001.10:g.227170697C>T, NM_020247.4:c.1042C>T (ADCK3))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.227170697C>T
DNA change (hg38) g.226982996C>T
Published as ADCK3(NM_020247.4):c.1042C>T (p.(Arg348*)), COQ8A(NM_020247.4):c.1042C>T (p.R348*), COQ8A(NM_020247.5):c.1042C>T (p.R348*)
ISCN -
DB-ID ADCK3_000017 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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
ADCK3 NM_020247.4 +/. - c.1042C>T r.(?) p.(Arg348Ter)


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