Variant #0000857318 (NC_000001.10:g.227170603C>T, NM_020247.4:c.948C>T (ADCK3))

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.227170603C>T
DNA change (hg38) -
Published as COQ8A(NM_020247.4):c.948C>T (p.L316=), COQ8A(NM_020247.5):c.948C>T (p.L316=)
ISCN -
DB-ID ADCK3_000049 See all 2 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) 0.0022 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADCK3 NM_020247.4 -?/. - c.948C>T r.(?) p.(Leu316=)


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