Variant #0000505729 (NC_000001.10:g.227152778T>G, NM_020247.4:c.255T>G (ADCK3))

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.227152778T>G
DNA change (hg38) g.226965077T>G
Published as ADCK3(NM_020247.4):c.255T>G (p.H85Q, p.(His85Gln)), COQ8A(NM_020247.5):c.255T>G (p.H85Q)
ISCN -
DB-ID ADCK3_000009 See all 3 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) 0.01574 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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.255T>G r.(?) p.(His85Gln)


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