Variant #0000274336 (NC_000009.11:g.131094512G>C, NM_016035.3:c.483G>C (COQ4))

Chromosome 9
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.131094512G>C
DNA change (hg38) g.128332233G>C
Published as COQ4(NM_016035.3):c.483G>C (p.(Glu161Asp)), COQ4(NM_016035.4):c.483G>C (p.E161D)
ISCN -
DB-ID COQ4_000008 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) 0.00623 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COQ4 NM_016035.3 -/. - c.483G>C r.(?) p.(Glu161Asp)


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