Variant #0001053352 (NC_000009.11:g.131088128G>A, NM_016035.3:c.370G>A (COQ4))

Chromosome 9
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.131088128G>A
DNA change (hg38) -
Published as COQ4(NM_016035.5):c.370G>A (p.(Gly124Ser))
ISCN -
DB-ID COQ4_000029 See all 18 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) 0.00011 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
TRUB2 NM_015679.1 +/. - c.-3441C>T r.(?) p.(=)
COQ4 NM_016035.3 +/. - c.370G>A r.(?) p.(Gly124Ser)


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