Variant #0001055609 (NC_000016.9:g.57494516G>A, NM_020312.3:c.937G>A (COQ9))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57494516G>A
DNA change (hg38) -
Published as COQ9(NM_020312.4):c.937G>A (p.(Gly313Ser))
ISCN -
DB-ID CIAPIN1_000018
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) Retrieve
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     
DOK4 NM_018110.3 ?/. - c.*12773C>T r.(=) p.(=)
COQ9 NM_020312.3 ?/. - c.937G>A r.(?) p.(Gly313Ser)
CIAPIN1 NM_020313.2 ?/. - c.-13318C>T r.(?) p.(=)
POLR2C NM_032940.2 ?/. - c.-2121G>A r.(?) p.(=)


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