Variant #0000893099 (NC_000016.9:g.57493591C>T, NM_020312.3:c.826C>T (COQ9))

Chromosome 16
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.57493591C>T
DNA change (hg38) -
Published as COQ9(NM_020312.3):c.826C>T (p.R276W), COQ9(NM_020312.4):c.826C>T (p.R276W)
ISCN -
DB-ID COQ9_000006 See all 4 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) 0.00405 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 2022-11-01 13:41:49 +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.*13698G>A r.(=) p.(=)
COQ9 NM_020312.3 -?/. - c.826C>T r.(?) p.(Arg276Trp)
CIAPIN1 NM_020313.2 -?/. - c.-12393G>A r.(?) p.(=)
POLR2C NM_032940.2 -?/. - c.-3046C>T r.(?) p.(=)


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