Variant #0000264969 (NC_000016.9:g.57493629G>C, NM_020312.3:c.864G>C (COQ9))

Chromosome 16
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.57493629G>C
DNA change (hg38) g.57459717G>C
Published as COQ9(NM_020312.4):c.864G>C (p.K288N)
ISCN -
DB-ID COQ9_000007
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) 0.00413 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 2018-01-15 20:58:59 +01:00 (CET)
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     
DOK4 NM_018110.3 -/. - c.*13660C>G r.(=) p.(=)
COQ9 NM_020312.3 -/. - c.864G>C r.(?) p.(Lys288Asn)
CIAPIN1 NM_020313.2 -/. - c.-12431C>G r.(?) p.(=)
POLR2C NM_032940.2 -/. - c.-3008G>C r.(?) p.(=)


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