Variant #0000926312 (NC_000016.9:g.57484957C>G, NM_020312.3:c.79C>G (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.57484957C>G
DNA change (hg38) -
Published as COQ9(NM_020312.4):c.79C>G (p.R27G)
ISCN -
DB-ID COQ9_000004 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) 0.00226 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COQ9 NM_020312.3 -/. - c.79C>G r.(?) p.(Arg27Gly)
CIAPIN1 NM_020313.2 -/. - c.-3759G>C r.(?) p.(=)


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