Variant #0000252630 (NC_000016.9:g.57484950A>G, NC_000016.9(NM_020312.3):c.74-2A>G (COQ9))

Chromosome 16
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.57484950A>G
DNA change (hg38) g.57451038A>G
Published as COQ9(NM_020312.4):c.74-2A>G
ISCN -
DB-ID COQ9_000003
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 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COQ9 NM_020312.3 +/. - c.74-2A>G r.spl? p.?
CIAPIN1 NM_020313.2 +/. - c.-3752T>C r.(?) p.(=)


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