Variant #0000558605 (NC_000016.9:g.57494029C>T, NC_000016.9(NM_020312.3):c.921+13C>T (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.57494029C>T
DNA change (hg38) g.57460117C>T
Published as COQ9(NM_020312.4):c.921+13C>T
ISCN -
DB-ID CIAPIN1_000009 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) 0.00291 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DOK4 NM_018110.3 -/. - c.*13260G>A r.(=) p.(=)
COQ9 NM_020312.3 -/. - c.921+13C>T r.(=) p.(=)
CIAPIN1 NM_020313.2 -/. - c.-12831G>A r.(?) p.(=)
POLR2C NM_032940.2 -/. - c.-2608C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.