Variant #0001015166 (NC_000014.8:g.74422201C>T, NM_182476.2:c.346C>T (COQ6))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74422201C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID COQ6_000030
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) 0.00019 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENTPD5 NM_001249.2 ?/. - c.*11430G>A r.(=) p.(=)
FAM161B NM_152445.2 ?/. - c.-5283G>A r.(?) p.(=)
COQ6 NM_182476.2 ?/. - c.346C>T r.(?) p.(Arg116Trp)


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