Variant #0000323754 (NC_000014.8:g.74416832G>T, NM_182476.2:c.-204G>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.74416832G>T
DNA change (hg38) g.73950129G>T
Published as COQ6(NM_182476.2):c.-204G>T (p.(=)), COQ6(NM_182480.2):c.37G>T (p.V13F)
ISCN -
DB-ID COQ6_000013 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) 0.00237 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM161B NM_152445.2 ?/. - c.87C>A r.(?) p.(Asp29Glu)
COQ6 NM_182476.2 ?/. - c.-204G>T r.(?) p.(=)


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