Variant #0000552968 (NC_000014.8:g.74424938T>C, NM_182476.2:c.570T>C (COQ6))

Chromosome 14
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.74424938T>C
DNA change (hg38) g.73958235T>C
Published as COQ6(NM_182480.3):c.495T>C (p.H165=)
ISCN -
DB-ID COQ6_000010 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) 0.33602 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENTPD5 NM_001249.2 -/. - c.*8693A>G r.(=) p.(=)
FAM161B NM_152445.2 -/. - c.-8020A>G r.(?) p.(=)
COQ6 NM_182476.2 -/. - c.570T>C r.(?) p.(His190=)


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