Variant #0000914213 (NC_000014.8:g.74422599A>G, NM_182476.2:c.449A>G (COQ6))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74422599A>G
DNA change (hg38) -
Published as COQ6(NM_182476.3):c.449A>G (p.(His150Arg), p.H150R)
ISCN -
DB-ID COQ6_000026 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) 0.00061 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENTPD5 NM_001249.2 -?/. - c.*11032T>C r.(=) p.(=)
FAM161B NM_152445.2 -?/. - c.-5681T>C r.(?) p.(=)
COQ6 NM_182476.2 -?/. - c.449A>G r.(?) p.(His150Arg)


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