Variant #0000536373 (NC_000009.11:g.131083973C>T, NM_016035.3:c.-1165C>T (COQ4))

Chromosome 9
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.131083973C>T
DNA change (hg38) g.128321694C>T
Published as TRUB2(NM_015679.1):c.146G>A (p.(Arg49His))
ISCN -
DB-ID COQ4_000010
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 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRUB2 NM_015679.1 -?/. - c.146G>A r.(?) p.(Arg49His)
COQ4 NM_016035.3 -?/. - c.-1165C>T r.(?) p.(=)


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