Variant #0000536376 (NC_000009.11:g.131085327G>A, NM_016035.3:c.103G>A (COQ4))

Chromosome 9
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.131085327G>A
DNA change (hg38) g.128323048G>A
Published as COQ4(NM_016035.5):c.103G>A (p.(Gly35Ser))
ISCN -
DB-ID COQ4_000013
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) 0.00018 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 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     
TRUB2 NM_015679.1 ?/. - c.-640C>T r.(?) p.(=)
COQ4 NM_016035.3 ?/. - c.103G>A r.(?) p.(Gly35Ser)


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