Variant #0000066709 (NC_000010.10:g.96798749T>C, NM_000770.3:c.1196A>G (CYP2C8))

Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.96798749T>C
DNA change (hg38) g.95038992T>C
Published as -
ISCN -
DB-ID CYP2C8_001007 See all 10 reported entries
Variant remarks cDNA expression cloning HepG2 cells shows reduced protein expression (normal RNA) and reduced values for Vmax and clearance
Reference PubMed: Soyama 2001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.08382 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2015-05-21 14:17:39 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2C8 NM_000770.3 +?/. 8 c.1196A>G r.(?) p.Lys399Arg -


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