Variant #0000066635 (NC_000010.10:g.96824643G>A, NM_000770.3:c.556C>T (CYP2C8))

Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.96824643G>A
DNA change (hg38) g.95064886G>A
Published as -
ISCN -
DB-ID CYP2C8_000007 See all 4 reported entries
Variant remarks cDNA expression cloning COS-1 cells gives undetectable protein, no paclitaxel 6alpha-hydroxylation activity
Reference PubMed: Hichiya 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00024 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 2015-05-18 14:59:37 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2C8 NM_000770.3 +/. 4 c.556C>T r.(?) p.Arg186* CYP2C8*7


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.