Variant #0000066633 (NC_000010.10:g.96824688C>T, NM_000770.3:c.511G>A (CYP2C8))

Chromosome 10
Allele Both (homozygous)
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.96824688C>T
DNA change (hg38) g.95064931C>T
Published as -
ISCN -
DB-ID CYP2C8_000006 See all 4 reported entries
Variant remarks cDNA expression cloning COS-1 cells shows normal expression level, normal 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) 0.0004 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 14:18:03 +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 -?/. 4 c.511G>A r.(?) p.Gly171Ser CYP2C8*6


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