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 International |
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) |

Variant on transcripts
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