Variant #0000066707 (NC_000010.10:g.96798735G>C, NM_000770.3:c.1210C>G (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.96798735G>C |
| DNA change (hg38) |
g.95038978G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CYP2C8_001022 See all 3 reported entries |
| Variant remarks |
cDNA expression cloning HepG2 cells shows reduced protein expression (RNA normal) and significantly reduced clearance (normal Km) |
| 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) |
Retrieve |
| 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 13:52:39 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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