Variant #0000081416 (NC_000010.10:g.96741053A>C, NM_000771.3:c.1075A>C (CYP2C9))
Chromosome |
10 |
Allele |
Unknown |
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.96741053A>C |
DNA change (hg38) |
g.94981296A>C |
Published as |
- |
ISCN |
- |
DB-ID |
CYP2C9_000003 See all 58 reported entries |
Variant remarks |
expression cloning, catalytic efficiency 0.10 for S-warfarin, diclofenac and lauric acid |
Reference |
PubMed: Dickmann 2001 |
ClinVar ID |
- |
dbSNP ID |
rs1057910 |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.06361 View details |
Owner |
Johan den Dunnen |
Database submission license |
No license selected |
Created by |
Annemarie Schop (student) |
Date created |
2013-03-10 14:38:37 +01:00 (CET) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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