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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2C9 NM_000771.3 +/. 7 c.1075A>C r.(?) p.Ile359Leu -


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