Variant #0000081407 (NC_000010.10:g.96702047C>T, NM_000771.3:c.430C>T (CYP2C9))

Chromosome 10
Allele Unknown
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.96702047C>T
DNA change (hg38) g.94942290C>T
Published as -
ISCN -
DB-ID CYP2C9_000002 See all 72 reported entries
Variant remarks expression cloning, reduced rate of lauric acid metabolism
Reference PubMed: Crespi 1997
ClinVar ID -
dbSNP ID rs1799853
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.09261 View details
Owner Johan den Dunnen
Database submission license No license selected
Created by Annemarie Schop (student)
Date created 2013-03-05 11:12:43 +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 +?/. 3 c.430C>T r.(?) p.Arg144Cys -


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