Variant #0000454338 (NC_000010.10:g.96702047C>T, NM_000771.3:c.430C>T (CYP2C9))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
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 -
Reference -
ClinVar ID -
dbSNP ID rs1057910
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.09261 View details
Owner Hye Sun Gwak
Database submission license No license selected
Created by Hye Sun Gwak
Date created 2019-01-28 09:42:29 +01:00 (CET)
Date last edited 2019-02-26 16:57:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
CYP2C9 NM_000771.3 ?/. - c.430C>T r.(?) p.(Arg144Cys) -



Screenings

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